p-BLOCK ELEMENTS

p-BLOCK ELEMENTS
GROUP 15 ELEMENTS : THE NITROGEN FAMILY
Group 15 includes nitrogen phosphorus, arsenic, antimony and bismuth. As we go down the group, there is a shift from non-
metallic to metallic through metalloidic character. Nitrogen and phosphorus are non-metal, arsenic and antimony metalloid
and bismuth is a typical metal.
Electronic Configuration :
The valence shell electronic configuration of these element is ns2 np3 the s orbital in these element is completely filled and
p orbitals are half- filled, making their electronic configuration extra stable.
Atomic and Ionic Radii :
Covalent and ionic (in a particular state) radii increase in size down the group. There is a considerable increase in covalent
radius from N to P. However, from As to Bi only a small increase in covalent radius is observed. This is due to the presence
of completely filled d and / or f orbitals in heavier members.
Ionisation Enthalpy:
Ionisation enthalpy decreases down the group due to gradual increase in atomic size. Because of the extra stable half- filled
p-orbital electronic configuration and smaller size, the ionisation enthaply of the group 15 element is much greater
than of group 14 elements in the corresponding periods. The order of successive ionisation enthalpies, as expected is
iH1 < iH2 < iH3
Electronegativity :
The electronegativity value, in general, decreases down the group with increasing atomic size. However, amongst the heavier
elements, the difference is not that much pronounced.
Physical Properties:
All the elements of this group are polyatomic. Dinitrogen is a diatomic gas while all others are solids. Metallic character
increases down the group. Nitrogen and phosphours are non – metals , arsenic and antimony metalloids and bismuth is a
metal. This is due to decrease in ionisation enthalpy and increase in atomic size. The boiling points , in general , increase
from top to bottom in the group but the melting point increases upto arsenic and then decreases upto bismuth. Except
nitrogen , all the elements show allotropy.
ATOMIC & PHYSICAL PROPERTIES

Element N P As Sb Bi
Atomic Number 7 15 33 51 83
Atomic Mass 14.01 30.97 74.92 121.76 208.98
2 3 2 3 10 2 3 10 2 3 14
Electronic configuration [He] 2s 2p [Ne] 3s 3p [Ar] 3d 4s 4p [Kr] 4d 5s 5p [Xe] 4f 5d10 6s2 6p3
Covalent Radius / pm 70 110 120 140 150
Ionic Radius / pm
171a 212a 222a 76b 103b
a = M3–, b = M+3
 1402 1012 947 834 703
Ionization enthalpy
 2856 1903 1798 1595 1610
/ (kJ mol–1)
 4577 2910 2736 2443 2466
Electronegativity 3.0 2.1 2.0 1.9 1.9

Chemical Properties :
Oxidation States and trends in a chemical reactivity :
The common oxidation states of these elements are – 3 , + 3 and + 5. The tendency to exhibit – 3 oxidation state decreases
down the group , bismuth hardly forms any compound in –3 oxidation state. The stability of + 5 oxidation state decreases
down the group. The only well characterised Bi (V) compound is BiF5 .The stability of + 5 oxidation state decreases and that
of +3 state increases (due to inert pair effect) down the group. Nitrogen exhibits +1 , + 2 , + 4 oxidation states also when it
reacts with oxygen. Phosphours also shows + 1 and + 4 oxidation states in some oxoacids.
In the case of nitrogen , all oxidation states from +1 to +4 tend to disproportionate in acid solution. For example ,
3 HNO2  HNO3 + H2O + 2 NO
Similarly , in case of phosphorus nearly all intermediate oxidation states disproportionate into +5 and –3 both in alkali and
acid. However +3 oxidation state in case of arsenic , antimony and bismuth become increasingly stable with respect to
disproportionation.
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Nitrogen is restricted to a maximum covalency of 4 since only four (one s and three p) orbitals are available for bonding. The
heavier elements have vacant d orbitals in the outermost shell which can be used for bonding (covalency) and hence , expand
their covalence as in PF6– .
Anomalous properties of nitrogen :
Nitrogen differs from the rest of the members of this group due to its smaller size , high electronegativity , high ionisation
enthalpy and non – availability of d orbitals. Nitrogen has unique ability to form p – p multiple bonds with itself and with
other elements having small size and high electronegativity (e.g., C ,O). Heavier elements of this group do not form p – p
bonds as their atomic orbitals are so large and diffuse that they cannot have effective overlapping. Thus, nitrogen exists as a
diatomic molecule with a triple bond (one s and two p) between the two atoms. Consequently , its bond enthalpy (941.1 kJ
mol–1) is very high. On the contrary , phosphorus , arsenic and antimony form metallic bonds in elemental state. However ,
the single N – N bond is weaker than the single P – P bond because of high interelectronic repulsion of the non – bonding
electrons , owing to the small bond length. As a result the catenation tendency is weaker in nitrogen. Another factor which
affects the chemistry of nitrogen is the absence of d orbitals in its valence shell. Besides restricting its covalency to four ,
nitrogen cannot form d – p bonds as the heavier elements can e.g., R3P = O or R3P = CH2 (R = alkyl group). Phosphours
and arsenic can form d – p bond also with transition metals when their compounds like P(C2H5)3 and As(C6H5)3 act as
ligands.
(i) Reactivity towards hydrogen :
All the elements of Group 15 form hydrides of the type EH3 where E = N , P, As, Sb or Bi. Some of the properties of these
hydrides are shown in Table. The hydrides show regular gradation in their properties. The stability of hydrides decreases
from NH3 to BiH3 which can be observed from their bond dissociation enthalpy. Consequently , the reducing character of the
hydrides increases. Ammonia is only a mild reducing agent while BiH3 is the strongest reducing agent amongst all the
hydrides. Basicity also decreases in the order
NH3 > PH3 > AsH3 > SbH3  BiH3 .
Properties of Hydrides of Group 15 Elements

Property NH3 PH3 AsH3 SbH3 BiH3

Melting point / K 195.2 139.5 156.7 185 –

Boiling point / K 238.5 185.5 210.6 254.6 290
(E – H) Distance / pm 101.7 141.9 151.9 170.7 –
0
HEH angle ( ) 107.8 93.6 91.8 91.3 –
fH / kJ mol
– –1
– 46.1 13.4 66.4 145.1 278

dissH–(E – H) / kJ mol–1 389 322 297 255 –

(ii) Reactivity towards oxygen :

All these elements form two types of oxides : E2O3 and E2O5 . The oxide in the higher oxidation state of the element is more
acidic than that of lower oxidation state. Their acidic character decreases down the group. The oxides of the type E2O3 of
nitrogen and phosphours are purely acidic , that of arsenic and antimony amphoteric and those of bismuth is predominantly
basic.
(iii) Reactivity towards halogens :
These elements react to form two series of halides : EX3 and EX5 . Nitrogen does not form pentahalide due to non –
availability of the d – orbitals in its valence shell. Pentahalides are more covalent than trihalides. All the trihalides of these
elements except those of nitrogen are stable. In case of nitrogen , only NF3 is known to be stable. Trihalides except BiF3 are
predominantly covalent in nature.
(iv) Reactivity towards metals :
These elements react with metals to form their binary compounds exhibiting –3 oxidation state , such as , Ca 3N2 (calcium
nitride) Ca3P2 (calcium phosphide) , Na3As2 (sodium arsenide) , Zn3Sb2 (zinc antimonide) and Mg3Bi2 (magnesium
bismuthide).
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 NITROGEN (N):
 PREPARATION:
(i) By heating a mixture of NH4Cl and NaNO2. N2 is collected by the downward displacement of water.
 
NH4Cl + NaNO2  NH4NO2 + NaCl ; NH4NO2  N2 + 2H2O
* By treating an aqueous solution of ammonium chloride with sodium nitrate. It is laboratory method of preparation.
NH4Cl(aq) + NaNO2(aq)  N2(g) + H2O () + NaCl(aq)
(ii) By heating ammonium dichromate:

(NH4)2Cr2O7  N2  + 4H2O + Cr2O3
(iii) By oxidation of ammonia
(A) At lower temperature
(a) 8NH3 () + 3Cl2 (g)  6NH4Cl + N2 
If excess of Cl2 is used in this reaction, nitrogen trichloride is formed as per the following reaction,
NH3 + 3Cl2  NCl3 + 3HCl
Nitrogen trichloride is an explosive substance.
(b) By reation of ammonia with calcium hypochlorite or Br2
4NH3 + 3Ca(OCI)2  3CaCl2 + N2 + H2O
(B) At higher temperature
By passing ammonia over heated cupric oxide or PbO :
2NH3 + 3CuO  N2 + 3Cu + 3H2O
(iv) By heating urea with a nitrite in presence of dilute H2SO4:

NH2CONH2 + 2NaNO2 + H2SO4  Na2SO4 + 2N2 + 3H2O + CO2 
(v) By heating urea solution with sodium hypobromite:

NH2CONH2 + 3NaOBr  N2 + 3NaBr + 2H2O + CO2 
(vi) By passing nitric oxide and NH3 over red hot copper gauze:
4NH3 + 6NO  5N2 + 6H2O
(vii) By passing HNO3 vapours on red hot copper:
5Cu + 2HNO3  5CuO + N2 + H2O
Very pure nitrogen ; Ba(N3)2 
(viii)  Ba + 3N2
Sodium azide also gives N2 on heating.
INDUSTRIAL METHODS OF PREPARATION:
(i) From liquefied air by fractional distillation : The bp of N2 is –196oC and that of oxygen is –183oC and hence they
can be separated.
(ii) From producer gas from furnaces : Producer gas is a mixture of CO and N2. When the mixture of CO and N2 is
passed over heated CuO, the CO gas is oxidized to CO2 which is absorbed in alkalies & N2 remains which is
collected in gas cylinders.
 PROPERTIES:
(i) N2 is a colourless, odourless gas insoluble in water.
(ii) It is non-polar covalent and neutral molecule.
(iii) It is neither combustible nor a supporter of combustion.
(iv) It is absorbed by heated Mg and Al. The nitrides formed thus react with water to form NH3.
3Mg + N2  Mg3N2 (+ 6H2O)  3Mg(OH)3 + 2NH3 
2Al + N2  2AlN (+ 6H2O)  2Al(OH)3 + 2NH3
(v) Reaction with H2: At 200 atm and 500oC, and in the presence of iron catalyst and molybdenum promoter, N2
combines with H2 reversibly to form ammonia. The process is called Haber’s Process and is the industrial method
of manufacturing ammonia. The reaction is exothermic.
N2 + 3H2  2NH3
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(vi) Reaction with oxygen: When air free from CO2 and moisture is passed over an electric arc at about 2000 K,
nitric oxide is formed. This reaction is endothermic.
N2 + O2  2NO
(vii) Reaction with CaC2 and BaC2: At 1100oC, these carbides react with N2 forming CaCN2 and Ba(CN)2 respectively.
 
CaC2 + N2 +  CaCN2 + C (nitrolim, a fertilizer) ; BaC2 + N2 +  Ba(CN)2
CaCN2 reacts with H2O in the soil to produce NH3 gas. NH3 gas is converted by the nitrating bacteria present in soil
into nitrates. (The nitrates are readily absorbed by the plants and meet their requirement of the element nitrogen.)
 USES :
(i) for providing an inert atmosphere during many industrial processes where presence of air or O2 is to be avoided.
(ii) for manufacture of NH3 by the Haber’s process.
(iii) for manufacture of HNO3 by the Birkeland-Eyde process.
(iv) for manufacture of nitrolim.
 COMPOUNDS OF NITROGEN :
 AMMONIA :
 PREPARATION :
(i) By the action of any base or alkali on any ammonium salt :
 
NH4Cl + NaOH  NH3 + NaCl + H2O ; (NH4)2SO4 + 2NaOH  2NH3 + Na2SO4 + 2H2O
 
NH4NO3 + NaOH  NH3 + NaNO3 + H2O ; (NH4)3PO4 + 3NaOH  3NH3 + Na3PO4 + 3H2O

(NH4)2SO4 + CaO  2NH3 + CaSO4 + H2O
This is a general method and is used as a test for ammonium salts.
(ii) By the hydrolsis of metal nitrides like AlN or Mg3N2.
AlN + NaOH + H2O  NaAlO2 + NH3
(iii) From oxides of nitrogen: When oxides of nitrogen are mixed with H 2 and the mixture is
passed over heated platinum catalyst, NH3 gas is evolved.
2NO + 5H2  2NH3 + 2H2O ;2NO2 + 7H2  2NH3 + 4H2O
(iv) From organic amides: When an organic amide is heated with NaOH solution ammonia is
evolved.

CH3CONH2 + NaOH  CH3COONa + NH3
(v) From nitrates and nitrites: When a metal nitrate or nitrite is heated with zinc powder and
concentrated NaOH solution ammonia is obtained. The reactions are
NaNO3 + 7NaOH + 4Zn  4Na2ZnO2 + NH3 + 2H2O
NaNO2 + 3Zn + 5NaOH  3Na2ZnO2 + H2O + NH3
Thus a nitrite or a nitrate can be identified by this reaction but this test cannot make distinction between them.
 The ammonia evolved is passed through quick lime to dry it and collected by the downward displacement
of air. Ammonia cannot be dried using CaCl2, P2O5, or conc. H2SO4 because NH3 reacts with all of these.
CaCl2 + 8NH3  CaCl2·8NH3 ; P2O5 + 6NH3 + 3H2O  2(NH4)3PO4
H2SO4 +2NH3  (NH4)2SO4
CaO + H2O  Ca(OH)2
INDUSTRIAL METHODS OF PREPARATION:

Haber’s process : N2 + 3H2     2NH3

500 º C, 200 atm.
(i)
Iron oxide K 2O & Al 2O3

(ii) From destructive distillation of coal: When coal is heated at a high temperature in an iron retort and the
distillate is bubbles in water, three substances are obtained:
(a) Tarry black pitch, (b) Liquor ammonia & (c) Coal gas
The liquor ammonia is a concentrated solution of ammonia and ammonium salts. When heated it gives out ammonia. When
all the free NH3 is obtained, the residual liquid is heated with Ca(OH)2 when ammonium salts get decomposed to liberate
further quantity of ammonia.
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Cyanamide process: CaO + 2C + N2   CaCN2 + CO; CaCN2 + 3H2O  CaCO3 + 2NH3
2000 º C
(iii)

PROPERTIES:
(i) Colourless gas lighter than air. Being basic in nature turns red litmus blue. It acts as a Lewis base
(ii) Highly soluble in water. The solution is called ammonium hydroxide solution.
(iii) 
Na + NH3  NaNH2 + 1/2 H2
Amides decompose back with water to form NH3 and NaOH.
(iv) 4NH3 + 5O2    4NO + 6H2O (Ostwald’s process of manufacturing HNO3)
Pt , 550 º C

(v) When Cl2 is bubbled in liquor ammonia, nitrogen gas is formed.

8NH3 + 3Cl2  6NH4Cl + N2
With excess of Cl2 it is converted to an explosive substance, nitrogen trichloride.
NH3 + 3Cl2  NCl3 +3HCl
(vi) Cupric oxide and PbO are reduced to metal when NH3 is passed over heated CuO and PbO.
3CuO + 2NH3  3Cu + 3H2O + N2; 3PbO + 2NH3  3Pb + 3H2O + N2
(vii) CuSO4 + 2NH4OH  Cu(OH)2(blue) + (NH4)2SO4
Cu(OH)2 + (NH4)2SO4 + 3NH4OH (excess)  [Cu(NH3)4]SO4 (deep blue solution) + 4H2O
ZnSO4 + 2NH4OH  Zn(OH)2(white) + (NH4)2SO4
Zn(OH)2 + (NH4)2SO4 + 2NH4OH (excess)  [Zn(NH3)4] SO4 (colourless solution) + 4H2O
Similar reactions occur with CdSO4 solution also.
(viii) M(NO3)2 + 2NH4OH  M(OH)2 (white) + 2NH4NO3
MCl2 + 2NH4OH  M(OH)2(white) + 2NH4Cl
(M = Mg, Ca, Sr, Ba, Ra, Sn, Pb)
(ix) When NH4OH solution is added to AgNO3 solution, a brown ppt. is obtained
2AgNO3 + 2NH4OH  Ag2O (brown) + 2NH4NO3 + H2O
 Brown ppt of silver oxide formed dissolves in excess ammonium hydroxide forming a soluble complex
Ag2O + 2NH4OH  [Ag(NH3)2]OH (colourless solution) + 2H2O
Similarly with mercuric salts, NH4OH forms a white precipitate
HgCl2 (aq.) + 2NH4OH  HgNH2Cl (white) + NH4Cl + H2O
(x) When liquor ammonia is dropped on heated bleaching powder, nitrogen gas is formed
3Ca(OCl)Cl + 2NH3  3CaCl2 + 3H2O + N2

2NH3 + CO2 

 NH CONH (urea) + H O
high pressure
(xi) 2NH3 + CO2 + H2O  (NH4)2CO3 ; 2 2 2

(xii) When NH3 gas is passed into the colourless solution of Nessler’s reagent a brown precipitate or coloration is
formed. This is a test for NH3 gas.
2K2HgI4 + 3KOH + NH3  H2N·HgO·HgI (brown) + 7KI + 2H2O
(xiii)H2PtCl6 + 2NH4Cl  (NH4)2 [PtCl6]  yellow + 2HCl
USES: (i) Used as a refrigeration fluid. (ii) For the production of ammonium fertilizers such as ammonium sulphate, ammonium
phosphate, ammonium nitrate, urea etc. (iii) For removing grease because NH4OH dissolves grease. (iv) For manufacture of
HNO3 by the Ostwald process. (v) As a laboratory reagent. (vi) In the production of artificial rayon, silk, nylon etc.
(2) OXIDES OF NITROGEN :
Nitrogen forms a number of oxides, N2O, NO, N2O3, NO2 or N2O4 and N2O5, and also very unstable NO3 and N2O6. All
these oxides of nitrogen exhibit p-p multiple bonding between nitrogen and oxygen.
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Name Formula Colour Remarks

Nitrous oxide N2O Colourless (g) Neutral ,+ 1 oxidation state

Nitric oxide NO Colourless (g) Neutral ,+ 2 oxidation state
Dinitrogen trioxide N2O3 Dark blue (s) Acidic ,+ 3 oxidation state
Nitrogen dioxide NO2 Brown (g) Acidic , + 4 oxidation state
Dinitrogen tetroxide N2O4 Colourless (s) Extensively dissociated to NO2 as

gas and partly dissociated as liquid,

acidic, + 4 oxidation state
Dinitrogen pentoxide N2O5 Colourless (s) Unstable as gas; ionic solid NO+2,
NO3– , acidic, +5 oxidation state

PREPARATION :
(i) N2O is obtained generally by heating NH4NO3 with caution.
NH4NO3  N2O + 2H2O ; 2NO + H2SO3  N2O + H2SO4
(ii) NO is best prepared by the reduction of 8 M HNO3 with reducing agents like Cu or by reduction of nitrous acid or nitrites by
Fe2+ or – ions.
3Cu + 8HNO3  3Cu(NO3)2 + 2NO + 4H2O
2NaNO2 + 2FeSO4 + 3H2SO4  2NaHSO4 + Fe2(SO4)3 + 2NO + 2H2O
2NaNO2 + 2NaI + 4H2SO4  4NaHSO4 + 2NO + I2 + 2H2O
(iii) N2O3 is obtained as an intense blue liquid or a pale blue solid on cooling an equimolar mixture of NO and NO2 to 250 K.
NO + NO2  N2O3
On warming, its colour fades due to its dissociation into these two oxides.
(iv) NO2 can be prepared by reduction of concentrated HNO3 with Cu or by heating heavy metal nitrates.
2Pb(NO3)2  2PbO + 4NO2 + O2
673 K
Cu + 4HNO3  Cu(NO3)2 + 2NO2 + 2H2O ;
(v) N2O5 is an anhydride of HNO3. It is best prepared by dehydrating HNO3 by P4O10 at low temperatures.
4HNO3 + P4O10   2N2O5 + 4HPO3
250K

PROPERTIES:
Oxides of nitrogen are all oxidizing agents, N2O even supporting the combustion of S and P. NO which is thermally more
stable, supports the combustion of Mg and P but not of S. Sulphur flame is not hot enough to decompose it.
N2O is isoelectronic with CO2 and also has a linear structure. However, unlike CO2, N2O has a small dipole moment.
NO has a total of 15 electrons. It is impossible for all of them to be paired and hence this is an odd electron molecule. In the
gaseous state, it is paramagnetic. However, the liquid and the solid states are diamagnetic because loose dimmers are formed
canceling out the magnetic effects of unpaired electrons.
The brown ring formed in the test for nitrates is due to the formation of a complex of iron, [Fe(H2O)5NO]2+.
NO2 with 23 electrons is again an odd electron molecule. In the gaseous state it is paramagnetic. On cooling, the gas
condenses to a brown liquid and eventually to a colourless solid both of which are diamagnetic due to dimerisation.
Liquid N2O4 undergoes self-ionization to form NO+ and NO3- ions and therefore, it has been extensively studied as a non-
aqueous solvent.

 N2O : (a) Reduction : Cu(hot) + N2O  CuO + N2

(b) Oxidation : 2KMnO4 + 3H2SO4 + 5N2O  K2SO4 + 2MnSO4 + 3H2O + 10NO
(c) Supporter of combustion : Mg + N2O  MgO + N2
 NO : (a) Supporter of combustion : S + 2NO  SO2 + N2
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(b) Oxidising properties (Reduction of NO) :

5H2 + 2NO  Pt  black
  2NH3 + 2H2O
SO2 + H2O + 2NO  H2SO4 + N2O
H2S + 2NO  H2O + N2O + S
(c) Reducing properties (oxidation of NO) :
2NO + X2  2NOX
6KMnO4 + 9H2SO4 + 10NO  3K2SO4 + 6MnSO4 + 4H2O + 10HNO3
 N2O3 : (a) N2O3 + KOH  2KNO2 + H2O
(b) It is anhydride of HNO2 :
2HNO2  N2O3 + H2O
(c) with concentrated acids, form nitrosyl salts
N2O3 + 2HClO4  2NO[CIO4] + H2O
 NO2 : It behaves both like HNO 2 and HNO3. It behaves like HNO 2 as a reducing agent and like HNO 3 as an
oxidising agent according to following reactions respectively.
2KMnO4 + 3H2SO4 + 10NO2 + 2H2O  K2SO4 + 2MnSO4 + 10HNO3
SO2 + H2O + NO2  H2SO4 + NO
* N2O4 is mixed anhydride of HNO3 and HNO2
 N2O5 : (a) 2N2O5  2N2O4 + O2
(b) N2O5 + 2NaOH  2NaNO3 + H2O
(c) N2O5 + I2  10 NO2 + I2O5
(3) Oxyacids of nitrogen :
(A) NITROUS ACID (HNO2) :
PREPARATION:
(i) By acidifying an aqueous solution of a nitrite
Ba(NO3)2 + H2SO4  2HNO2 + BaSO4
(ii) By passing an equimolar mixture of NO and NO2 into water:
NO + NO2 + H2O  2HNO2

PROPERTIES :
(i) It is an unstable, weak acid which is known only in aqueous solution.
(ii) On trying to concentrate, the acid decomposes as given below.
3HNO2  HNO3 + 2NO + H2O
(iii) Nitrous acid and nitrites are good oxidizing agents and convert iodides to iodine, ferrous salts to ferric, stannous to stannic
and sulphites to sulphates eg.
2KI + 2HNO2 + 2HCl  2H2O + 2NO + 2KCl + I2
(iv) With strong oxidizing agents like KMnO4 nitrous acid and nitrites function as reducing agents and get oxidized to NO3- ions:
2KMnO4 + 5KNO2 + 6HCl  2MnCl2 + 5KNO3 + 3H2O + 2KCl
(iii) Nitrite ion is a good coordinating agent. Both nitrogen and oxygen have lone pairs capable of forming coordinate bond with
metal ions. Nitrite ion can coordinate either through N or through O.(It is an ambidentate ligand) This generates linkage
isomerism. Analogous organic derivatives are also known, the nitrites, RONO and the nitro compounds RNO2 where R is
any alkyl or aryl group.

(B) NITRIC ACID (HNO3) :

PREPARATION :
(i) Laboratory method :
NaNO3 + H2SO4  NaHSO4 + HNO3
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(ii) HNO3 is now almost exclusively manufactured by the Ostwald process. In this process NH3 is catalytically oxidized to
NO over a Pt-Rh catalyst at 1200K.
4NH3 + 5O2  4NO + 6H2O H = -904 kJ
About 96 to 98 % of NH3 is converted into NO. The mixture is then diluted with air. NO combines with O2 to give NO2 which
is absorbed in water to give HNO3 and NO, which is then recycled.
2NO + O2  2NO2 ; 3NO2 + H2O  2HNO3 + NO
Nitric acid can be concentrated to 68 % by distillation, when a constant boiling mixture is formed. More concentrated acid
can be made by distilling the mixture with concentrated sulphuric acid.
PROPERTIES :
(i) Pure nitric acid is colourless liquil (bp 359oC). It decomposes readily in light giving a yellow colour due to the formation of
nitrogen dioxide. It is a strong acid and is almost completely dissociated into ions in solution.
(ii) Thermal stability

4HNO3  2H2O + 4NO2 + O2
(iii) Oxidising properties
2HNO3 (conc.)  H2O + 2NO2 + [O] ; 2HNO3 (dilute)  H2O + 2NO + 3[O]
(a) Oxidises H2S to sulphur
H2S + 2HNO3 (conc.)  2H2O + 2NO2 + S  ; 3H2S + 2HNO3 (dilute)  4H2O + 2NO + 3S

(b) Oxidises SO2 to H2SO4

SO2 + 2HNO3 (conc.)  H2SO4 + 2NO2  ; 3SO2 + 2H2O + 2HNO3 (dilute)  3H2SO4 + 2NO
 Similarly oxidises ferrous salts to ferric salts, halogen acids to respective halogens.
(iv) Reaction with non-metals.
C + 4HNO3  H2CO3 + H2O + 4NO2 ; S + 6HNO3  H2SO4 + 2H2O + 6NO2
2 + 10HNO3  2HO3 + 4H2O + 10NO2 ; P + 5HNO3  H3PO4 + H2O + 5NO2
 These reactions are given with conc. HNO3 .
(v) Reaction with metals :
(A) Metals that are more electropositive than hydrogen
(a) Action on zinc or Fe :
Zn + 4HNO3 (conc.)  Zn(NO3)2 + 2H2O + 2NO2 ; 4Zn + 10HNO3 (dil.)  4Zn(NO3)2 + 5H2O + N2O
4Zn + 10HNO3 (v.dil.)  4Zn(NO3)2 + NH4NO3 + 3H2O
 4Mg + 10HNO3 (v.dil.)  4Mg(NO3)2 + NH4NO3 + 3H2O
(b) Action on tin :
Sn + 4HNO3 (conc.)  H2SnO3 + 4NO2 + H2O ; 4Sn + 10HNO3 (dil.)  4Sn(NO3)2 + NH4NO3 + 3H2O
(c) Action on lead :
Pb + 4HNO3 (conc.)  Pb(NO3)2 + 2NO2 + 2H2O ; 3Pb + 8HNO3 (dil.)  3Pb(NO3)2 + 2NO + 4H2O
(B) Metals which are less electropositive than hydrogen.
(i) Action on copper
Cu + 4HNO3 (conc.)  Cu(NO3)2 + 2NO2 + 2H2O
3Cu + 8HNO3 (v.dil)  3Cu(NO3)2 + NO + 4H2O
(C) Metalloids : Sb and As.
Sb + 5 HNO3 (conc.)  H3SbO4 (antimonic acid) + 5 NO2 + H2O
 Mg & Mn only metals which produce hydrogen gas with cold (1 – 2%) HNO3.
Mg + 2HNO3  Mg(NO3)2 + H2Mn + 2HNO3  Mn(NO3)2 + H2
 p-BLOCK ELEMENTS

 As concentrated nitric acid (80%) behaves as an oxidizing agent and metals such as Al, Fe, Cr etc are rendered passive due
to the formation of a tenacious layer of insoluble oxide on the metal surface.
 Noble metals such as Au, Pt, Rh, and Ir are not attacked by nitric acid. However a 1:3 mixture of conc.
HNO3 and conc. HCl known as aqua regia dissolves Au and Pt as it contains free(atomic) chlorine:
HNO3 + 3HCl  2H2O + 2Cl + NOCl ; Au + 3Cl + HCl  HAuCl4 ; Pt + 4Cl + 2HCl  H2PtCl6
Brown ring test :
2HNO3 + 3H2SO4 + 6FeSO4  3Fe2(SO4)3 + 2NO + 4H2O
FeSO4 + NO + 5H2O  [Fe(H2O)5 NO]SO4

2. PHOSPHORUS :

It is a very reactive non-metal. It catches fire in air. It occurs in nature in the form of stable phosphates. (Animal bones also
contain calcium phosphate (58 %)). The important minerals are:
(i) Phosphorite, Ca3(PO4)2 (ii) Chloraptite, Ca3(PO4)2CaCl2
(iii) Fluoraptite, Ca3(PO4)2CaF2 (iv) Vivianite, Fe3(PO4)2·8H2O (v) Redonda phosphate, AlPO4
ALLOTROPIC FORMS OF PHOSPHORUS:
(i) White or yellow phosphorus (P4):
PREPARATION:

2Ca3(PO4)2 (From bone-ash) + 10C + 6SiO2  6CaSiO3 + 10CO + P4(s)
PROPERTIES:
It is white-to-transparent and soft waxy solid. Its density is 1.8 g/cc at 20oC. Its mp and bp are 44oC and 287oC respectively.
It is soluble in CS2 but insoluble in water. It glows in dark due to slow oxidation producing yellowish-green light. This
phenomenon is called phosphorescence
P4 + 5O2  P4O10
White phosphorus is poisonous. It turns yellow after some time; it is called yellow phosphorus. It undergoes oxidation in the
presence of air which slowly raises its temperature and due to its low ignition temperature (~ 30ºC) after a few moments it
catches fire spontaneously. Due to this reason, it is strored under water.
P 2.21Å
60
ºC
P P

P
* As readily oxidised, acts as a reducing agent.
P4 + 20HNO3  4H3PO4 + 20NO2 + 4H2O ; 3CaO + 8P + 9H2O  3Ca(H2PO2)2 + 2PH3
P4 + 3CuSO4 + 6H2O  Cu3P2 + 2H3PO3 + 3H2SO4
Cu3P2 + 5CuSO4 + 8H2O  8Cu + 5H2SO4 + 2H3PO4

Colloidal solution of gold may be prepared by reducing a solution of gold chloride with phosphours dissolved in ether.
(ii) Red phosphorus:
PREPARATION :
When white phosphorus is heated in the atmosphere of CO2 or coal gas at 573 K red phosphorus is prodouced. This red
phosphorus may still contain some white phosphours which is removed by boiling the mixture with NaOH where white
phosphorus is converted into PH3 gas but red phosphorus remains inert.
P4 + 3NaOH + 3H2O  PH3(g) + 3NaH2PO2
 It is also prepared by heating white phosphorus with a few crystals of iodine catalyst at 250oC under high pressure in
absence of air.
PROPERTIES :
It is a red crystalline solid having a density of 2.2 g/cc. It is less reactive than white phosphorus and does not dissolve in
liquid CS2. It does not catch fire at room temperature because its ignition temperature is 260oC.
 p-BLOCK ELEMENTS

It is a polymeric substance forming linear chains like this.

(iii) Black phosphorus:

It has two forms -black phosphorus and -black phosphorous

(a) -black phosphorous

P(red) tube
   P(-black)
insulated
803 K

-black phosphorous structure is not definite and is non conductor of electricity.

(b) -black phosphorous
 
473 K
P(white) High  P(-black)
pressure

-black phosphorous is an electrical conductor resembling graphite in this respect and also in its flakiness and
luster. It is insoluble in CS2. It has a layered structure like graphite.

P P P
P P P P

P P P P
P P P

P P P
P P
(iv) Brown phosphorus:
Above 1600oC, P4 molecules begin to dissociate into P2 molecules. Rapid cooling of this vapour gives brown phosphorus
which probably contains P2 molecules.
CHEMICAL PROPERTIES OF PHOSPHORUS :
 Reactivity of the various allotropic forms of phosphorus towards other substances decreases in the order:
Brown > white > red > black, the last one being almost inert.
Apart from their reactivity difference, all the forms are chemically similar.
(i) Action of air :
White phosphorus burns in air to form phosphorus trioxide and pentoxide.
P4 + 5O2  2P2O5 ; P4 + 3O2  2P2O3
Red and other forms of phosphorus also burn in air or oxygen but on heating.
(ii) Action of non-metals:
When heated with non-metals phosphorus forms compounds PX3, PX5, P2S3 and P2S5.
2P + 3X2  2PX3, 2P + 5X2  2PX5 (where X = Cl, Br, and I.)
(iii) Action with metals:
Alkali metals when heated with white phosphorus in vacuum produce alkali metal phosphide, which react with water to form
phosphine gas.

3M + P  M3P M3P + 3H2O   3MOH + PH3 { where M = Na, K etc.}
(iv) Action of NaOH:
When white phosphorus is heated with NaOH solution, phosphine gas is evolved.

P4 + 3NaOH + 3H2O  3NaH2PO2 + PH3

(v) Action of conc. HNO3 :
When heated with conc. HNO3, phosphorus is oxidized to H3PO4.

P + 5NHO3  H3PO4 + 5NO2 + H2O

 p-BLOCK ELEMENTS

(vi) Action of conc. H2SO4:

When heated with conc. H2SO4 phosphorus is oxidized to H3PO4.

2P + 5H2SO4  2H3PO4 + 5SO2 + 2H2O
 Conversion of white phosphorus to red phosphorus and red phosphorus to white phosphorus.
Heat in presence of 2 catalyst at 250oC and high pressure in absence of air
White phosphorus Red phosphorus
o
Heat above 250 C in presence of inert gas and condense in water

COMPOUNDS OF PHOSPHORUS :
(1) PHOSPHINE :
PREPARATION:
(i) By heating white phosphorus with NaOH solution in presence of coal gas. Phosphine gas is collected by the downward
displacement of water.

4P + 3NaOH + 3H2O  3NaH2PO2 + PH3
 Coal gas is used to prevent oxidation of phosphine. The phsophine gas is contaminated with a combustible gas P2H4. It is
separated from PH3 by passing the gaseous mixture through a freezing mixture whereupon P2H4 condenses to a liquid and
PH3 is collected by the downward displacement of air. Pure PH3 does not burn in air.
(ii) By the action of alkalies on phosphonium salts:

PH4I + NaOH  NaI + PH3 + H2O
(iii) By the action of dil. HCl or dil. H2SO4 on metal phosphides.

Na3P + 3HCl  3NaCl + PH3 AlP + 3HCl  AlCl3 + PH3

2Na3P + 3H2SO4  3Na2SO4 + 2PH3

(iv) H3PO2 + 4H   PH3 + 2H2O
Zn / HCl

PROPERTIES :
(i) It is a colourless gas with a smell of rotten fish and is neutral to litmus paper, It is heavier than air and only slightly soluble
in water, It is a poisonous gas and acts as a Lewis base.

(ii) Action of chlorine:

It reacts with Cl2 to form PCl5.

PH3 + 4Cl2  PCl5 + 3HCl

 Similar reaction occurs between heated phosphine and Br2 and I2 vapours.
(iii) Reaction with hydrogen halides: When PH3 is bubbled in solution of HX, phosphonium halides are formed.

PH3 + HX  PH4X

(iv) Action on CuSO4 solution:
When PH3 is bubbled in acidic solution of copper sulphate, a black precipitate of copper phosphide is formed.

3CuSO4 + 2PH3  Cu3P2 {black} + 3H2SO4

(v) Reaction with AgNO3 solution:
When PH3 gas is bubbled in a solution of AgNO3, a yellow precipitate of silver phosphide, Ag3P, is first formed which later
decomposes to black Ag.

3AgNO3 + PH3  Ag3P (yellow) + 3HNO3

Ag3P + 3AgNO3 + 3H2O  6Ag (black) + 3HNO3 + H3PO3
 p-BLOCK ELEMENTS

(vi) Reaction with mercuric chloride solution:

When mercuric chloride solution is treated with PH3 gas, a brownish black precipitate of mercuric phosphide is formed.

3HgCl2 + 2PH3  Hg3P2(brownish-black) + 6HCl

* Samples of PH3 can be dried using quick lime, or NaOH sticks. It cannot be dried by conc. H2SO4 because of its reaction with
it.

USES :
It is used in making smoke signals and producing smoke screens in battle-fields.

2. OXIDES OF PHOSPHORUS :
(A) PHOSPHORUS TRIOXIDE (P2O3) :
PREPARATION :
It is prepared by burning phosphorus in a limited supply of oxygen when gaseous P4O10 and P4O6 are formed. On lowering
the temperature using a condenser, P4O6 remains in gaseous form whereas P4O10 condenses as a solid which is stopped by
glasswool. On passing the remaining gaseous mixture through freezing mixture, it converts into colourless crystals of P4O6.

PROPERTIES :
(i) It is colourless crystalline solid having mp 23.8oC and bp 178oC.
(ii) It dissolves in cold water to form phosphorus acid. It is thus the anhydride of phosphorus acid.
P2O3 + 3H2O  2H3PO3

(iii) It dissolves in hot water liberating PH3

2P2O3 + 6H2O  3H3PO4 + PH3
(iv) It slowly gets oxidized in air to form P2O5
P2O3 + O2  P2O5
(v) It burns in Cl2 gas forming phosphorus oxytrichloride (POCl3) and phosphoryl chloride (PO2Cl)
P2O3 + 2Cl2  POCl3 + PO2Cl

(B) PHOSPHORUS PENTOXIDE (P2O5) :

PREPARATION :
It is obtained by burning phosphorus in air.
P4 + 5O2  P4O10
PROPERTIES:
(i) It is a white powder acidic in nature and is the anhydride of orthophosphoric acid. Its empirical formula is P2O5 and its
molecular formula is P4O10.
(ii) It sublimes on heating at 250oC.
(iii) Action of water:
It dissolves in water with hissing sound forming metaphosphoric acid and finally orthophosphoric acid.

P4O10 + 2H2O  4HPO3 ; HPO3 + H2O  H3PO4

(iv) Dehydrating power:
It dehydrates conc. H2SO4 and conc. HNO3 to SO3 and N2O5 respectively.
2HNO3 + P2O5    2HPO3 + N2O5 ; H2SO4 + P2O5 
distillati on
  2HPO3 + SO3
distillati on

USES :
(i) For drying acidic gases (ii) As a dehydrating agent
(iii) For the preparation of SO3 and N2O5 (iv) For the preparation of phosphoric acid
 p-BLOCK ELEMENTS

3. OXY-ACIDS OF PHOSPHORUS :
(A) PHOSPHORUS ACID (H3PO3) :
PREPARATION:
(i) By dissolving P2O3 in water:

P2O3 + 3H2O  2H3PO3

(ii) By hydrolysis of PCl3 with water:

PCl3 + 3H2O  H3PO3 + 3HCl

The solution containing H3PO3 and HCl is heated to 180oC and HCl gas is driven out. The resulting solution on crystallization
gives white crystals of H3PO3.
(iii) By heating hypophosphorus acid :
40or more
3H3PO2 (concentrated solution)    PH3 + 2H3PO3
PROPERTIES:
(i) It is a white crystalline solid, soluble in water and having melting point of 74oC.
(ii) It is a weak acid and a reducing agent
(iii) When neutralized with bases or alkalies, it forms neutral salts called phosphites which are unstable.

H3PO3 + 3NaOH  Na3PO3 + 3H2O

Its basicity is 2 because it has only two replaceable H atoms. The third H atom is not replaceable because it is not connected
to oxygen.
(iv) 
4H3PO3  3H3PO4 + PH3 (Disproportionation)

(v) H3PO3 + 3PCl5  PCl3 + 3POCl3 + 3HCl

(vi) It is a strong reducing agent :

2AgNO3 + H3PO3 + H2O  2Ag + 2HNO3 + H3PO4

2HgCl2 + H3PO3 + H2O  Hg2Cl2 + 2HCl + H3PO4

(B) ORTHOPHOSPHORIC ACID (H3PO4) :

PREPARATION:

(i) By heating calcium phosphate with conc. H2SO4

Ca3(PO4)2 + 3H2SO4  2CaSO4 + 2H3PO4

CaSO4 is insoluble. Solution of H3PO4 is separated from CaSO4. It is then concentrated by evaporating it at 180oC and
dehydrated by conc. H2SO4 placed in a vacuum dessicator cooled by freezing mixture. White crystals of H3PO4 are thus
formed.
(ii) By hydrolysis of PCl5:

PCl5 + 4H2O  H3PO4 + 5HCl

(iii) By heating white phosphorus with conc. HNO3:

P + 5HNO3  H3PO4 + 5NO2 + H2O

PROPERTIES :
(i) Pure orthophosphoric acid is a white crystalline solid highly soluble in water having melting point of 42oC. It is a weak acid.
It forms two acid salts and one normal salt.NaH2PO4 is sodium dihydrogen phosphate,Na2HPO4 is disodium hydrogen
phosphate & Na3PO4 is sodium orthophosphate.
(ii) Action of heat :
H3PO4    H4P2O7 (pyrophosphoric acid) ;
220 º C H4P2O7    HPO3 (metaphosphoric acid)
316 º C
 p-BLOCK ELEMENTS

(iii) Neutralization with alkalies or bases:

H3PO4  NaH PO (pri. phosphate)  NaHPO (sec. phosphate)   Na PO (tert. phosphate)
NaOH NaOH NaOH
H2O 2 4 H2O 4 H2O 3 4

 
NaH2PO4  NaPO3 + H2O

USES:
It is used as a laboratory reagent and in manufacture of medicines.

GROUP SIXTEEN ELEMENTS : THE OXYGEN FAMILY

Oxygen, sulphur, selenium, tellurium and polonium constitute group 16 of the periodic table. This is sometimes known as
group of chalcogens. The name is derived from the greek word for brass and points to the association of sulphur and its
congeners with copper. Most copper minerals contain either oxygen or sulphur and frequently the other members of the
group.
Occurrence :
Oxygen is the most abundant of all the elements on the earth. Oxygen forms about 46.6% by mass of earth’s crust . Dry air
contains 20.946% oxygen by volume.
However, the abundance of sulphur in the earth’s crust is only 0.03-0.1%. Combined sulphur exists primarily as sulphates
such as gypsum CaSO4.2H2O, epsom salt MgSO4 .7H2O, baryta BaSO4 and sulphides such as galena PbS, zinc blende ZnS,
copper pyrites CuFeS2 . Traces of sulphur occur as hydrogen sulphide in volcanoes.
Selenium and tellurium are also found as metal selenides and tellurides in sulphide ores. Polonium occurs in nature as a
decay product of thorium and uranium minerals.
Electronic Configuration :
The elements of group 16 have six electrons in the outermost shell and have ns2 np4 general electronic configuration.
Atomic and Ionic Radii :
Due to increase in the number of shells , atomic and ionic radii increase from top to bottom in the group. The size of oxygen
atoms is however, exceptionally small .
Ionisation Enthalpy :
Ionisation enthalpy decrease down the group. It is due to increase in size. However, the element of this group have lower
ionisation enthalpy values compared to those of group 15 in the corresponding periods. This is due to the fact that group 15
element have extra stable half-filled p orbitals elelctronic configurations.
Electron Gain Enthalpy :
Because of the compact nature of oxygen atom, it has less negative electron gain enthalpy than sulphur. However from
sulphur onwards the value again becomes less negative upto polonium.
Electronegativity :
Next to fluorine, oxygen has the highest electronegativity value amongst the elements. Within the group, electronegativity
decrease with an increase in atomic number. This implies that the metallic character increase from oxygen to polonium.
Physical Properties :
Oxygen and sulphur are non-metal, selenium and tellurium metalloids, whereas polonium is a metal. Polonium is radioactive
and is short lived (Half-life 13.8 days). All these element exhibit allotropy. The melting and boiling points increase with an
increase in atomic number down the group. The larger difference between the melting and boiling points of oxygen and
sulphur may be explained on the basis of their atomicity; oxygen exist as diatomic molecules (O2) whereas sulphur exists as
polyatomic molecule (S8).
 p-BLOCK ELEMENTS

ATOMIC & PHYSICAL PROPERTIES :

Element O S Se Te
Atomic Number 8 16 34 52
Atomic Mass 16 32.06 78.96 127.6
2 4 2 4 10 2 4
Electronic configuration [He] 2s 2p [Ne] 3s 3p [Ar] 3d 4s 4p [Kr] 4d105s2 5p4
Covalent Radius / pm 74 103 119 142
–2
Ionic Radius X / pm 140 184 198 221
 1314 1000 941 869
Ionization enthalpy / (kJ mol–1)
 3388 2251 2045 1790
Electronegativity 3.5 2.44 2.48 2.01
–3
Density/[g cm (293 K)] 1.32 2.06 4.19 6.25
Melting point / K 54 393 490 725
Boiling point / K 90 718 958 1260

Chemical Properties :
Oxidation states and trends in chemical reactivity :
The elements of group 16 exhibit a number of oxidation states. The stability of -2 oxidation state decreases down the group.
Polonium hardly shows -2 oxidation states. Since electronegativity of oxygen is very high, it shows only negative oxidation
states as -2 except in the case of OF2 where its oxidation states is + 2. Other elements of the group exhibit + 2 + 4 + 6
oxidation states but + 4 and + 6 are more common. Sulphur, selenium and tellurium usually show + 4 oxidation in their
compounds with oxygen and +6 oxidations state with fluorine. The stability of +6 oxidation state decreases down the group
and stability of + 4 oxidation state increases (inert pair effect). Bonding in + 4 and + 6 oxidation states are primarily covalent.
Anomalous behaviour of oxygen :
The anomalous behaviour of oxygen, like other member of p-block present in second period is due to its small size and high
electronegativity. One typical example of effects of small size and high electronegativity is the presence of strong hydrogen
bonding in H2O which is not found in H2S.
The absence of d orbitals in oxygen limits its covalency to four and in practice, rarely exceeds two. On the other hand, in case
of other elements of the group, the valence shell can be expanded and covalence exceeds four.
(i) Reactivity with hydrogen : All the elements of group 16 form hydrides of the type H2E (E = S, Se., Te, Po). Some properties
of hydrides are given in Table. Their acidic character increases from H2O to H2Te. The increase in acidic character can be
explained in terms of decrease in bond (H-E) dissociation enthalpy down the group. Owing to the decrease in bond (H-E)
dissociation enthalpy down the group, the thermal stability of hydrides also decreases from H2O to H2Po. All the hydrides
except water possess reducing property and this character increases from H2S to H2Te.
Table : Properties of Hydrides of Group 16 Elements
Property H2 O H2 S H2Se H2Te
m.p./K 273 188 208 222

b.p./K 373 213 232 269

H-E distance/pm 96 134 146 169

HEH angle (º) 104 92 91 90

fH/kJ mol-1 -286 -20 73 100

diss H (H-E)/kJ mol-1 463 347 276 238

Dissociation constanta 1.8 × 10-16 1.3 × 10-7 1.3 × 10-4 2.3 × 10-3
 p-BLOCK ELEMENTS

(ii) Reactivity with oxygen : All these elements form oxides of the EO2 and EO3 types where E = S, Se, Te or Po. Ozone (O3)
and sulphur dioxide (SO2) are gases while selenium dioxide (SeO2) is solid. Reducing property of dioxide decreases from
SO2 to TeO2 ; SO2 is reducing while TeO2 is an oxidising agent. Besides EO2 type sulphur, selenium and tellurium also form
EO3 type oxide (SO3, SeO3, TeO3). Both types of oxides are acidic in nature.
(iii) Reactivity toward the halogens : Elements of group 16 form a larger number of halides of the type
EX6, EX4 and EX2 where E is an element of the group and X is an halogen. The stabilities of the halides decrease in the
order F > Cl > Br > l. Amongst hexahalides, hexafluorides are the only stable halides. All hexafluorides are gaseous in
nature. They have octahedral structure. Shulphur hexafluoride SF\6 is exceptionally stable for steric reasons.
Amongst terrafluorides, SF4 is a gas , SeF4 liquid and TeF4 a solid These fluorides have sp3d hybridisation and thus, have
trigonal bipyramidal structure in which one of the equatorial position is occupied by a lone pair of electrons. This geometry
is also regarded as see - saw geometry.
All elements except selenium form dichlorides and dibromides. These dihalides are formed by sp3 hybridisation and thus
have tetrahedral structure. The well known monohalides are dimeric in nature, Examples are
S2F2, S2Cl2, S2Br2, Se2Cl2 and Se2Br2. These dimeric halides undergo disproportionation as given below :
2Se2Cl2  SeCl4 + 3Se.
1. DIOXYGEN (O2) :
It differs from the remaining elements of the VIth group because of the following properties.
(A) small size (B) high electronegativity and (C) non-availability of d-orbitals.
PREPARATION :
(i) By thermal decomposition of oxides of metals.
0 0
2 HgO   2 Hg + O2 ;
450 C 2 Ag2O   4 Ag + O2
350 C

3 MnO2  Mn3O4 + O2 ; 

2 Pb3O4  6 PbO + O2
(ii) By thermal decomposition of oxygen rich compounds.

2 NaNO3  
2NaNO2 + O2 ; 2 KClO3  2 KCl + 3O2 (laboratory method)
4 K2Cr2O7   
4 K2CrO4 + 2 Cr2O3 + 3O2 ; 2 KMnO4  K2MnO4 + MnO2 + O2
(iii) By the action of conc. H2SO4 on MnO2.

2 MnO2 + 2H2SO4  2 MnSO4 + 2H2O + O2

(iv) By the action of water on Na2O2.

2 Na2O2 + 2 H2O  4 NaOH + O2

(v) By the action of conc. H2SO4 on KMnO4 or K2Cr2O7.

4 KMnO4 + 6 H2SO4  2 K2SO4 + 4MnSO4 + 6H2O + 5O2

2 K2Cr2O7 + 8H2SO4  2 K2SO4 + 2Cr2(SO4)3 + 8H2O + 3O2
(vi) By Brins process (mfg.) :
0 0
2 BaO + O2(air)   2BaO2 ; 2 BaO2 
500 C
 2 BaO + O2
800 C

(vii) From air (mfg.) :

Oxygen is obtained by liquification of air and then its fractional distillation.
PROPERTIES:
16 17
Colourless , odourless and tasteless gas. It is paramagnetic and exhibits allotropy. Three isotopes of oxygen are 8O , 8O
18
and 8O . Oxygen does not burn but is a strong supporter of combustion.
USE :
(i) Oxygen mixed with helium or CO2 is used for artificial respiration. (ii) Liquid oxygen is used as oxidising agent in rocket
fuels. (iii) Oxygen is used for production of oxy-hydrogen or oxy-acetylene flames employed for cutting and welding.
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2. OXIDES :

(i) Acidic oxides

They dissolve in water forming oxyacids , e.g., CO2, SO2 , SO3, N2O5 , N2O3 , P4O6 , P4O10, Cl2O7, CrO3 , Mn2O7 , V2O5.

Cl2O7 + H2O  2 HClO4 ; Mn2O7 + H2O  2 HMnO4

(ii) Basic oxides
They either dissolve in water to form alkalies or combine with acids to form salts and water or combine with acidic oxides to
form salts; e.g., Na2O, CaO. CuO, FeO, BaO etc.

Na2O + H2O  2 NaOH ; CaO + H2O  Ca(OH)2 ; CuO + H2SO4  CuSO4 + H2O
(iii) Neutral Oxides
They neither combine with acids nor with the bases to form salts e.g., CO, N2O, NO etc.
(iv) Amphoteric Oxides
These can combine with acids as well as bases e.g., ZnO, Al2O3, BeO, Sb2O3, Cr2O3, PbO etc.

PbO + 2 NaOH  Na2 PbO2 + H2O ; PbO + H2SO4  PbSO4 + H2O

Cr2O3 + 2 NaOH  Na2Cr2O4 + H2O; Cr2O3 + 3 H2SO4  Cr2(SO4)3 + 3 H2O
(v) Mixed Oxides
They behave as mixture of two simple oxides,
e.g., Pb3O4 (2PbO + PbO2), Fe3O4 (FeO + Fe2O3), Mn3O4 (2 MnO + MnO2)
(vi) Peroxides
They react with dilute acids and form H2O2, e.g., Na2O2, K2O2, BaO2 etc.
Na2O2 + H2SO4  Na2SO4 + H2O2
They react with water forming O2 .
Na2O2 + H2O  2NaOH + 1/2O2
(vii) Dioxides
Like peroxide, they contain excess of oxygen but do not yield H2O2 with dil. acids e.g. PbO2, MnO2 etc.
They evolve Cl2 with conc. HCl and O2 with conc. H2SO4.

MnO2 + 4HCl  MnCl2 + Cl2 + 2H2O; 2MnO2 + 2H2SO4  2MnSO4 + O2 + 2H2O
(viii) Super Oxides
They contain O2– ion, e.g., KO2 , RbO2 and CsO2 . These oxides react with water forming H2O2 and O2

2 KO2 + 2 H2O  2 KOH + H2O2 + O2.

(ix) Sub Oxides
They contain less oxygen than expected from the normal valency of the elements e.g., C3O2, N2O, Pb2O, Hg2O etc.

 C3O2  O  C  C  C  O
sp sp sp
2. OZONE (O3) :
PREPARATION:
It is prepared by passing silent electric discharge through pure and dry oxygen
O2   O + O
energy

O2 + O  O3 ; H = 2845 kJ mol-1

–––––––––––––––––––––––––––––––––
3O2 2O3
 Mixture obtained contains 5-10% ozone by volume and this mixture is called ozonised oxygen. The apparatus used for this
is called as ozoniser ((i) Simen’s and (ii) Brodie’s ozonisers).
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PROPERTIES :
(i) Pale blue gas which forms a blue liquid on cooling and on solidification forms violet black crystals. It has a strong fish-like
smell and is slightly soluble in water but more in turpentine oil, glacial acetic acid or CCl 4 .
O3 molecule is diamagnetic but O3– is paramagnetic.
(i) Oxidising agent :
O3 + 2H+ + 2 e  O2 + H2O ; SRP = + 2.07 v (In acidic medium)
O3 + H2O + 2e  O2 + 2OH– ; SRP = + 1.24 v (In alkaline medium)
Therefore, ozone is a strong oxidising agent in acidic medium.
(a) It oxidises – to I2 (from neutral solution of K)

O3  O2 + [O]

 Alkaline K is oxidised to potassium iodate & periodate.

K + 3O3  KO3 + 3O2 ; K + 4O3  KO4 + 4O2

Similarly S2–  SO42– (but not H2S), NO2–  NO3–, SO3–  SO42–, AsO33–  AsO43– , MnO42–  MnO4– , Sn2+
 Sn+4 & [Fe(CN)6]4–  [Fe(CN)6]3– in acidic medium.
(b) It oxidises moist S, P, As into their oxy acids.
O3  O2 + [O] × 3
S + 3 [O]  SO3

(c) It oxidises H2S to S

H2S + O3  H2O + S  (yellow)

(ii) Reaction with dry I2:

2 I2 + 9[O3]  I4O9 + 9O2

 I4O9 yellow solid has the composition I+3 (IO3–)3. Formation of this compound is a direct evidence in favour of basic nature
of I2 (i.e. its tendency to form cations).
(iii) Reaction with moist iodine :

O3  O2 + [O] × 5
I2 + 5[O]  I2O5

(iv) Reaction with Silver :

Silver articles become black in contact with ozone.
Ag + O3  Ag2O  (black) + O2
(v) Reaction with H2O2 :

2e– + 2H+ + O3  O2 + H2O

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It is supported by the fact that SRP of ozone is higher (+2.07) than SRP of hydrogen peroxide (+1.77). Therefore , ozone is
stronger oxidising agent than hydrogen peroxide.
(vi) Bleaching Action :
O3 also bleaches coloured substances through oxidation
(vii) Ozonolysis :
Alkenes, alkynes react with ozone forming ozonides.
O
CH2 CH2 Zn  H2O
CH2 = CH2 + O3    2HCHO
 ZnO
O O
(viii) Reaction with KOH :
Forms orange coloured compound, potassium ozonide.

2 KOH + 5O3  2 K O   5O  H O
3 2 2

(orange solid)
TESTS FOR OZONE

(i) A filter paper soaked in a alcoholic benzidine becomes brown when brought in contact with O3

(this is not shown by H2O2)

(ii) Tailing of mercury
Pure mercury is a mobile liquid but when brought in contact with O3 its mobility decreases and it starts sticking to glass
surface forming a type of tail due to the dissolution of Hg2O (mercury sub-oxide) in Hg.
2 Hg + O3  Hg2O + O2
USES :
(i) As a germicide and disinfectant for sterilising water and improving the atmosphere of crowded places.
(ii) For detecting the position of double bond in the unsaturated organic compounds.
(iii) In mfg. of artificial silk, synthetic camphor, KMnO4 etc.

3. HYDROGEN PEROXIDE (H2O2) :

PREPARATION :
(i) Laboratory method
BaO2 . 8H2O + H2SO4 (cold)  BaSO4  (white) + H2O2 + 8H2O
BaSO4 is filtered to get aqueous hydrogen peroxide.
 Ba(OH)2 + H2O2 + 6H2O  BaO2 . 8H2O
 BaO2 + 2HCl (ice cold)  BaCl2 + H2O2
Not possible to isolate H2O2 from this solution as BaCl2 is soluble in water
 The reaction between anhydrous BaO2 and H2SO4 is slow and practically ceases after sometimes due to the formation of a
protective layer of BaSO4 on BaO2.
 Since H2SO4 can decompose H2O2 at a higher temperature, therefore, the reaction should be carried out at low temperature
or H3PO4 can be used in place of H2SO4
3BaO2 + 2H3PO4  Ba3((PO4)2  + 3H2O2 ; Ba3(PO4)2 + 3H2SO4  3BaSO4  + 2H3PO4
H3PO4 can be used again.
(ii) By electrolysis of conc. H2SO4 at 00C using inert electrodes (platinum).
H2SO4 H +
1
at anode :   S2O82- + 2H+ + 2e ; at cathode :  H+ + e  H2
2
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80  90 0 C
H2S2O8 + H2O
distillation
2H2SO4   BaSO4  (white) + H2O2 (aq)
BaCl 2

BaSO4 is removed by filteration to get aqueous H2O2.

(iii) Industrial method (Auto oxidation):

OH O
C2H5 O2 (air) C2H5
(Oxidation) + H2O2
H2 (Ni)
(Reduction)
OH O
2- Ethyl anthraquinol 2-Ehtylanthraquinone
K2S2O8 (s) + 2D2O  2KDSO4(aq) + D2O2()

PROPERTIES :
(i) Colourless viscous liquid which appears blue in the larger quantity and is soluble in water (due to H- bonding) in all propor-
tions and form a hydrate H2O2.H2O (mp 221 K)
(ii) Its boiling point 1440C more than water but freezing point (-4) less than water. Density and dielectric constant are also
higher than H2O
(iii) Its aqueous solution is more stable than the anhydrous liquid where it decomposes into water and O2 slowly on exposure to
light.
2H2O2  2H2O + O2
H2O2 is not kept in glass containers because traces of alkali metal ions from the glass can catalyse the explosive decomposi-
tion of H2O2 Therefore, aqueous solution is stored in plastic or wax-lined glass containers and some urea or phosphoric acid
or glycerol is added to that solution because these compounds have been found to behave as negative catalyst for the
decomposition of H2O2
(iv) Acidic nature :
Behaves as a weak acid according to the following equation
H2O2 (aq) H+ + HO2- ; Ka = 1.5 × 10-12 at 250 C
Aqueous solution of H2O2 turns blue litmus red which is then bleached by the oxidising property of H2O2
Na2CO3 + H2O2  Na2O2 + H2O + CO2
Ba(OH)2 + H2O2 + 6H2O  BaO2 . 8H2O 

 A 30% H2O2 solution has pH = 4.0

(v) Oxidising Agent :
2 e + 2H+ + H O  2H O ; SRP = + 1.77 v
2 2 2
(In acidic medium)
2 e + H2O2  2OH ; SRP = + 0.87 v (In alkaline medium)
-

 On the basis of the above potentials, we can say that H2O2 is strong oxidising agent in acidic medium but kinetically it is
found that reactions are faster in basic medium.
(A) In acidic medium :
(a) It oxidises PbS to PbSO4.
H2O2  H2O + [O] × 4
PbS + 4[O]  PbSO4
––––––––––––––––––––––––––––
PbS + 4H2O2  PbSO4 + 4H2O
This property is utilised in restoring the white colours in old paintings which turns black due to the formation of PbS by the
action of atmospheric H2S.
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(b) H2O2 oxidises H2S to sulphur.

H2O2  H2O + [O]
H2S + [O]  H2O + S 
––––––––––––––––––––––––––
H2O2 + H2S  2H2O + S 
 H2O2 in acidic medium also oxidises AsO33-  AsO43- , SO32-  SO42- , KI  I2 , S2-  SO42-,
FeSO4  Fe2(SO4)3 & [Fe(CN)6]4-  [Fe(CN)6]3-
(c) NH2 - NH2 (hydrazine) + 2H2O2  N2 + 4H2O

(d) + H2O2  

FeSO 4 + H2O

(B) In alkaline medium :

(a) Cr(OH)3 (s) + 4 NaOH + 3H2O2  2Na2CrO4 (aq.) + 8H2O
or
10 OH + 3 H2O2 + 2 Cr3+  2 CrO42– + 8H2O
–

(b) 2NaBO2 + 2H2O2 + 6H2O  Na2 [(OH)2 B(O-O)2 B(OH)2 ] 6H2O (sodium per oxoborate)
 Used as a brightner in washing powder.
(vi) Reducing Agent :
It acts as a reducing agent towards powerful oxidising agnet.
H O  O + 2H+ + 2 e
2 2 2
 In alkaline solution, its reducing character is more than in acidic medium.
2 OH- + H2O2  O2 + 2H2O + 2 e
(a) Ag2O is reduced to Ag.
Ag2O + H2O2  2Ag + H2O + O2
(b) It reduces O3 to O2.
H2O2 + O3  H2O + 2O2

(c) It reduces ferric cyanide to ferrous cyanide (basic medium).

2 K3 [Fe(CN)6] + 2KOH  K4[Fe(CN)6] + H2O + O
H2O2 + O  H2O + O2
–––––––––––––––––––––––––––––––––––––––––––––––––
2K3[Fe(CN)6] + 2KOH + H2O2  2K4 [Fe(CN)6] + 2H2O + O2
 It also reduces MnO4-  Mn2+ (acidic medium), MnO4-  MnO2 (basic medium),
OCl–  Cl–, IO4–  IO3– & Cl2  Cl–

TESTS FOR H2O2 :

(i) With K2Cr2O7
K2Cr2O7 + H2SO4 + H2O2  K2SO4 + 2 CrO5 + 5 H2O
or
Cr2O72- + 2H+ + 4H2O2  2CrO5 + 5H2O
 CrO5 bright blue coloured compound soluble in ether.
CrO5 + H2SO4  2Cr2 (SO4)3 + 6H2O + 7O2

OH
(ii) 2 HCHO + H2O2 2 HCOOH + H2
pyrogallol
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When this reaction is carried out in dark, it is accompanied by emission of light (yellow coloured). It is an example of
chemiluminescene.
(iii) An acidified solution of titanium salt gives yellow or orange colour with H2O2.
Ti+4 + H2O2 + 2H2O  H2TiO4 (yellow/orange) + 4H+
USES :
(i) In bleaching of delicate materials such as silk, wool, cotton, ivory etc.
(ii) As a valuable antiseptic and germicide for washing wounds, teeth and ears under the name perhydrol.
(iii) As ‘antichlor’ to remove traces of chlorine and hypochlorite.
(iv) As oxidising agent in rocket fuels

4. SULPHUR (S) :
Sulphur Allotropic Froms :
Sulphur forms numerous allotropes of which the yellow rhombic ( - sulphur) and monoclinic ( - sulphur) forms are the
most important. The stable forms at room temperature is rhombic sulphur, which transfroms to monoclinic sulphur when
heated above 369 K.
Rhombic sulphur (- sulphur) :
This allotrope is yellow in colour , m.p. 385.8 K and specific gravity 2.06. Rhombic sulphur crystals are formed on evaporating
the solution of roll sulphur in CS2. It is insoluble in water but dissolved to some extent in benzene, alcohol and ether. It is
readily soluble in CS2 .

Monoclinic sulphur ( - sulphur) :

Its m.p. is 393 K and specific gravity 1.98. It is soluble in CS2. This form of sulphur is prepared by melting rhombic sulphur
in a dish and cooling till crust is formed. Two holes are made in the crust and the remaining liquid poured out. On removing
the crust, colourless needle shaped crystals of  - sulphur are formed. It is stable above 369 K and transforms into  - sulphur
below it . Conversely, - sulphur is stable below 369 K and transfroms into  - sulphur above this. At 369 K both the forms
are stable. This temperature is called transition temperature.
Both rhombic and monoclinic sulphur have S8 molecules these S8 molecules are packed to give different crystal structures.
The S8 ring in both the forms is puckered and has a crown shape. The molecular dimensions are given in figure.

S
20 S 205.7 pm
S
4 pm S S S
107o o
S S 102.2
S S S
S S (b)
(a)
S

Fig. : The structures of (a) S8 ring in rhombic sulphur and (b) S6 form
Several other modifications of sulphur containing 6-20 sulphur atoms per ring have been synthesised in the last two decades.
In cyclo- S6, the ring adopts the chair form and the moleculatr dimension are as shown in fig. (b) At elevated temperatures (~
1000 K ), S2 is the dominant species and is paramagnetic like O2.

3. COMPOUNDS OF SULPHUR :
(A) SODIUM THIOSULPHATE (Na2S2O3 .5H2O) :
PREPARATION :

(i) Na2SO3 + S Na2S2O3

(ii) Na2CO3 + 2SO2 (excess) + H2O  2NaHSO3 + CO2 ; 2NaHSO3 + Na2CO3  2Na2S2O3 + H2O + CO2
(iii) 2 NaHS + 4NaHSO3  3Na2S2O3 + 3H2O
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(iv) Na2S + Na2SO3 + I2  Na2S2O3 + 2 NaI

(V) 
2Na2S3 + 3O2 (from air)  2Na2S2O3 + 2S
PROPERTIES :
(i) It is a colourless crystalline substance soluble in water which loses water of crystallisation on strong heating
(ii) As antichlor :
It removes the chlorine from the surface of fibres (while dyeing) according to following reaction.
Na2S2O3 + Cl2 + H2O  Na2SO4 + 2HCl + S
Therefore , it is known as antichlor
(iii) Reaction with HCl :
Na2S2O3 + HCl  2NaCl + SO2 + S + H2O
This test is used for distinction between S2O32- and SO32- ions as SO32- ions give only SO2 with HCl.

(iv) Complex formation reactions :

(a) Reaction with silver salts (AgNO3 , AgCl, AgBr or AgI) :
Na2S2O3 + 2AgNO3  Ag2S2O3  (white) + 2 NaNO3
Ag2S2O3 + H2O  Ag2S  (Black) + H2SO4
If hypo is in excess, then soluble complex is formed.
2Na2S2O3 + AgNO3  Na3[Ag(S2O3)2] (soluble complex) + NaNO3
This reaction is utilized in photography where hypo is used as fixer.
(b) Reaction with FeCl3:
It develops a pink or violet colour which soon vanishes according to following reaction.
Fe3+ + 2S2O32–  [Fe(S2O3)2]– (Pink or violet)
[Fe(S2O3)2]– + Fe3+  2Fe2+ + S4O62–
(c) Reaction with AuCl3 (Soluble in water) :
AuCl3 + Na2S2O3  AuCl  + Na2S4O6 + 2HCl
AuCl + Na2S2O3  Na3 [Au(S2O3)2] (soluble complex) + NaCl
(d) Reaction with CuCl2 :
2 CuCl2 + 2Na2S2O3  2CuCl  + Na2S4O6 + 2 NaCl
CuCl + Na2S2O3  Cu2S2O3  + 2 NaCl
3 Cu2S2O3 + 2 Na2S2O3  Na4 [Cu6(S2O3)5] (soluble complex)
(e) Reaction with bismuth :
Bi3+ + 3 Na2S2O3  Na3[Bi(S2O3)3] (soluble complex) + 3Na+
But it soon decomposes to give black ppt. of Bi2S3
(v) Reaction with HgCl2 :
Na2S2O3 + HgCl2  Hg2S2O3 + 2NaCl
 +H2O
HgCl2 . 2HgS   HgS  (Black)

HgCl2

(vi) As reducing agent In iodometric titration :

(a) I2 + 2S2O32–  2I– + S4O62–
(b) 2 KMnO4 + Na2S2O3  K2SO4 + Na2SO4 + Mn2O3
215C 220C
(viI) 4Na2S2O3 .5H2O   4Na2S2O3   3Na2SO4 + Na2S5
H2O ( All)

USES :
(i) As an ‘antichlor’ to remove excess of chlorine from bleached fabrics.
(ii) In photography as fixer.
(iii) As a reagent in idometric and idiometric titrations.
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(B) HYDROGEN SULPHIDE (H2S) :

PREPARATION:
(i) FeS + H2SO4  FeSO4 + H2S
It is prepared in kipp’s apparatus
(ii) Preparation of pure H2S gas
Sb2S3 (pure) + 6 HCl (pure)  2 SbCl3 + 3 H2S

PROPERTIES :
(i) Colourless gas with rotten egg smell
(ii) Moderately soluble in water but solubility decreases with increasing temperature.
(iii) Reducing Agent :
Acts as a strong reducing agent as it decomposes evolving hydrogen.
(a) H2S + X2  2 HX + S;
(b) H2S + SO2   H2O + S;
moisture

(c) H2O2 + H2S  H2O + S + O2

(d) 2HNO3  H2O + 2NO2 + [O]
H2S + [O] H2O + S
2HNO3 + H2S 2H2O + NO2 + S

 It also reduces KMnO4  Mn2+, H2SO4  SO2 & K2Cr2O7  Cr3+

(iv) Acidic Nature :
Its aquesous solution acts as a weak dibasic acid according to following reaction
H2S HS + H+ S2- + 2H+
Therefore, It forms two series of salts as given below
NaOH + H2S  NaHS + H2O ; NaOH + H2S  Na2S + 2H2O
(v) Formation of Polysulphides :
They are obtained by passing H2S gas through metal hydroxides.
Ca(OH)2 + H2S  CaS + 2H2O ; CaS + 4 H2S  CaS5 + 4H2
NH4OH + H2S  (NH4)2S + 2H2O; (NH4)2S + H2S (excess)  (NH4)2 Sx+1 + xH2
yellow ammonium sulphide
TESTS FOR H2S :
(i) Turns acidified lead acetate paper black
(ii) Gives violet or purple colouration with sodium nitropruside solution.
USES :
(i) As a loboratory reagent for the detection of basic radicals in qualitative analysis.
(ii) As reducing agnet.

(C) SULPHUR DIOXIDE :

PREPARATION :
(i) S + O2 or air   SO2
Burn

(ii) S + 2H2SO4 (conc.)   3SO2 + 2H2O

(iii) By heating Cu or Ag with conc. H2SO4
Cu + H2SO4  CuSO4 + 2H2O + SO2
(iv) By reaction of metal sulphites with dil.HCl
Na2SO3 + 2HCl  2NaCl + SO2 + H2O
Similarly bisulphites also give SO2 with dil. HCl
NaHSO3 + HCl  NaCl + SO2 + H2O
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(v) By heating sulphides in excess of air

2 ZnS + 3O2  2ZnO + 2SO2

(vi) CaSO4 (gypsum) + C 2 CaO + SO2 + CO2

 By this method SO2 is obtained in large scale

PROPERTIES :
(i) Colourless gas with burning sulphur smell.
(ii) It is heavier than air and is highly soluble in water\
(iii) Neither burns nor helps in burning but burning magnesium and potassium continue to burn in its atmosphere.
3Mg + SO2  2 MgO + MgS ; 4K + 3SO2  K2SO3 + K2S2O3
(iv) Acidic Nature :
Acidic oxide and thus dissolve in water forming sulphurous acid.
SO2 + H2O  H2SO3
(v) Addition Reaction :
SO2 + Cl2    SO2Cl2 (sulphuryl chloride)
Sun light

SO2 + O2 SO3 ; PbO2 + SO2  PbSO4

(vi) Reducing Nature :
H2O + SO2  H2SO3 ; H2SO3 + H2O  H2SO4 + 2H
 Reducing character is due to the liberation of nascent hydrogen
(a) Reduces halogens to corresponding halides
SO2 + 2H2O  H2SO4 + 2H
2H + Cl2  2HCl
––––––––––––––––––––––––––––––––
SO2 + 2H2O + Cl2  H2SO4 + 2HCl

(b) Reduces acidified iodates to iodine

SO2 + 2H2O  H2SO4 + 2H] × 5
2KIO3 + H2SO4  K2SO4 + 2HIO3
2HIO3 + 10H  I2 + 6H2O
––––––––––––––––––––––––––––––––––––––––––
2KIO3 + 5SO2 + 4H2O  K2SO4 + 4H2SO4 + I2
 It also reduces acidified KMnO4  Mn2+ (decolourises),
Acidified K2Cr2O7  Cr3+ (green coloured solution) & Ferric Sulphate  Ferrous sulphate
(vii) Oxidising nature :
Acts as oxidising agent with strong reducing agent
(a) 2H2S + SO2   2H2O + 3S
moisture

(b) 2SnCl2 + SO2 + 4HCl  2SnCl4 + 2H2O + S

(c) 2Hg2Cl2 + SO2 + 4HCl  2HgCl2 + 2H2O + S
(d) 2CO + SO2  2CO2 + S
(e) 2 Fe + SO2  2FeO + FeS
(viii) Bleaching Action :
SO2 + 2H2O  H2SO4 + 2H
This is due to the reducing nature of SO2
Coloured matter + H colourless matter..
Air oxidation
Therefore, bleaching is temporary
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USES :
(i) Used in manufacture of H2SO4 & paper from wood pulp.
(ii) As a bleaching agent for delicate articles like wool, silk and straw.
(iii) Used in refining of petroleum and sugar.

(D) SULPHUR TRIOXIDE (SO3) :

PREPARATION:

(i) 6H2SO4 + P4O10  6SO3 + 4H3PO4

 P4O10 is dehydrating agent
(ii) 
Fe2(SO4)3  Fe2O3 + 3SO3

(iii) 2SO2 + O2 2SO3

PROPERTIES:
(i) Acidic Nature :
Dissolves in water forming sulphuric acid
SO3 + H2O  H2SO4
(ii) H2SO4 + SO3  H2S2O7 (oleum)
(iii) SO3 + HCl  SO2(OH) Cl (chlorosulphuric acid)
(iv) Oxidising Nature :
0
(a) 2SO3 + S  
 3SO2
100 C

(b) 5SO3 + 2P  5SO2 + P2O5

(c) SO3 + PCl5  POCl3 + SO2 + Cl2
(d) SO3 + 2HBr  H2O + Br2 + SO2

USES:
(i) Used in manufacture of H2SO4 and oleum.
(ii) Used as a drying agent for gases.

(E) SULPHURIC ACID (H2SO4) :

PREPARATION:
(i) 2FeSO4 . 7H2O   Fe2O3 + H2SO4 + SO2 + 13H2O
dist .

(ii) Lead Chamber Process (Industrial method) :

2SO2 + O2 (air) + 2H2O + [NO] (catalyst)  2H2SO4 + [NO] (catalyst)
Acid obtained is 80% pure and is known as brown oil of vitriol
(iii) Contact process (Industrial method) :
O2 + 2SO2 2SO3
The commonly used catalysts are platinum, ferric oxide or vanadium pentoxide. V2O5 is preferred as it is cheaper and is not
poisoned by impurities
H2SO4 (58%) + SO3  H2S2O7 (oleum)
Sulphuric acid of any desired concentration can be obtained from oleum by dilution with water.
H2S2O7 + H2O  2H2SO4
Oxidation of sulphur dioxide is reversible and exothermic. According to Le-chatelier principle, the favourable conditions for
the greater yield of sulphur trioxide are.
(a) An excess of air- SO2 and oxygen are taken in 2:3 molecular proportion
(b) Low tempt-optimum tempt. 4500C
(c) Higher pressure-one atmosphere
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PROPERTIES :
(i) A colourless syrupy liquid (it is H-bonded)
(ii) It fumes strongly in moist air and is highly corrosive in nature.
(iii) Thermal decomposition :
H2SO4 H2O + SO3
(iv) Acidic Nature :
It is a strong dibasic acid and ionises as
H2SO4 H+ + HSO4– 2H+ + SO42–
(a) Forms two series of salts
NaOH + H2SO4  NaHSO4 (sodium bisulphate) + H2O
NaHSO4 + NaOH  Na2SO4 (sodium sulphate) + H2O
(b) Decomposes carbonates and bicarbonates into carbon dioxide
Na2CO3 + H2SO4  Na2SO4 + H2O + CO2
NaHCO3 + H2SO4  NaHSO4 + H2O + CO2
(c) Displaces more volatile acids from their metal salts.
2NaCl + H2SO4  Na2SO4 + HCl
2NaNO3 + H2SO4  Na2SO4 + 2HNO3
CaF2 + H2SO4  CaSO4 + 2HF
(v) Oxidising Nature :
H2SO4 acts as a strong oxidising agent
2H2SO4 + 2e–  SO42– + 2H2O + SO2
or
H2SO4  H2O + SO2 + [O]
(a) Non-metals (carbon, sulphur etc) are oxidised to their oxides.
H2SO4  H2O + SO2 + O] × 2
C + 2[O]  CO2
––––––––––––––––––––––––––––––––––––
C + 2H2SO4  CO2 + 2SO2 + 2H2O
––––––––––––––––––––––––––––––––––––
2P + 5H2SO4  2H3PO4 + 5SO2 + 2H2O
(b) Metals (copper, silver, mercury etc.) are oxidised to their oxides which then combine with acid to form corresponding
sulphates.
H2SO4  H2O + SO2 + [O]
Cu + [O]  CuO
CuO + H2SO4  CuSO4 + H2O
–––––––––––––––––––––––––––––––––
Cu + 2H2SO4  CuSO4 + SO2 + 2H2O
(c) Iodine is liberated from KI
2 KI + H2SO4  K2SO4 + 2HI
H2SO4  H2O + SO2 + [O]
2 HI + [O]  I2 + H2O
–––––––––––––––––––––––––––––––––––––
2 KI + 2H2SO4  K2SO4 + SO2 + I2 + 2H2O
Here HI is oxidised to I2. Similarly bromine is liberated from KBr

(d) C10H8 (naphthalene) + 9H2SO4 C8H6O4 (phthalic acid) + 10H2O + 9SO2 + 2CO2
 p-BLOCK ELEMENTS

(vi) Dehydrating agent :

Sulphuric acid acts as a powerful dehydrating agent because it has a great affinity for water

(a) C12H22O11 (cane sugar) 12C

(b)    CO + CO2 + H2O

H2SO 4


(vii) Miscellaneous reactions :

(a) Sulphonation of aromatic compounds

+ H2SO4  + H2O

Benzene Benzene sulphonic acid

(b) Reaction with PCl5 :
OH Cl
O2S + PCl5  O2S + POCl3 + HCl
OH OH
Chlorosulphonic acid
OH Cl
O2S + 2PCl5  O2S + 2 POCl3 + 2HCl
OH Cl
Sulphury chloride
(c) K4[Fe(CN)6] + 6H2SO4 + 6H2O  2K2SO4 + FeSO4 + 3(NH4)2SO4 + 6CO
(d) 
3KClO3 + 3H2SO4  3 KHSO4 + HClO4 + 2ClO2 + H2O
(e) H2SO4 + P2O5  2HPO3 + SO3
USES :
(i) For the manufacture of fertilizer such as ammonium sulphate and super phosphate of lime.
(ii) As an important laboratory reagent.
(iii) In storage batteries.
(iv) In leather, textile, paper and dyeing industries.
GROUP 17 ELEMENTS : THE HALOGEN FAMILY
Fluorine, chlorine, bromine, iodine and astatine are members of Group 17. These are collectively known as the halogens
(Greek halo means salt and genes born i.e., salt producers). The halogens are highly reactive non-metallic elements.
Electronic Configuration :
All these elements have seven electrons in their outermost shell (ns2 np5) which is one electron short of the next noble gas.
Atomic and Ionic Radii :
The halogens have the smallest atomic radii in their respective periods due to maximum effective nuclear charge . Atomic
and ionic radii increase from fluorine to iodine due to increasing number of quantum shells.
Ionisation Enthalpy :
They have little tendency to lose electron. Thus they have very high ionisation enthalpy. Due to increase in atomic size,
ionisation enthalpy dereases down the group.
Electron Gain Enthalpy :
Halogen have maximum negative electrons gain enthalpy in the corresponding period. This is due to the fact that the atoms
of these elements have only one electron less than stable noble gas configurations. Electron gain enthalpy of the elements of
the group becomes less negative down the group. However, the negative electron gain enthalpy of fluorine is less than that of
chlorine. It is due to small size of fluorine atom. As a result, there are strong interelectronic repulsions in the relatively small
2p orbitals of fluorine and thus, the incoming electron does not experience much attraction.
 p-BLOCK ELEMENTS

Electronegativity :
They have very high electronegativity. The electronegativity decreases down the group. Fluorine is the most electronegative
element in the periodic table
Physical Properties :
Fluorine and chlorine are gases, bromine is a liquid and iodine is a solid. Their melting and boiling points steadily increase
with atomic number. All halogen are coloured. This is due to absorption of radiations in visible region which results in the
excitation of outer electrons to higher energy level. By absorbing different quanta of radiation, they display different colours.
For example, F2, has yellow, Cl2, greenish yellow, Br2, red and I2, violet colour. Fluorine and chlorine react with water.
Bromine and iodine are only sparingly soluble in water. But are soluble in organic solvents such as chloroform, carbon
tetrachloride, carbon disulphide and hydrocarbons to give coloured solutions.Except the smaller enthalpy of dissociation of
F2 compared to that of Cl2 whereas X-X bond dissocitation enthalpies from chlorine onwards show the expected trend: Cl –
Cl > Br – Br > I – I . A reason for this anomaly is the relatively larger electrons- electron repulsion among the lone pairs in
F2 molecule where they are much closer to each other than in case of Cl2.

ATOMIC & PHYSICAL PROPERTIES :

Element F Cl Br I
Atomic Number 9 17 35 53
Atomic Mass 19 35.45 79.90 126.90
2 5 2 5 10 2 5
Electronic configuration [He] 2s 2p [Ne] 3s 3p [Ar] 3d 4s 4p [Kr] 4d105s2 5p5
Covalent Radius / pm 64 99 114 133
–
Ionic Radius X / pm 133 184 196 220
–1
Ionization enthalpy / (kJ mol ) 1680 1256 1142 1008
–1
Electron gain enthalpy /(kJ mol ) – 333 – 349 – 325 – 296
Distance X -X/pm 143 199 229 266
–1
Enthalpy of dissociation (X2)/kJ mol 158.8 242.6 192.8 151.1
Electronegativity 4 3.2 3.0 2.7
Melting point / K 54.4 172 265.8 386.6
Boiling point / K 84.9 239.0 332.5 458.2

Chemical Properties
Oxidation states and trends in chemical reactivity
All the halogens exhibit –1 oxidation state. However, chlorine, bromine and iodine exhibit + 1, + 3, + 5 and + 7 oxidation
states also. The higher oxidation states of chlorine, bromine and iodine are realised mainly when the halogens are in combi-
nation with the small and highly electronegative fluorine and oxygen atoms e.g., in interhalogens, oxides and oxoacids.
The fluorine atom has no d orbitals in its valence shell and therefore cannot expand its octet. Being the most electronegative,
it exhibits only – 1 oxidation state.
All the halogens are highly reactive. They react with metals and non-metals to form halides. The reactivity of the halogens
decreases down the group.
The ready acceptance of an electron is the reason for the strong oxidising nature of halogens. F2 is the strongest oxidising
halogen and it oxidises other halide ions in solution or even in the solid phase. The decreasing oxidising ability of the
halogen in aqueous solution down the group is evident from their standard electrode potentials. Fluorine oxidises water to
oxygen whereas chlorine and bromine react with water to form corresponding hydrohalic and hypohalous acids. The reac-
tions of iodine with water is non- spontaneous . I– can be oxidised by oxygen in acidic medium; just the reverse of the
reaction observed with fluorine.
2F2(g) + 2H2O()  4H+ (aq) + 4F– (aq) + O2(g)
X2(g) + H2O ()  HX(aq) + HOX (aq)
(where X = Cl or Br)
4I– (aq) + 4H+ (aq) + O2(g)  2 I2 (s) + 2H2O ()
 p-BLOCK ELEMENTS

Standard Reduction Potential (SRP)

X + 2e–  2X–
2

F2 + 2e–  2F– ° = + 2.87 V ; Cl2 + 2e–  2Cl– ° = + 1.36 V

Br2 + 2e –  2Br – ° = + 1.09 V ; 2 + 2e–  2– ° = + 0.54 V

 More the value of the SRP, more powerful is the (algebraically) oxidising agent. Hence the order of oxidising power is F2 >
Cl2 > Br2 > 2
Since SRP is the highest for F2 (among all elements of P.T.), it is a strogenst oxidising agent.
 F2 is more powerful oxidising agent than O3 [Inspite of 3 ‘O’s in O3 ]
Note : E.A. and .E. values pertain to atoms in gas phase where as redox phenomena occurs in gaseous medium.
Hence properties in the gas phase cannot reflect parallely in solution phase.
Electrode potential values would be the monitoring parameter in solution phase because they are experimental (based on the
correct situation).
Hydration energy of X–
Smaller the ion, higher is the hydration energy
F– Cl – Br – –
515 kJ/mol 381 347 305
Anomalous behaviour of fluorine :
The anomalous behviour of fluorine is due to its small size, highest electronegativity, low F- F bond dissociation enthalpy,
and non availability of d orbitals in valence shell. Most of the reactions of fluorine are exothermic (due to the small and
strong bond formed by it with other elements). It forms only one oxoacid while other halogen form a number of oxoacids.
Hydrogen fluoride is liquid (b.p. 293 K) due to strong hydrogen bonding. Other hydrogen halides are gases.
(i) Reactivity towards hydrogen:
They all react with hydrogen to give hydrogen halides but affinity for hydrogen decreases from fluorine to iodine. They
dissolve in water to form hydrohalic acids. The acidic strength of these acids varies in the order : HF < HCl < HBr < HI. The
stability of these halides dereases down the group due to decrease in bond (H–X) dissociation enthalpy in the order :
H – F > H – Cl > H –Br > H – I .
(ii) Reactivity towards oxygen :
Halogens form many oxides with oxygen but most of them are unstable. Fluorine forms two oxides OF2 and O2F2. However,
only OF2 is the thermally stable at 298 K. These oxide are essentially oxygen fluorides because of the higher electronegativ-
ity of flurorine than oxygen . Both are strong fluorinating agents. O2F2 oxidises plutonium to PuF6 and the reactions is used
in removing plutonium as PuF6 from spent nuclear fuel.
Chlorine, bromine and iodine form oxides in which the oxidation states of these halogen range from + 1 to + 7. A combina-
tion of kinetic and thermodynamic factors lead to the generally decreasing order of stability oxides formed by halogens,
I > Cl > Br. The higher oxides of halogens tend to be more stable than the lower ones.
Chlorine oxides, Cl2O, ClO2, Cl2O6 and Cl2O7 are highly reactive oxidising agents and tend to explode. ClO2 is used as a
bleaching agent for paper pulp and textiles and in water treatment.
The bromine oxides, Br2O, BrO2, BrO3 are the least stable halogen oxides and exist only at low temperature. They are very
powerful oxidising agents.
The iodine oxides, I2O4, I2O5, I2O7 are insoluble solids and decompose on heating. I2O5 is very good oxidising agent and is
used in the estimation of carbon monoxide.
(iii) Reactivity towards metals:
Halogen react with metals to form metal halides. For e.g., bromine reacts with magnesium to give magnesium bromide.
(iv) Reactivity of halogen towards other halogens :
Halogens combine amongst themselves to form a number of compounds known as interhalogen of the types AB, AB3, AB5
and AB7 where A is a larger size halogen and and B is smaller size halogen.
 p-BLOCK ELEMENTS

1. FLUORINE (F2) :
PREPARATION:
(i) Electrolytic method :
Electrolyte : Molten KHF2 (1 part) + HF (5 part)
Anode : Carbon
Cathode : Steel
Vessel : Monel metal

On Electrolysis
Cathode : 2H+ + 2e–  H2(g)
Anode : 2F–  F2 + 2e–
The F2 gas thus evolved must be free from HF which is more corrosive than fluorine.
In order to make flourine free from HF, the gas is passed through NaF which absorbs HF.

 Anode of carbon should be free from graphide because F2 reacts with graphite easily to form a polymeric susbstance known
as graphite fluoride.
There should be no moisture present in the vessel otherewise fluorine will react with water.
3H O + 3F  6HF + O ;
2 2 3
2F + 2H O  4HF + O
2 2 2
 It is not possible to prepare fluorine by electrolysis of aq. solution of NaF or KF. It is because when aq. solution of KF is
subjected to electrolysis, there will be following two oxidation in competition at anode,
H O  1/2O + 2H+ + 2e–
2 2
SOP = – 1.23 v
and
F  1/2F2 + e
– –
SOP = – 2.87v
As a matter of rule that substance will be oxidise whose SOP is higher therefore water gets oxidise at anode and not F–.
(ii) Chemical method : From K2 [MnF6] - potassium hexafluoromanganate (IV)

1  via 1 
K2 [MnF6] + 2 SbF5  2K [SbF6] + MnF3 + F2 ; MnF4  MnF3  F2 
2  2 

 In this reaction, the stronger Lewis acid SbF5 displaces the weaker one, MnF4 from its salt. MnF4 is unstable and readily

decomposes to give MnF3 and fluorine.

PROPERTIES :
(i) Diatomic, Pale green-yellow gas which appears to be almost colourless. It is heavier then air. It condenses to yellow liquid at
– 188 0C and yellow solute at – 2230C. It has punged oddur and is highly poisonous.
(ii) Oxidising character : It is the most powerful oxidising agent.
F + 2NaX  2NaF + X
2 2
(X = Cl, Br, )
(a) It can oxidise all other halide ions into halogen molecules
5 7
(b) It can oxidise Cl O 3 into Cl O 4 and IO3– to IO4–

F2 + ClO3– + H2O  2F– + ClO4– + 2H+

(c) It can oxidise HSO4– into S2O82–
( 6 ) ( 6 )
2H SO 4 + F2  2F– + S 2 O 2 + 2H+
8
 Some of the O2– changes to O– in the persulphate ions (having the O–). Hence oxygen is getting oxidised.
 p-BLOCK ELEMENTS

(iii) Reaction with NaOH solution : With dilute alkali forms oxygen difluoride and with concentrated alkali O2.
2F2 + 2 NaOH (dil)  OF2 (g) + 2 NaF + H2O
2F2 + 4 NaOH (conc.)  O2 (g) + 4 NaF + 2H2O
(iv) Reaction with NH3 : (Distinction from other halogens)
2NH + 3F  N + 6 HF
3 2 2

 Other halogens form explosive NX3. with conc. NH3 (liquor ammonia)
(v) Reaction with H2S :
H S + F  SF + 2 HF
2 2 6

 H2S burns
(vi) Reaction with SiO2 : It attacks glass at about 1000C.
SiO2 (s) + 2F2 (g)  SiF4 (g) + O2 (g)
The reaction is slow with dry F2 .
(vii) Reaction with H2O :
2H2O + 2F2  4 HF + O2
sometime a little amount of O3 also forms
3H2O + 3F2  6HF + O3

(viii) Reaction with Xe :

(ix) Reaction with H2 :

H2 + F2  2 HF or H2 F2

 This reactions occurs even in dark

(x) Reaction with SO3 :

SO3 + F2   FSO OOSO F

180 º C
AgF 2 2

(xi) Reaction with O2 :

only in presence of
O2 + F2          O2F2
silent electric disch arg e

(xii) Reaction with metals and non–metals : It combines with most of the metals. Almost all non-metals except O2 & N2 ignite
spontaneously in presence of F2 .
2 Ag + F2  2 AgF ; 2 Al + 3 F2  2 AlF3
C + 2 F2  CF4 ; Si + 2 F2  SiF4

2. CHLORINE (Cl2) :
PREPARATION:
(i) Common method (Cl2 , Br2 , 2) :

2 NaX + 3H2SO4 (conc.) + MnO2 (oxidising agent)  X2 + MnSO4 + 2NaHSO4 + 2H2O
4H+ + MnO2 + 2X–  X2 + Mn+2 + 2H2O
 p-BLOCK ELEMENTS

(ii) Only for Cl2 :

(a) NaCl + HNO3  NaNO3 + HCl × 3
HNO3 + 3HCl  NOCl + Cl2 + 2H2O
––––––––––––––––––––––––––––––––––––
3NaCl + 4 HNO3  3 NaNO3 + NOCl (nitrosyl chloride) + Cl2 + 2H2O
2NOCl + O2  2NO2 + Cl2 ; NO2 + H2O  HNO3 (to be recycled)
(b) When Cl2 is used for the chlorination of hydrocarbon the byproduct is HCl. The HCl is catalytically oxidised into H2O & Cl2
using copper powder mixed with rare earth chlorides.
Cu powder  rare earth
4 HCl + O2            2H O + 2Cl
Chloride 2 2

OCl
(c) Ca + 2HCl  CaCl2 + Cl2 + H2O
Cl
(d) 2KMnO4 + 16 HCl  2 KCl + 2 MnCl2 + 5 Cl2 + 8 H2O

(e) PbO2 + 4 HCl  PbCl2, + Cl2 + 2 H2O

(iii) Manufacture of chlorine :
(a) Deacon’s process : By oxidation of hydrogen chloride gas by atmoshperic oxygen in the presence of CuCl2 (catalyst) at 723
K.
4 HCl + O2   2 Cl2 + 2 H2O
CuCl 2

(b) Electrolytic process : Chlorine is obtained by the electrolysis of brine (concentrated NaCl solution). Chlorine is liberated at
anode. It is also obtained as a by–product in many chemical industries.
NaX (aq)  Na+ (aq) + X– (aq)
Anode : 2X–  X2 + 2e–
PROPERTIES :
(i) It is a greenish–yellow gas with pungent and suffocating odour. It is about 2–5 times heavier than air. It can be liquefied into
greenish–yellow liquid which boils at 239 K. It is soluble in water.
(ii) At low temperature it forms a hydrate with water having formula Cl2 . 8H2O which is infact a clathrate compound.
(iii) H2 + Cl2           2HCl (g) , [H2 + Br2  2HBr is not a zero order reaction]
(a zero order reaction)
(iv) Reaction with NH3 (common for Cl2 & Br2) :

(a) 8 NH3 + 3 Cl2  N2 + 6 NH4 Cl

(b) NH3 + 3Cl2  NCl3 + 3 HCl
(excess)
(v) Reaction with alkali metal halides (KX) :
2 KBr + Cl2  2KCl + Br2
2K + Cl2  2 KCl + 2

 Cl2 can oxidise both Br– & – but Br2 can oxidise – only.

 F2 is not used in aqueous reaction since it itself reacts with water.

(vi) Oxidising & bleaching properties : Chlorine water on standing loses its yellow colour due to the formation of HCl and
HOCl. Hypochlorous acid (HOCl) so formed, gives nascent oxygen which is responsible for oxidising and bleaching properties
of chlorine.
 p-BLOCK ELEMENTS

(i) It oxidises ferrous to ferric, sulphite to sulphate, sulphur dioxide to sulphuric acid and iodine to iodic acid.
2 FeSO4 + H2SO4 + Cl2  Fe2(SO4)3 + 2 HCl
Na2SO3 + Cl2 + H2O  Na2SO4 + 2 HCl
SO2 + 2 H2O + Cl2  H2SO4 + 2 HCl
I2 + 6 H2O + 5 Cl2  2 HIO3 + 10 HCl
(ii) It is a powerful bleaching agent ; Bleaching action is due to oxidation.
Cl2 + H2O  2 HCl + O
Coloured substance + O  Colourless substance
It bleaches vegetable or organic matter in the presence of moisture. Bleaching effect of chloride is permanent.
 But the bleching action of SO2 is temporary because it takes place through reduction.
SO2 + 2 H2O  H2 SO4 + 2 H
SO32– + Coloured material  SO42– + Reduced coloured material (colourless)
O2 of air
Reduced Coloured material (colourless)    Coloured material
(vii) Reaction with NaOH :
Common to Br2 , 2 & Cl2 (but with F2 it is different, OF2 or O2 is obtained)
(a) 2 NaOH ( cold & dilute) + Cl2  NaCl + NaClO + H2O
(b) 6 NaOH (hot & concentrated) + 3 Cl2  5 NaCl + NaClO3 + 3 H2O
(viii) Reaction with Hypo solution :
This reaction is common with Cl2 & Br2 but with 2 it is different.
( 2 ) ( 2 ) (o)
Na2 S 2 O3 + H2O + Cl2  Na2 SO 4 + 2HCl + S (colloidal)
In this reaction thiosulphate ions undergo disproportionation into SO42– and S. Cl2 is reduced to Cl– .
(ix) Reaction with dry slaked lime, Ca(OH)2 : It gives bleaching powder.
2 Ca(OH)2 + 2 Cl2  Ca(OCl)2 + CaCl2 + 2 H2O
(x) Reaction with metals & non–metals : Forms corresponding chlorides.
2 Al + 3 Cl2  2 AlCl3 ; 2 Na + Cl2  2 NaCl
P4 + 6 Cl2  4 PCl3 ; S8 + 4 Cl2  4 S2Cl2
 It has great affinity for hydrogen. It reacts with compounds containing hydrogen to form HCl.
H2 + Cl2  2 HCl ; H2S + Cl2  2 HCl + S ; C10H16 + 8 Cl2  16 HCl + 10 C
Uses : Cl2 is used
(i) for bleaching woodpulp (required for the manufacture of paper and rayon). bleaching cotton and textiles,
(ii) in the manufacture of dyes, drugs and organic compounds such as CCl4 , CHCl3 , DDT, refrigerants, etc.
(iii) in the extraction of gold and platinum.
(iv) in sterilising drinking water and
(v) preparation of poisonous gases such as phosgene (COCl2), tear gas (CCl3NO2), mustard gas (ClCH2CH2SCH2CH2Cl).

3. BROMINE (Br2) :
PREPARATION:
(i) Common method :
2 NaBr + 3H2SO4 (conc.) + MnO2   Br + MnSO + 2NaHSO + 2H O
2 4 4 2
(ii) From Sea-water :
NaCl is main component but NaBr is also present in some quantity in sea water. Cl2 gas is passed through sea water when
vapours of bromine are evolved.
2 Br– (aq) + Cl  2Cl– (aq.) + Br
2 2
 p-BLOCK ELEMENTS

PROPERTIES :
(i) Reddish brown liquid, fairly soluble in water. It also forms hydrate like Cl2
(Br2 . 8H2O)  Clathrate compound
(ii) Rest reactions are same as with Cl2

4. IODINE (I2) :
PREPARATION:
(i) Common method :
2Na + 3H2SO4 (conc.) + MnO2   2 + MnSO4 + 2NaHSO4 + 2H2O
(ii) From Caliche or Crude chile salt petre :
The main source of iodine is NaO3 (sodium iodate) which is found in nature with NaNO3 (chile saltpetre). NaO3 is present
in small amount. After crystallisation of NaNO3 , the mother liquor left contains NaO3 (soluble). To this solution NaHSO3
is added where upon 2 is precipitated.
2O3– + 5HSO3–  3 HSO4– + 2SO42– + 2 (s) + H2O
(iii) From sea-weeds :
Sea-weeds are dried and burnt in shallow pits, ash left is called kelp. Ash on extraction with hot water dissolves out chlorides,
carbonates, sulphates and iodides of sodium and potassium. The solution on concentration seperates out all leaving behind
iodide in the solution. Solution is mixed with MnO2 and concentrated H2SO4 in iron retorts. Liberated iodine is condensed in
series of earthen-ware known as aludels.
2Na+ MnO + 3H SO  2NaHSO + MnSO +  + 2H O
2 2 4 4 4 2 2
(iv) 2K+ Cl2  2KCl + 2 (v) 2K+ H2O2  2KOH + 2
(vi) CuSO4 + 2K  K2SO4 + Cu2 ; 2Cu2  Cu22 + 2

 This 2 gets dissolved into K forming 3 , since 3– ions are yellow, therefore solution develops yellow colour.
PROPERTIES :
(i) It is a dark violet solid, undergoes sublimation, least soluble (among halogens) in water but much more soluble in K(aq.) due
to formation of K3
 KF3 cannot be formed similarly since F does not have ‘d’ orbitals. So sp3d hybridisation is not possible with F.
(ii) It is soluble in organic solvents like CHCl3, CCl4 etc. to get violet solutions.
(iii) Reaction with hypo :
iodometric titrations
2.5
S2 O32– (thiosulphate ions) + 2  S 4 O 26 (tetrathionate ions) + 2
–

This reaction is the basis of iodometric (direct 2 titration) titration, which is carried out for the estimation of iodine using
starch indicator.
(iv) Reaction with NH3 :
NH (g) +   No Reaction
3 2

NH 3 (aq) +  2 (s) N 3 . NH 3 + 3H 
A slurry is formed
(Ammonia liquor) which can be dried an explosive
and on hammering it (Nitrogentriiodide
explodes causing ammoniated)
sound (crakers)

8N3. NH3  5N2 + 9 2 + 6NH4

(v) Reaction with KClO3 or KBrO3 :

2 KClO3 + 2  
2 KIO3 + Cl2 ; 2 KBrO3 + 2  2KIO3 + Br2
 p-BLOCK ELEMENTS

(vi) Reaction with ozone (dry) :

22 (s) + 3O3 (g)  4O9 (s)
4O9 is an ionic compound consisting of 3+ & O3–)3 indicative of metallic character of  (low .E, low E.N.)
 With NaOH there is common reaction as with Cl2 and Br2 . With H2 there is reversible reaction.
OXIDES OF CHLORINE :
Chlorine dioxide (ClO2 ) :
PREPARATION:

H 2ClO (g) + SO 2– (aq)
(i) 2 ClO3– (aq) + SO2 (g)  2 4

 Chlorates of sodium and potassium can be used

(ii) 2KClO3 + 2 H2C2O4   2 Cl O 2 (g) + 2CO2 + K2C2O4 + 2H2O

90 º C

(iii) 2AgClO3 + Cl2   2AgCl  (white) + 2ClO2 + O2

90 º C

(iv) Cl2O6 + N2O4 ClO2 + [NO2+] [ClO4–]

PROPERTIES :
(i) Yellow gas at room temp, soluble in water and explosive substance. It also behaves as an oxidising agent. (It kill bacteria
better than Cl2)

H Cl O (yellow solid) + 2O
(ii) Reaction with ozone : 2ClO2 + 2O3  2 6 2
dichlorine hexa oxide
In the reaction O3 is behaving as an oxidising agent.
 Cl2O6 (s) is a mixed anhydride of HClO3 & HClO4 because on dissolving in water it gives a mixture of these two acids.
 In solid state, Cl2O6 exists as ClO2+ & ClO4–.

(iii) Reaction with alkaline H2O2 :

In this reaction H2 O2 acts as a reducing agent. It reduces ClO2 into ClO2–
H2O2  2H+ + O2 + 2e– ; e– + ClO2  ClO2– ] × 2
–––––––––––––––––––––––––––––––––––––––––––––––––
H O + 2ClO  2ClO – + 2H+ + O
2 2 2 2 2
–––––––––––––––––––––––––––––––––––––––––––––––––
or H O + 2ClO + 2OH–  2ClO – + 2H O + O
2 2 2 2 2 2
(iv) Reaction with H :
In this reaction H behaves as a reducing agent where it reduces ClO2 into Cl– and itself is oxidised to 2 .
[5e– + 4 H+ + ClO2  Cl– + 2H2O] × 2
[2–  2 + 2e–] × 5
–––––––––––––––––––––––––––––––––––––––––––
2ClO + 8H+ + 10 –  5I + 2Cl– + 4H O
2 2 2
HYDRA ACIDS (HALOGEN ACIDS) :
HCl, HBr & HI :
PREPARATION:
(i) By direct combination of elements :
H + Cl  2HCl
2 2

Pt
H2 + Br2 
 2HBr
Pt , 450 C
H2 + 2     2H
 p-BLOCK ELEMENTS

(ii) By heating a halide with acid :

NaCl + H2SO4  NaHSO4 + HCl
NaHSO4 + NaCl  Na2SO4 + HCl
For HCl we use H2SO4 as an acid, while for HBr and H we use H3PO4.
(a) HCl cannot be dried over P2O5 (P4O10) or quick lime since they react with gas chemically.
CaO + 2HCl  CaCl2 + H2O
P4O10 + 3HCl  POCl3 + 3HPO3
HCl is, hence dried by passing through conc. H2SO4 .
(b) HBr (or H) cannot be prepared by heating bromide (iodide) with conc. H2SO4 because HBr and H are strong
reducing agents and reduce H2SO4 to SO2 and get themselves oxidised to bromine and iodine respectively.
KX + H2SO4  KHSO4 + HX
H2SO4 + 2HX  SO2 + X2 + 2H2O (X = Br or )
Hence, HBr and H are prepared by heating bromides and iodides respectively with conc. H3PO4 .
3KBr(K) + H3PO4  K3PO4 + 3HBr (H)
(iii) By reaction of P4 (Laboratory Method) :
P4 + 6Br2 (62)  4PBr3 (4P3) (product in situ)
PBr3 (P3) + 3H2O  3HBr (H) + H3PO3
(iv) By passing H2S / SO2 into solutions of halogens :
H2S + X2  2HX + S
SO2 + 2H2O + X2  2HX + H2SO4

PROPERTIES :
(i) These are colourless, pungent smelling gases with acidic tastes.
(ii) It is heavier than air, can be liquified to colourless liquids.
(iii) These are neither combustible nor supporter of combustion.
(iv) When perfectly dry, they have no action on litmus, but in presence of moisture, they turn blue litumus red, showing acidic
nature. Among HX, H is the strongest and HF is the weakest acid.
(v) These are quite soluble in water.
HCl ionises as below.
HCl(g) + H2O ()  H3O+ (aq) + Cl– (aq) Ka = 107
It aqueous solution is called hydrochloric acid. High value of dissociation constant (Ka) indicates that it is a strong acid in
water.
When three parts of concentrated HCl and one part of concentrated HNO3 are mixed, aqua regia is formed which is used for
dissolving noble metals, e.g., gold, platinum.
Au + 4 H+ + NO3– + 4 Cl–  AuCl4– + NO + 2 H2O
3 Pt + 16 H+ + 4 NO3– + 18 Cl–  3 PtCl62– + 4 NO + 8 H2O
(v) Reaction with metals oxides, hydroxides and bicarbonates
Zn + 2HCl  ZnCl + H ; 2 2
MgO + 2HCl  MgCl + H O 2 2

NaOH + HCl  NaCl + H2O ;CaCO3 + 2HCl  CaCl2 + H2O + CO2
(vi) Reaction with salts, HCl decomposes salts of weaker acids.
NaHCO + HCl  NaCl + CO  + H O ;
3 2 2
Na2S + 2HCl  2NaCl + H2S
Na2SO3 + 2HCl  2NaCl + SO2 + H2O ; Na2S2O3 + HCl  2NaCl + SO2 + H2O + S
2NaNO2 + 2HCl  2NaCl + NO + NO2 + H2O
 p-BLOCK ELEMENTS

(vii) Reducing property and stability of hydracids :

HCl : It is quite stable and hence is oxidised by strong oxidising agents like MnO 2 , KMnO 4 , K 2 Cr 2 O 7 ,
PbO2, Pb3O4 .
(i) MnO2 + 4HCl  MnCl2 + 2H2O + Cl2
(ii) 2KMnO4 + 16HCl  2KCl + 2MnCl2 + 8H2O + 5Cl2
(iii) K2Cr2O7 + 14HCl  2KCl + 2CrCl3 + 7H2O + 3Cl2
(iv) PbO2 + 4HCl  PbCl2 + 2H2O + Cl2 ; (v) Pb3 O4 + 8HCl  3PbCl2 + 4H2O + Cl2
Therefore, HCl is a weak reducing agent.
HBr : It is not very stable and hence more easily oxidised or acts as a strong reducing agents. In addition
to above reducing properties of HCl, it also reduces H2SO4 to SO2 which is not done by HCl.
H2SO4 + HBr  SO2 + Br2 + 2H2O
Aqueous HBr on exposure to atmospheric oxygen is oxidised to bromine (yellow)
4HBr + O  2 Br + 2H O
2 2 2
H : It is least stable hydrogen halide. It is readily oxidised and thus acts as a powerful reducing agent.
In addition to reaction shown by HCl, it shows following reactions also.
(a) H2SO4 + 2H  SO2 + 2 + H2O ; H2SO4 + 6H  S + 32 + 4H2O;
H2SO4 + 8H  H2S + 42 + 4H2O ;
(b) 2HNO3 + 2H  2NO2 + 2 + 2H2O (c) 2HNO2 + 2H  2NO + 2 + 2H2O
(d) HO3 + 5H  32 + 2H2O (e) K2S2O8 + 2H  K2SO4 + 2 + H2SO4
(f) 2FeCl + 2H  2FeCl +  + 2HCl
3 2 2
 Aqueous solution of acid, if exposed to O2 is oxidised to iodine.
4H + O2  22 + 2H2O
(viii) Reaction with ammonia :
NH3 + HX  NH4X (white fumes) (where X = Cl, Br, )

(ix) Action of halogens :

(a) Cl2 is liberated from HCl by F2 alone.
F2 + HCl  2HF + Cl2
(b) Br2 is liberated from HBr by F2 and Cl2 (not by 2)
2HBr + F2 / Cl2  2HF (2HCl) + Br2
(c) 2 is liberated from H by F2, Cl2 and Br2
2H + F2 (Cl2, Br2)  2HF (HCl, HBr) + 2
(x) Detection of cation:
HCl : AgNO3 + HCl  AgCl (white) + HNO3
(CH3COO)2 Pb + 2HCl  PbCl2(white) + 2CH3COOH
Hg(NO3)2 + 2HCl  Hg2 Cl2  (white) + 2HNO3
HBr : AgNO3 + HBr  AgBr (pale yellow) + HNO3
(CH3COO)2 Pb + 2HBr  PbBr2  (white) + 2CH3COOH
H: AgNO3 + H  Ag (bright yellow) + HNO3
(CH3COO)2 Pb + 2H  Pb2 (yellow) + 2CH3COOH
HgCl2 + 2H  Hg2 (scarlet red) + 2HCl
 p-BLOCK ELEMENTS

H reacts with CuSO4 liberating iodine via the formation of cupric iodide (not by HCl or HBr).
2CuSO4 + 4H  2Cu2 + 2H2SO4 ; 2Cu2  Cu2 2 + 2
(xi) Formation of aqua-regia :
3 parts of conc. HCl and 1 part of conc. HNO 3 is known as aqua-regia. This is used for dissolving
noble metals like Au (Gold) and Pt (Platinum).
3HCl + HNO  NOCl + 2H O + 2Cl (reactive) ;
3 2
Au + 3Cl  AuCl 3

USES :
(i) HCl is used in preparation of Cl2, chlorides, aqua regia, glucose, (from corn starch), medicines, laboratory reagents, cleaning
metal surfaces before soldering or electroplating. It is also used for extracting glue from bones and purifying bone black.

(ii) HBr is used as laboratory reagent for preparing bromo derivatives like sodium bromides and potassium bromide. These are
used in medicines as sedatives.

(iii) H is used as reducing agent in organic chemistry.

HYDROFLUORIC ACID [H2 F2, HF] :
PREPARATION :
H2 and F2 combine with each other very violently (even in dark) to form HF. So simple reaction cannot be used for its
preparation, special methods are employed for its preparation.
(i) Laboratory Method :
Anhydrous HF is obtained by heating dry potassium hydrogen fluoride in a copper retort connected with copper condenser.


KHF2  KF + HF
(ii) Industrial Method :
HF is prepared by heating fluorspar (CaF2) with conc H2SO4.
CaF2 + H2SO4  CaSO4 + 2HF

 Aqueous HF being corrosive to glass, is stored in wax lined bottles or vessel made of copper or monel.
In glass or silica bottles, it attacks them as follows:
Na SiO + 6HF  Na SiF + 3H O ; CaSiO + 6HF  CaSiF + 3H O
2 3 2 6 2 3 6 2

SiO2 + 4HF  SiF4 + 2H2O ; SiF4 + 2HF  H2 SiF6

This action of HF on silica (silicates) is used for etching glass. The glass surface to be etched is coated with wax, the design,
is scratched on glass through wax coating this is then treated with 40% solution.
PROPERTIES:
(i) It is colourless, corrosive liquid with pungent smell with high boiling point due to hydrogen bonding.
(ii) Dry HF does not attack metals under ordinary conditions (except K), but in presence of water, it
dissolves metals with liberation of hydrogen gas.
(iii) It is a weak dibasic acid (due to strong HF bond) and forms two series of salt.
NaOH + H F  NaHF + H O ; NaHF + NaOH  2NaF + H O
2 2 2 2 2 2
(iv) Concentrated acid reacts with oxides, hydroxides and carbonates.
2NaOH + H2 F2  2NaF + 2H2O : CaCO3 + 2HF  CaF2 + H2O + CO2

OXY-ACIDS OF CHLORINE :
HYPO-CHLOROUS ACID [HClO] :
PREPARATION:
(i) The acid is known only in solution, It is obtained by shaking precipitate of HgO with chlorine water.
2HgO + 2Cl + H O  Hg OCl (Oxychloride of mercury) + 2HClO
2 2 2 2
 p-BLOCK ELEMENTS

(ii) Commercially, it is obtained by passing CO2 through suspension of bleaching powder and then distilling.
2CaOCl2 + H2O + CO2  CaCl2 + CaCO3 + 2HClO
PROPERTIES:
(i) It is a weak acid. Its concentrated solution is yellow in colour while dilute solution is colourless. It is unstable and decomposes.
2HClO  2HCl + O 2

(ii) It dissolves magnesium with evolution of hydrogen.

Mg + 3HClO  Mg(ClO) + H 2 2

(iii) With alkalies, it forms salts called hypochlorites.

(iv) It acts as a powerful oxidising and bleaching agent. This is due to release of nascent oxygen easily.
HClO  HCl + O

CHLOROUS ACID [HClO2] :

PREPARATION:

It is obtained in aqueous solution when barium chlorite suspension in water is treated with H2SO4 . The insoluble barium
sulphate is filtered off.
Ba(ClO ) + H SO  BaSO + 2HClO
2 2 2 4 4 2
PROPERTIES:
(i) The freshly prepared solution is colourless but it soon decomposes to ClO2 which makes the solution yellow.
5 HClO2  4 ClO2 + HCl + 2H2O
(ii) The acid undergoes auto-oxidation.
2HClO  HClO + HClO
2 3
(iii) The acid liberates iodine from K
4K + HClO2 + 2H2O  4KOH + HCl + 22

CHLORIC ACID [HClO3] :

PREPARATION:

This acid is only known in solutuion. The acid is preapred by the action of the dilute H2SO4 on barium chlorate.
Ba (ClO3)2 + H2SO4  BaSO4 + 2HClO3.

PROPERTIES:
Concentrated acid is colourless and pungent smelling liquid. It decomposes in light. However, it is stable in dark. It acts as
a strong oxidising and bleaching agent in light. Organic substances like paper, cotton, wool, etc., catch fire in contact with the
acid.

Per-Chloric Acid [HCIO4] :

PREPARATION:
It is the most stable oxy-acid of chlorine. Anhydrous HClO4 is obtained by doing distillation of KCIO4 (potassium perchlorate),
with 96-97.5% H2SO4 under low pressure at 90-160°C.
KCIO4 + H2SO4  KHSO4 + HCIO4
 p-BLOCK ELEMENTS

An aqueous solution of the acid is obtained by reacting barium perchlorate with calculated quantity of dilute H2SO4. The
insoluble barium sulphate is removed by filtration.
Ba(CIO4)2 + H2SO4  BaSO4  + 2HClO4

PROPERTIES:
(i) Anhydrous HClO4 is a colourless liquid which turns dark on keeping. It fumes in moist air.
(ii) It is one of the strongest acid and ionises as follows :
HClO  H+ + ClO –
4 4
(iii) It dissolves most of the metals.
Zn + 2HClO4  Zn(ClO4)2 + H2
(iv) It is an oxidising agent and explodes in contact with organic matter.
(v) 2HClO4 + P2O5  2HPO3 + Cl2O7

BLEACHING POWDER (CaOCl2.H2O)

Bleaching powder is also called calcium chlorohypochlorite because it is considered as a mixed salt of hydrochloric acid
and hypochlorous acid.
Ca(OCl)Cl
PREPARATION:

  Ca(OCl)Cl + H2O
0
40 C
Ca(OH)2 + Cl2
Properties
(i) It is a pale yellow powder. It has a strong smell of chlorine. It is soluble in water but a clear solution is never formed due to
the presence of impurities.
(ii) On long standing, it undergoes auto–oxidation into calcium chlorate and calcium chloride.
6 CaOCl2  Ca(CIO3)2 + 5 CaCl2
2 CaOCl2   2 CaCl2 + O2
CoCl
(iii) 2

(iv) In presence of a little amount of a dilute acid, it loses oxygen.

2 CaOCl2 + H2SO4  CaCl2 + CaSO4 + 2 HClO
HClO  HCl + O
On account of the liberation of nascent oxygen, it shows oxidising and bleaching properties.
(a) Oxidising properties
CaOCl2 + H2S  CaCl2 + H2O + S
CaOCl2 + 2 KI + 2 HCl  CaCl2 + 2 KCl + H2O + I2
3 CaOCl2 + 2 NH3  3 CaCl2 + 3 H2O + N2
 It oxidises NO2– to NO3– , AsO33– to AsO43– and Fe2+ to Fe3+ (in acidic medium)

(b) Bleaching action

Coloured matter + [O]  colourless product.
(v) When bleaching powder reacts with dilute acids or CO2 it liberates chlorine which is known as available chlorine.
CaOCl2 + 2 HCl  CaCl2 + H2O + Cl2
CaOCl2 + H2SO4  CaSO4 + H2O + Cl2
CaOCl2 + CO2  CaCO3 + Cl2
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 HNO3 is a strong oxidising acid to be avoided, here.

ESTIMATION OF AVAILABLE CHLORINE :

Let the wt. of sample of B.P. = W gm.

Add into a beaker containing acetic acid solution and excess K. A yellow brown solution is formed (3–)
2 + –  3–
Now few drops of starch solution is added into it. An intensive blue color is observed. Now hypo is used as the titrant. Note
the volume where the blue colour disappear.

 Reaction involved
CaOCl2 + 2CH3COOH  (CH3COO)2 Ca + H2O + Cl2
Cl2 + 2K  2KCl + 2
2 + 2S2O32–  S4O62– + 2–

Calculation :
1
[Mhypo  Vhypo ]   71
%Cl =
2  100
W
(vi) Bleaching powder converts acetone or ethyl alcohol into CHCl3
CaOCl2 + H2O  Ca(OH)2 + Cl2
CH3COCH3 + 3 Cl2  CCl3COCH3 + 3 HCl
2 CCl3COCH3 + Ca(OH)2  (CH3COO)2Ca + 2 CHCl3

 Some important order

(a) Acid strength :
(i) H > HBr > HCl > HF (ii) HOCl > HOBr > HO (iii) HClO4 > HClO3 >HClO2 > HClO

(b) Oxidising power :

(i) F2 > Cl2 > Br2 > 2 (According to electrode potential)

(ii) BrO4– > IO4– > ClO4– (iii) HClO4 < HClO3 < HClO2  HClO

(c) Order of disproportionation :

3 XO–  2X– + XO3– (hypohalite ion) ; O– > BrO– > ClO–
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PSEUDO HALOGENS & PSEUDO HALIDES:

Some inorganic compounds like (CN) 2 cyanogen, (SCN) 2 thiocyanogen, (SeCN) 2 selenocyanogen, (SCSN 3) 2
azidocarbondisulphide have been found to behave like halogens & they are known as pseudo halogen solids. Similarly few
ions are known, consisting of two or more atoms of which at least one is N, that have properties similar to those of the halide
ions. They are therefore called pseudohalide ions, e.g. (CN–) cyanide ion, (SCN–) thiocyanate ion, (SeCN–) selenocyanate
ion, (OCN–) cyanate ion, (NCN2–) cyanamide ion, (N3–) azide ion etc.
INTERHALOGEN COMPOUNDS :
We know that halogen atoms have different electronegativity. Due to this difference in electronegativity the halogen atoms
combine with each other and give rise to the formation of binary covalent compounds, which are called interhalogen
compounds.These are of four types.
AB AB3 AB5 AB7
ClF ClF3 ClF5 lF7
BrF BrF3 BrF5
ICl ICl3 IF5
IF IF3
PREPARATION:
(i) By the direct combination of halogens :
Cl2 + F2 (equal volumes)   2ClF ; Cl2 + 3F2 (excess) 
473 K
 2ClF3 ;
573 K

I2 + Cl2  2ICl ;

(equimolar)

 Diluted with water.

Br2 (g) + 3F2  2BrF3
 F2 is diluted with N2
78 º C
I2 + 3F2    2IF
3
 F2 is taken in freon.
Br2 + 5F2 (excess)  2BrF5
 IF7 can not be prepared by direct combination of I2 & F2 .

(ii) From lower interhalogens :

ClF + F  ClF ; ClF3 + F2 (excess)  
 ClF
350 º C
2 3 5

BrF3 + F2 (excess)    BrF ;IF + F   IF

200 º C 270 º C
5 5 2 7
 This method is generally applied for the preparation of halogen fluorides.
(iii) Other methods :
6HCl + KIO3 + 2KI  2KCl + 3H2O + 3ICl
250  350 º C
Cl2 + ClF3    3CIF ; KCl + 3F2    KF + ClF
200 º C
5

3l2 + 5AgF  5Agl + lF5 ; 8F2 + PbI2  PbF2 + 2lF7

PROPERTIES:
(i) These compounds may be gases, liquids or solids.
Gases : ClF, BrF, ClF3 , IF7 ; Liquids : BrF3, BrF5 ; Solids : ICl, IBr, IF3, ICl3.
(ii) Interhalogens containing fluorine are colourless but inter halogens consisting of heavier halogens are coloured. The intensity
of colour increases with increase in the molecular weight of the compounds.
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(iii) All interhalogens are covalent molecules and are diamagnetic in nature since all the valence electrons present as bonding or
non-bonding electrons are paired.
(iv) The boiling points increases with the increase in the electronegativity difference between A and B atoms.
(v) Thermal stability of AB type interhalogen compounds decreases with the decrease in electronegativity difference between A
and B atoms. IF > BrF > ClF > ICl > IBr > BrCl.
 More polar is the A – B bond more is the stability of interhalogen.
(vi) Interhalogen compounds are more reactive than the parent halogens but less reactive than F2.
ICl + 2Na  NaI + NaCl
The order of reactivity of some interhalogens is as follows :
ClF3 > BrF3 > IF7 > BrF5 > BrF.
(vii) Hydrolysis : All these undergo hydrolysis giving halide ion derived from the smaller halogen and a hypohalite (when AB),
halite (when AB3), halate (when AB5), and perhalate (when AB7) anion derived from the larger halogen.
AB + H2O  HB + HOA
BrCl + H2O  HCl + HOBr ; ICl + H2O  HCl + HIO2
ICl3 + 2H2O  3HCl + HIO2 ; IF5 + 3H2O  5HF + HIO2
IF7 + 6H2O  7HF + H5IO6 ; BrF5 + 3H2O  5HF + HBrO2

 Hydrolysis products are halogen acid and oxy-halogen acid. Oxy-halogen acid is of larger central halogen atom.

 Oxidation state of A atom does not change during hydrolysis.

(viii) Reaction with non-metallic and metallic oxides :
4BrF + 3SiO  3SiF + 2Br + 3O ;
3 2 4 2 2
4BrF3 + 3WO3  2WF6 + 2Br2 + 3O2
(ix) Addition reaction (of AB type compounds) :
– CH = CH – + ICI  – CHI – CHCl – ; CH2 = CH2 + BrCI  CH2Br – CH2Cl
(x) Reaction with alkali metal halides :
IBr + NaBr  NaIBr2 ; ICl3 + KCl  KICl4
Uses : These compounds can be used as non aqueous solvents. Interhalogen compounds are very useful fluorinating agents.
ClF3 and BrF3 are used for the production of UF6 in the enrichment of 235U .
U(s) + 3 ClF3 (l)  UF6 (g) + 3 ClF (g)

(F)GROUP 18 ELEMENTS : (THE ZERO GROUP FAMILY)

Group 18 Consists of six elements: helium, neon, argon, krypton , xenon and radon . All these are gases and chemically
unreactive. They form very few compounds . Because of this they are termed noble gases.
Occurrence :
All the noble gases except radon occur in the atmosphere. Their atmospheric abundabce in dry air is ~ 1% by volume of
which argon is the major constituent. Helium and sometimes neon are found in minerals of radioactive origin e.g., pitch-
blende, monazite, cleveite. The main commercial source of helium is natural gas. Xenon and radon are the rarest elements of
the group. Radon is obtained as a decay product of 226Ra.
88 Ra 86 Rn  2 He
226 222 4

 Most abundant element in air is Ar. Order of abundance in the air is Ar > Ne > Kr > He > Xe.
Electronic Configuration :
All noble gases have general electronic configuration ns2np6 except helium which has 1s2 . Many of the properties of noble
gases including their inactive nature are ascribed to their closed shell structures.
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Ionisation Enthalpy :
Due to stable electronic configuration these gases exhibit very high ionisation enthalpy . However, it decreases down the
group with increases in atomic size.
Atomic Radii :
Atomic radii increase down the group with increase in atomic number.
Electron Gain Enthalpy :
Since noble gases have stable electronic configurations, they have no tendency to accept the electron and therefore, have
larger positive values of electron gain enthalpy.

Physical properties :
All the noble gases are monoatomic. They are colourless, and tasteless. They are sparingly soluble in water. They have very
low melting and boiling points because the only type of interatomic interaction in these elements is weak dispersion forces,.
Helium has the lowest boiling point (4.2K) of any known substance. It has a unusual property of diffusing through most
commonly used laboratory materials such as rubber, glass or plastics.

ATOMIC & PHYSICAL PROPERTIES :

Element He Ne Ar Kr Xe
Atomic Number 2 10 18 36 54
Atomic Mass 4 20.18 39.10 83.80 131.30
2 6 2 6 10 2 6
Electronic configuration 1s 2
[He] 2s 2p [Ne] 3s 3p [Ar] 3d 4s 4p [Kr] 4d105s2 5p6
Atomic Radius (pm) 120 160 190 200 220
Ionization enthalpy / (kJ mol–1) 2372 2080 1520 1351 1170
Density (at STP)/g cm–3 1.8 × 10–4 9.0 × 10–4 1.8 × 10–3 3.7 × 10–3 5.9 × 10–3
Melting point / K – 24.6 83.8 115.9 161.3
Boiling point / K 4.2 27.1 87.2 119.7 165.0

Chemical Properties
In general, noble gases are least reactive. Their inertness to chemical reactivity is attributed to the following reasons:
(i) The noble gases expect helium (1S2) have completely filled ns2 np6 electronic configuration in their valence shell.
(ii) They have high ionisation enthalpy and more positive electron gain enthalpy.
The reactivity of noble gases has been investigated occasionally ever since their discovery, but all attempt to force them to
react to form the compounds were unsuccessful for quite a few years. In March 1962, Neil Bartlett, then at the University of
British Columbia, observed the reaction of a noble gas. First , he prepared a red compound which is formulated as O2+ PtF6–
. He , then realised that the first ionisation enthalpy of molecular oxygen (1175 kj mol –1) was almost identical with that
xenon (1170 kJ mol –1). He made efforts to prepare same type of compound with Xe+ PtF6 – by mixing Pt F6 and Xenon. After
this discovery, a number of xenon compounds mainly with most electronegative elements like fluorine and oxygen, have
been synthesised.
The compounds of krypton are fewer. Only the difluoride (KrF2) has been studied in detali. Compounds of radon have not
been isolated but only identified (e.g., RnF2) by radiotracer technique. No true compounds of Ar, Ne or He are yet known .
 If Helium is compressed and liquified it forms He() liquid at 4.2 K. This liquid is a normal liquid like any other liquid. But
if it is further cooled then He() is obtained at 2.2 K, which is known as super fluid, because it is a liquid with properties of
gases. It climbs through the walls of the container & comes out. It has very high thermal conductivity & very low viscosity.
Compounds of inert gases are of following two types.
(i) Physical compounds (possess no proper bonding)
Physical compounds may be (A) compounds whose existence is on the basis of spectroscopic studies (temporary phase not
isolated) and (B) clatherate compounds.
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Clatherate compounds :
Inert gas molecules get trapped in the cages formed by the crystal structure of water.
During the formation of ice Xe atoms will be trapped in the cavities (or cages) formed by the water molecules in the crystal
structure of ice. Compounds thus obtained are called clatherate compounds.
There are no chemical bonds. They do not possess an exact chemical formula but approx it is
6 water molecules : 1 inert gas molecule. The cavity size is just smaller than the atom of the noble gas. Such compounds are
also formed by the other organic liquids like dihydroxybenzene (for example quinol).
Xe, Kr or Rn (g)
(Not He or Ne)

H2 O
(cool)

(ii) True chemical compounds (posses proper bonding).

COMPOUNDS OF XENON :
(a) XENON DIFLUORIDE (XeF2):
PREPARATION:
873 K ,1 bar
(i) Xe + F2            XeF2
NiTube or monel metal (alloy of Ni)
 Volume ratio should be 2:1 otherwise other higher fluorides tend to form.
(ii)  C
Xe + O2 F2 118  XeF2 + O2
(iii) Xe + F2   XeF2
Hg ( arc )

(iv) Recently discovered method :

K+ [AgF4]– [potassium tetrafluoroargentate ()] is first prepared and this is reacted with BF3 .
BF3
K+ [AgF4]–  AgF3 (red solid) + KBF4
2 AgF3 + Xe  2 AgF2 (Brown solid) + XeF2
PROPERTIES:
(i) Colorless crystalline solid and sublimes at 298 K.
(ii) Dissolves in water to give a solution with a pungent odour. Much soluble in HF liquid.
(iii) This is stored in a vessel made up of monel metal which is a alloy of nickel.
(iv) Reaction with H2 : It reacts with hydrogen gas at 4000C
XeF2 + H2  Xe + 2HF
(v) Hydrolysis :

(a) 2XeF2 + 2H2O  2Xe + 4HF + O2 (slow)

The above is neither a cationic hydrolysis nor an anionic hydrolysis as seen in ionic equilibrium. It is a covalent compound
and hydrolysis is like that of PCl5 .

(b) Hydrolysis is more rapid with alkali.

1
XeF2 + 2 NaOH  Xe + O + 2NaF + H2O (fast)
2 2
The reaction (a) is slower probably due to dissolution of XeF2 in HF.
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(vi) Oxidising properties :

Higher the value of SRP better is the oxidising property of the species.
The standard reduction potential for XeF2 is measured to be + 2.64 V. Therfore it acts as a strong oxidising agent.
2e– + 2H+ + XeF2  Xe + 2HF; SRP = + 2.64 V
This oxidises halides to their respective halogens.
XeF2 + 2 HCl  Xe + 2 HF + Cl2

It oxidises 2Br –  Br2 + 2e– & 2–  2 + 2e–
 In this manner XeF2 will oxidise halide ions (except F–) into free halogens.
Similarly it can oxidise BrO3– (bromate) which are themselves good oxidising agents to BrO4– (perbromate ions) and Ce+3 to
Ce+4 ion.
(vii) Oxidising as well as fluorinating properties :
It can act as strong oxidising agent as well as fluorinating agent.
C6 H5  + XeF2  C6 H5 F2 + Xe ; CH3 + XeF2  CH3 F2 + Xe

 CH3 F2 exists as CH3+F2– ,F2– is analogous to 3–

F
–
:

: I hybridisation = sp3d
:

 F3– can not be formed as it has no d-orbitals to attain sp3d hybridisation.

(viii) Reactions of XeF2 + HF (anhydrous) :

Pt + 3XeF2 
 PtF + 3Xe ;
HF
6
S8 + 24 XeF2  8SF6 + 24 Xe

2CrF2 + XeF2  2CrF3 + Xe ; 2MoO3 + 6XeF2  2MoF6 + 6Xe + 3O2

Mo (CO)6 + 3 XeF2  Mo F6 + 3 Xe + 6CO

+ XeF2 
 2
HF
2 + Xe

8 NH3 + 3 XeF2  N2 + 6 NH4 F + 3 Xe

2NO2 + XeF2  2 NO2 F + Xe

(nitronium fluoride)
(ix) Formation of addition compounds : XeF2 reacts with fluoride ion acceptors to form cataionic species and fluoride ion
donors to form fluoroanions.
XeF2 + PF5  [XeF]+ [PF6]–

F5 (lewis acid) + XeF2  [XeF]+ [F6]– ; 2SbF5 (lewis acid) + XeF2  [XeF]+ [SbF6]–
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 Similar behaviour is shown by PF5 and AsF5

Structure : Shape linear and geometry trigonal bipyramidal.

hybridisation = sp3d

(b) XENON TETRAFLUORIDE (XeF4) :

PREPARATION:
873 K,
Xe + 2F2  
 XeF4
7 bar ,
1 : 5 Nitube
PROPERTIES:
(i) It is a colorless crystalline solid and sublimes at 298 K.
(ii) It undergoes sublimation, soluble in CF 3 COOH. It undergoes hydrolysis violently hence no moisture
must be present during it’s preparation.
(iii) Reaction with H2O :
6 XeF4 + 12 H2O  4 Xe + 2XeO3 + 24 HF + 3O2

 XeO3 is white solid and explosive compound (dry), soluble in water (well behaved in water)
 XeO3 reacts with NaOH forming sodium xenate
XeO3 + NaOH  Na+ [HXeO4]– (sodium xenate)
 It disproportionates into perxenate ion in basic medium.
2 [HXeO4]– + 2OH–  [XeO 6] + Xe + O2 + 2H2O
4–

Xenic acid (H2XeO4) is a very weak acid.

(i) [XeO]64– H+ (ii) [XeO6]4– +Mn+2 –

MnO4 + XeO3
water XeO3 + O2
(slow decomposition)
[XeO6]4– is obtainable as Na4 XeO6 . 8H2O (sodium perxenate)
(iv) Oxidising properties of XeF4 :
XeF4 + 2 H2  Xe + 4 HF ; XeF4 + 2 Hg  Xe + 2HgF2
(v) Addition reactions : XeF4 reacts with fluoride ion acceptors to form cataionic species and fluoride ion donors to form
fluoroanions.
XeF4 + SbF5  [XeF3]+ [SbF6]–
(vi) Fluorinating angen :
XeF4 + Pt  PtF4 + Xe ; XeF4 + 4NO  Xe + 4NOF (nitrosyl Fluoride)
XeF4 + 4 NO2  Xe + 4 NO2 F (nitronium fluoride) ; XeF4 + 2C6 H6  C6H5F + 2HF + Xe
Structure : Shape square planar & geometry octahedral

hybridisation = sp3d2
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(c) XENON HEXAFLUORIDE (XeF6) :

PREPARATION:

(i) Xe  3F2    XeF6

573 K , 60 – 70 bar

1 : 20 Nitube

(ii) XeF4 + O2 F2  XeF6 + O2

PROPERTIES :
(i) Colourless crystalline solid and sublimes at 298 K.
(ii) It gives yellow liquid on melting where as other form white liquids on melting (a point of difference)
(iii) HF is a good solvent for all three fluorides.

(iv) Hydrolysis :
(a) Complete hydrolysis : XeF6 + 3H2 O  XeO3 (white solid) + 2HF

(b) Partial hydrolysis : XeF6 + H2O  XeOF4 (colorless solid) + 2HF
(v) Reaction with silica (SiO2) :
2XeF6 + SiO2  2XeOF4 + SiF4
(vi) Thermal decomposition (effect of heat) :

2XeF6  XeF2 + XeF4 + 3 F2

 XeF2 & XeF4 do not undergo decomposition

(vii) Formation of addition compounds :

XeF6 + SbF5  [XeF5]+ [SbF6]– ; XeF6 + BF3  [XeF5]+ [BF4]–

(viii) Reaction With H2 :

XeF6 + 3H2  6HF + Xe

(ix) Reaction of XeF6 with XeO3 :

XeO3 + 2 XeF6  3 XeOF4
(x) F– donating/ F– accepting properties :
XeF6 reacts with fluoride ion acceptors to form cataionic species and fluoride ion donors to form fluoroanions.
XeF6 + MF  M+ [XeF7]– (M = Na, K, Rb or Cs)

donation { XeF6 + PtF5  (XeF5+) (PtF6–)

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 Order of oxidising power :

XeF2 > XeF4 > XeF6

STRUCTURE : Shape caped octahedral (distorted oactahedral)

(d) XENON–OXYGEN COMPOUNDS :
Hydrolysis of XeF4 and XeF6 with water gives XeO3.

6 XeF4 + 12 H2O  4 Xe + 2 XeO3 + 24 HF + 3 O2

XeF6 + 3 H2O  XeO3 + 6 HF

Partial hydrolysis of XeF6 gives oxyfluorides, XeOF4 and XeO2F2 .

XeF6 + H2O  XeOF4 + 2 HF

XeF6 + 2 H2O  XeO2F2 + 4 HF

XeO3 is a colourless explosive solid and has a pyramidal molecular structure. XeOF4 is a colourless volatile liquid and has
a square pyramidal molecular structure.
Uses :
Helium is a non–inflammable and light gas. Hence, it is used in filling ballons for meterological observations. It is also used
in gas–cooled nuclear reactors. Liquid helium (b.p.4.2 K) finds use as cryogenic agent for carrying out various experiments
at low temperatures. It is used to produce and sustain powerful superconducting magnets which form an essential part of
modern NMR spectrometers and Magnetic Resonance Imaging (MRI) systems for clinical diagnosis. It is used as a diluent
for oxygen in modern diving apparatus because of its very low solubility in blood.
Neon is used in discharge tubes and fluorescent bulbs for advertisement display purposes. Neon bulbs are used in botanical
gardens and in green houses.
Argon is used mainly to provide an inert atmosphere in high temperature metallurgical process (arc welding of metals or
alloys) and for filling electric bulbs. It is also used in the laboratory for handing substances that are air–sensitive.
Xenon and Krypton are used in light bulbs designed for special purposes.