An Overview of The Properties of Elements in The Periodic Table The Key Atomic Properties
An Overview of The Properties of Elements in The Periodic Table The Key Atomic Properties
The electron configuration (nl#: spdf notation) gives the distribution of electrons in principal energy
levels and sublevels of an atom.
The principal quantum number n determines the energy and relative distance of orbitals from
the nucleus;
The quantum number l yields s, p, d, and f notations, which describes the shape of orbitals in
the sublevel;
The superscript (#) tells the number of electrons in the sublevels.
Electrons in inner levels or shells tend to shield outer electrons from the full nuclear charge, which is
reduced to effective nuclear charge (Zeff). Electrons that have a greater penetration shield others more
effectively. For example, electrons in level n = 1 shield those in level n = 2 very effectively, and
those in n = 1 and n = 2 shield electrons in level n = 3. Electrons at the same level, but in different
sublevels, also shield other electrons to some extent. The extent of penetration and shielding effect is
in the order: s > p > d > f.
The effective nuclear charge (Zeff) greatly influence atomic properties. In general,
Zeff increases significantly across a period (left-to-right)
Zeff increases slightly down a group.
Elements within the same group have the same number of electrons in their valence (outermost)
shells, and they have similar electron configurations. They exhibit similar chemical properties.
Elements within the same period have different number of electrons in their valence shells (the
number is increasing from left to right) and different valence shell electron configuration. Therefore,
elements in the same period are chemically different.
Atoms do not have specific outer boundary; their atomic size is based on atomic radius, which is
one-half the internuclear distance of two bonded identical atoms. Two factors that greatly influenced
atomic size are principal quantum number (n) of valence shell and the effective nuclear charge (Zeff).
Since principal quantum number n increases down a group and Zeff increase significantly across a
period, the following general trends in atomic size are observed:
Atomic size increases down a group because the principal quantum number increases;
Atomic size generally decreases across a period because Zeff increases.
Ionization energy (IE) is the energy needed to remove a valence electron from 1 mol of gaseous
atoms. The relative size of the IE influences the types of ions and bonds an atom forms: an element
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with a low IE is more likely to lose electrons and form cations, and one with a high IE is more likely
to gain electrons and form anions or share electrons in a covalent bond (exclude noble gases). Since
the IE of an elements is influenced by the Zeff of the atom, the following trends are observed in the
periodic table:
IE generally increases across a period: Zeff increases and valence shell electrons are held
more firmly;
IE decreases down a group: valence electrons are farther away from the nucleus and held less
firmly.
The trends in IE are opposite those in atomic size: it is easier to remove an electron (lower IE) from
a large atom than from a small one.
Electron affinity (EA) is the energy change when electrons are added to 1 mol of gaseous atoms.
Two factors influenced EA, the Zeff of the atom and electron-electron repulsions. The following
trends of EA are observed in the periodic table:
EA generally becomes more negative (increases) across a period (exclude noble gases): as
Zeff increases the added electron comes into a stronger nuclear attraction.
EA becomes less negative (decreases) down a group: nuclear attraction is less effective when
an electron is added to the valence shell of a large atom.
However, if the atomic size is very small electron-electron repulsions become quite large. Thus, EA
of elements in the second period (n = 2) are generally less negative (lower) than the same group
elements in the third period (n = 3). Nonmetals (except the noble gases), especially those in Group
7A (17) and 6A (16), generally have a high IE (more positive) and EA (more negative) and they gain
electron quite readily to become anions.
Electronegativity (EN) is the relative ability of a covalently bonded atom to attract shared
electrons. EN follows a trend that is opposite to that in atomic size and the same as that in IE.
EN generally increases across a period: higher Zeff and shorter distance from the nucleus
strengthen the attraction for the shared electron pair(s);
EN generally decreases down a group: greater distance from the nucleus weakens the
attraction for the shared electron pair(s).
The difference in electronegativity (EN) between bonded atoms influences the physical and
chemical behavior of the compound, as shown below:
Physical properties
EN Bond polarity Molecular polarity Intermolecular forces Solubility
Reactivity
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Types of Bonding: ionic, covalent, and metallic.
Ionic bond is the electrostatic attraction between cations and anions. The strength of ionic bond
increases as the ion’s charge becomes larger and ion’s size decreases. This type of bonding leads to
crystalline solids with ions packed tightly in regular lattice structures.
Covalent bond results from the attraction between two nuclei and a localized electron pair. The bond
arises through electron sharing between nonmetal atoms or between a semimetal and a nonmetal
atoms, which leads to discrete molecules with specific shapes or to extended networks.
Bond length and bond energy are related to extent of overlap of atomic orbitals. Among similar
compounds, they relate to reactivity. For example, C—X bond length in CX 4 molecules increases in
the order: C—F < C—Cl < C—Br < C—I.
The bond energy decreases in the order: C—F > C—Cl > C—Br > C—I .
The reactivity of the compounds increases in the order: CF4 < CCl4 < CBr4 < CI4. Thus,
As bond length increases, bond energy decreases: shorter bonds are stronger;
As bond energy decreases, reactivity increases: easier to break weaker bonds.
In a covalent bond, the shared electrons reside in the entire region of the overlapping orbitals of
bonded atoms. Orbitals overlap in two ways, which leads to two types of bonds:
End-to-end overlap (involving s, p, and hybrid atomic orbitals) leads to a sigma () bonds,
which has a symmetrical electron density distribution along the bond axis. A single bond is a
-bond.
Side-to-side overlap (involving two parallel p orbitals) leads to a pi () bond, which has
electron density distribution above and below the bond axis. A double bond consists of one
-bond and one -bond. A -bond restricts rotation around the bond axis, leading to different
spatial arrangements of the atoms in such molecules. In organic chemistry, -bonds are often
sites of reactivity.
Metallic bond results from the attraction between the cores of metal atoms (nuclei plus inner-shell
electrons) and their delocalized valence electrons. This bonding, which is called the “sea of
electrons” model, leads to crystalline solids (similar to ionic crystals) and accounts for the special
characteristics of metals, such as their lustrous appearance, conductivity, malleability, and ductility.
Most substances exhibit bonding characteirstics that lie between these distinct models. For
example, the electron density depictions show that electron clouds overlap slightly even in ionic
bonding (NaCl, KBr, etc.). They overlap significantly in polar covalent bonding (HCl, H 2O, etc.) and
completely in nonpolar covalent bonding (H2, Cl2, etc.).
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Some generalization:
For the following series of elements:
Na, Mg, Al, Si, P4, S8, and Cl2;
most most
metallic covalent
Metallic character increases from right to left; covalent character increases from left to right.
Ionic character increases from right to left; covalent character increases from left to right.
Ionic character increases from right to left; metallic character increases from left to right.
The ionic bond character increases as EN becomes greater.The polarity of covalent bonds
decreases as EN becomes smaller. Thus, compounds formed between metals of Group 1A(1) and
nonmetals of Group 7A(17) exhibit the most ionic character. Those made up of elements (nonmetals)
in Groups 6A(16) and 7A(17) are the most covalent and are nonpolar or least polar. Substances
made up of Groups 1A and 2A elements are mostly metallic.
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Molecular Shapes
The shape of a molecule is defined by the relative positions of the nuclei of the bonded
atoms.
According to the VSEPR theory for “simple” molecules, molecular shapes are determined by
the number of bond pairs and lone pairs and their geometrical orientation around the central
atom. The geometrical orientations of bond pairs around the central atom are as follows:
Chemical Properties Lose electrons to become cations Gain electrons to become anion
Reacts with nonmetals to form Reacts with metals to form
ionic compounds (salts) ionic compounds
Metals do not react with Nonmetals (except noble gases)
one another reacts to form covalent compds.
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General trends of metallic and nonmetallic behaviors of elements in the periodic table:
Metallic properties increase and nonmetallic properties decrease top to bottom within the
group;
Metallic properties decrease and nonmetallic increase left to right across periods;
Reactivity of metals in the main groups increases from top to bottom and decrease from left to
right across periods;
Reactivity of nonmetals (noble gases excluded) decreases top down within groups and
increases from left to right across period.
Oxidation-Reduction Properties
The relative ability of an element to lose or gain electrons when reacting with other elements
defines its oxidation-reduction (or redox) property. A redox reaction occurs if the oxidation number
(o.n.) of any atoms in the reactants are different from those in the products.
In a redox reaction, the reactant that gives up electrons is the reducing agents and those that
gain electrons are the oxidizing agents;
In redox reactions, reducing agents got oxidized and oxidizing agents got reduced;
Metals are generally reducing agents and nonmetals are oxidizing agents;
Reducing strength of metals increases from top to bottom down groups and decreases left to
right across periods;
Oxidizing strength of nonmetals (noble gases excluded) decreases from top to bottom down
groups and increases from left to right across periods;
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Oxidation Number (or State):
The oxidation number (or state) of atoms in free elements is zero;
In compounds, the oxidation state of fluorine is -1; the oxidation state of a Group 1A (1)
metal is +1, and the oxidation state of a Group 2A (2) metal is +2;
In compounds, the oxidation state of oxygen is -2; except in peroxides which is -1;
The oxidation state of hydrogen is +1 in compounds with nonmetals and -1 in hydrides of
metals;
When forming compounds with metals, the oxidation state of Cl, Br, and I is -1;
The highest oxidation state in a group equals the A-group number; for nonmetals the most
negative oxidation state equals to (A-group minus 8).
Nonmetals have more oxidation states than metals in the same group or period;
Generally, elements in odd-numbered groups have odd-numbered oxidation states and those
in even-numbered groups have even-numbered oxidation states that are stable;
Metals with more than one oxidation states exhibit more metallic behavior in their lower
oxidation states - they acts as a reducing agent;
An element with more than one oxidation state is a strong oxidizing agent when in its highest
oxidation state.
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different. Graphite is opaque, soft and flaky, while diamond in very hard and shiny. The
other nonmetals (N2, O2, F2, and Ne) are all gases.