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Electrochemistry

The document provides information about electrochemistry and electrochemical cells. It defines electrochemistry as the branch of chemistry dealing with the production of electricity from spontaneous chemical reactions. It explains that electrolytes are substances that dissociate into ions in aqueous solution during electrolysis. Redox reactions involve both oxidation and reduction occurring simultaneously. Electrochemical cells like galvanic/voltaic cells produce electrical energy from spontaneous redox reactions between two half-cells separated by a salt bridge.

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0% found this document useful (0 votes)
625 views12 pages

Electrochemistry

The document provides information about electrochemistry and electrochemical cells. It defines electrochemistry as the branch of chemistry dealing with the production of electricity from spontaneous chemical reactions. It explains that electrolytes are substances that dissociate into ions in aqueous solution during electrolysis. Redox reactions involve both oxidation and reduction occurring simultaneously. Electrochemical cells like galvanic/voltaic cells produce electrical energy from spontaneous redox reactions between two half-cells separated by a salt bridge.

Uploaded by

Hunter Dracolus
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Electro

Chemistry
Dl9TALN0-E
Prepared By Bharat
- Panchal Sir

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-
Bharat Panchal Sir .. .

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Dimmitt bharal pancha 192
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cahuf.mji sst.io'
Electro -

Chemistry
Electrochemistry is the branch of chemistry which
deals with the study of the production of electricity
from energy released during spontaneous chemical
reactions .

ELECTROLYTE
Those substance which dissociate into
ions in their
aqueous solution on
passing electricity
Anode
millime cathode are called electrolyte $ this process

I
" ' c- '
is known as electrolysis .

'
- - - - t t.
weak electrolyte strong electrolyte
-

I*Ea÷ which dissociate partially which


dissociatempiefe.ly
e.g H
coz , CHS OH HCN,
, ,
e.g NaCl HCl NaOH
Mgcl, etc ,
,
.

etc
.

DEGREE OF IONISATION :
It is the ratio of number of ions

produced to the total number of


molecules in electrolyte .

REDOX REACTION :
a chemical reaction in which reduction
(
gain geo ? $ oxidation close of eo ) both takes
place simultaneously is called Redox Reaction

(E"
smallest device which is used to convert
one form of energy into another form of energy
as a result
of redox reaction
ELECTROCHEMICAL CELL electrical
"
heenheicagly
'
-

energy
ELECTROLYTIC Ceu :
electrical chemical

energy energy
-

GALVANIC CELL OR VOLTAIC CELL OR DANIELL CELL


when cell is designed in such a manner to make
the use
of spontaneous reaction between 2n and
cu ion to produce an electrical current .

L O A N
Tricks# . . .

¥¥o÷i¥iiim
'

cell Representation Negative


charge
¥'
oxidation 11 Reduction

Two Half Rxn are :

oxidation half Rxn →zn → znft + Leo


Reduction half RM
Fuat → + Leo Cu .

SALT BRIDGE It is an inverted U shaped


-

glass tube
which is filled with a

paste of Kd / kN 031 Kas op


in agar agar
-
whose one

end is dipped in one

beaker and second end


is dipped in another
beaker

FUNCTION :

It is used to complete the inner cell circuit

To maintain the electrical neutrality
°
To prevent the passage of one electrolyte into another

It is used to connect both the beakers .
Special case of DANIELL CELL :

cis Cii ) ( iii )

the
tendency
shows
ELECTRODE POTENTIAL : It

of an electrode
to either lose or
gain e
-
when it is placed
in its own solution .

STANDARD ELECTRODE POTENTIAL :


Electrode potential
of electrode at 250C I bar pressure
any ,
and IM solution is called standard
electrode potential And it is measured S Hot C
by
. -

standard
Hydrogen Electrode )

5. H E
-
or Nrm E .
: It is device which is used
the
to eattculale standard electrode
potential of any electrode .

Ha gas at 298 K temp .

and I atm .
pressure be passed
into IM Hee solution in which
with
a
platinum foil coated
platinum black remains immer .

- sed .

Through which inflow


and out
flow of eo takes place . So it can

act as oxidation as well as seduction


potential .

Oxidation at anode : Reduction at cathode :

Ha → 2 Htt Leo 2 Ht + geo - the


standard electrode potential of Hydrogen is zero .

Acc .
to IUPAC, stand .
red pot . . is standard electrode pot
DIFFERENCE BETWEEN ELECTROCHEMICAL AND

ELECTROLYTIC CELL

ELECTROCHEMICAL ELECTROLYTIC

Electrochemical series : -

Arrangement of various electrodes


in the
Li → -
3. osu
increasing order of their
K → -
2. a3v Inc .
standard reduction potential .

Ca → -2.87W Order chat chant def


Na -7 -
2.71 U of Trick mists
dik

3HfayT with
Standard
Mg → - 2.36 u Don 't
cry unit attract civil
Ae → - 1.66 U Red " both E cute.

In -7 -
076 U e, HIT 3isf-iioiglkd.se# at
'

Cr -7 -
0.74W rust

Fe → -
0.44 V Applications -

Ni -7 OLS v
-

dec - -

comparing
.

reducing
-

cis In relative
Sh → Olov order
0%34
-

and
Pb → oxidsing power of element
of standard Cii,
.
-

H -70.0011
to -3kV
predicting the feasibility
fu → oxi .

of a Redox Reaction .

I to -5kV

potential Chi , calculation of Eocell
Ag
.
.

→ to.gov
Bretton Civ ) comparison reactivity
"

SOV
of
Au → +l -

metals metals
F → + 2- 87 V Cf or non .
# E'
cell
= E'
red
-
Eooxi calculate Eceee of
=
E' - ⇐ 2h12 neat 11 Cut Icu
cathode Anode
Eeeeee -
Fred -

Toti
ER
=
-
Eh
= 034 - C -
0.76 )
= l -
10 V

NERNST EQUATION
.

IF the conc .

of species in the electrode


reaction is not equal to 1 then Nernst
, we use eqn .

e-
g
Mhteaq , Mcs )
0 →
the
.

Nernst e9 "
Ecmnym , Raff l"
{M#n+cag?
.

Ecmnym,
= -

E. → standard electrode potential


Rs Gas constant C 8.314 J ktm.tl )

T Tents 298K
'm

0.4592 leg[ Mn 'T



E
I n Em
.
-
=

>
of e
nolose
. or
gain -0

FT Faraday constant

for the cell -

neo
AA + BB
> mmmm
At 298k "
Einen Eeceee ( MIM ENT
00h51 log
.
-

EAT 9 [ B) a
Eee eee O
.05 log
=
tox
-

Red .

GIBBS ENERGY :
ago . -

nfeoeeee AU = -

hftcele
-
-

standard Gibbs ← leap Gibbs tree


free energy energy .

AT EQUILIBRIUM !

they =

00h54 log Kc

Kc →
equilibrium constant .
RESISTANCE :

every substance offers restrictions to the


flow of electricity to a small or large extent
5. I Unite =D (Ohm )

The electrical resistantonce of any object is


directly proportional to its length .

Ral
to its

Inversely proportional area


of Crosse ctia

Rx I i. e
A
is resistivity
Raha # where I
or R =p
specific resistance
or

SI unit is Ohm metre


CONDUCTANCE
The each with which current flows
conductance
through
is
a
iveose
conductor is known
resistance
as .
It

of
G-
Ip =

say =
Kay
where k is
conductivity
Cell constant !
The
quantity Gais called cell constant .

't
given by G
get I K 't
axe
-

= -

CONDUCTIVITY '
.

It is the reciprocal of resistivity and


denoted by Ki
k =
ax e-
A
electronic Ionic Molar conductance :

gym § conducting
power of all the ions
produced by one mole of
electrolyte in a solution .

It is denoted Am
by .

Mm - K X l ooo
-

M
S Cmb
Mol -
I
Am It always decreases with decrease in concentration
for weak and strong electrolyte .

1A Molar conductance increases with decrease in conc .

( or increase in dilution )

LIMITING MOLAR CONDUCTIVITY when C -70


,

Am = Ani i -
e

when concentration approaches zero ,


the molar
conductivity reaches limiting a value known as
molar conductivity
limiting .

Variation of nm with

( weak concentration is different


electrolyte ) for
strong and
weak
electrolyte .

( strong DEBYE -
HUCK EL RULE
electrolyte )
Ame Ani - AIT
And →
limiting molar and .

Am -7 molar conductivity
At constant c → cone .

shown
Dom KOHL RAUSCH 'S LAW .

This law States that


limiting
conductivity
molas
of electrolyte represented
an can be as

the sum of individual contributions of anion


and cation of the electrolyte .

Ain ( Hz COOH =
din CH COO
,
-

t din Ht

Application Cil The molar conductivity of weak electrolyte


at
infinite dilution can be calculated by
using Kohl rausch law
Aim
.

→ at concentration
l" ) Degree of dissociation Cy ) =

nom → at infinite
dilution
His Dissociation constant CK ) =
concentration
1- a
'

am Faraday 's first Law of Electrolysis


The amount

of substance deposited or liberated


at the electrodes is proportional
to the amount of electricity
passed through the electrolyte
w d Q w> amt .

of
sub
deposited
w
29
.

liberated or
w ZXIXT 27 electrochemical
-
-

E- Current equivalent
t -
-

time
Z= wt substance
eq .
.

of
96500

Aw Faraday 's second law of Electrolysis


when the
same amount do electricity passed
through two different
electrolyte connected in series than the
,
amount
of
substance deposited or liberated at the electrodes
is proportional to their equivalent weight .

Mass of Ag deposit = eq wt .
.

of Ag
Mass
of Ca deposit eq wt
.

of Cu .

Q. How
charge is required
much
for the reduction of I mot
of
't
zn to 2n ?
Aus 2nd -1 + Leo → 2h

Charge required -
- hf
=
2×96500
Eu Products of Electrolysis
The products of electro lysi
depend upon the nature of electrolyte being electro lysed and
the nature of the electrodes .

Molten NaCl : NaCl → Nat t U


-

At cathode
-

Matteo → Na
At Anode Cl →
Iz Uz tee
-

fused Na Br Nabs → Nat t Bo -

At cathode → Nat + leo → Na


At Anode → By Iz Bre tee
-

TRICK
& H2O → H
,
+ Oz
at cathode at anode
I
t .
4
To get produce at To
get produce at
cathode : Anode :
① Reduction Pot of Hao 7 Red "
① oxi potential of Hao > oxi
-

bot .

do cations of G -
I
,
9-2 bot .

of fed, soy ; 5042 -

and a -13 Of periodic table


NOT £05
-

It etc
Eg Nat Kt , cast, Mg Aest .
,
, ,
So reduction at So oxidation of Hao
of Hao occur ,

cathode occur at cathode


means Hg at cathode

② Olli .
Potential of Hao
② Reduction pot .

of Hao < Red


< AT Br, I
.
-

etc
Potential do other cations
.

oxidation
C. than cations of G -
1,9-2,4-13 ) so of
these ions at
CULT Agt Aust Cda ; zag
e.g ,
,
, anode .

seduction doesnt
So of H2O
occur at cathode
P.Y.CL $ NCERT →

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