Chemical Bonding Short Notes by MTH

CHEMICAL BONDING
 The Electrovalency is the valency of the Element which is also equal to the number of unit charge on the
ion . e.g. calcium is assigned a positive electrovalence of two while the chlorine a negative electrovalence
of one .
 Formal Charge : It is the difference b/w no of valence electron of free atom and no of electron
assigned to it in Lewis Dot Structure.
F.C= Valence electron – (Lone pair) – ½( Bond Pair )
 Limitations of Octet Rule
The incomplete Octet of central atom

Examples are LiCl, BeH2, BCl3 Etc.
Odd Electron Molecules

In Molecule with an odd number of electrons like Nitric Oxide, NO and Nitrogen Dioxide , NO2,
the octet Rule is not Satisfied For all The Atoms .
E.g. NO, NO2.
The Expanded Octet

Elements in a and beyond the third period of the periodic table have part from 3s and 3p , 3d
orbitals also available for bonding . In a Number of Compounds of these Elements there are
more than eight valence electrons around the central atom. This is termed as the expanded
octet. Obviously, the octet rule does not apply in such cases.
Some of the examples of such compounds are: PF5, SF6, H2SO4 and a number of coordination
compounds
 Drawbacks of Octet Theory

Some noble gases (for example xenon and krypton) also combine with oxygen and fluorine to
form a number of compounds like XeF2, KrF2, XeOF2 etc.
 This theory does not account for the shape of molecules.
 It does not explain the relative stability of the molecules being totally silent about the energy of
a molecule.
IONIC OR ELECTROVALENT BOND
 Ionization is always an endothermic reaction.

 Electron affinity, is the negative of the energy change accompanying electron gain.
 ionic bonds will be formed more easily between elements with comparatively low ionization
enthalpies and elements with comparatively high negative value of electron gain enthalpy.
 The ammonium ion, NH4 + (made up of two non-metallic elements) is an exception. Generally
ionic bond is formed between METAL AND NON METAL
 IONIC BOND BETWEEN TWO METALS CsAu
 In ionic solids, the sum of the electron gain enthalpy and the ionization enthalpy may be positive
but still the crystal structure gets stabilized due to the energy released in the formation of the
crystal lattice. For example: the ionization enthalpy for Na+(g) formation from Na(g) is 495.8 kJ
mol–1 ; while the electron gain enthalpy for the change Cl(g) + e– → Cl– (g) is, – 348.7 kJ mol–1
only. The sum of the two, 147.1 kJ mol-1 is more than compensated for by the enthalpy of lattice
formation of NaCl(s) (–788 kJ mol–1). Therefore, the energy released in the processes is more
than the energy absorbed. Thus a qualitative measure of the stability of an ionic compound is
provided by its enthalpy of lattice formation and not simply by achieving octet of electrons
around the ionic species in gaseous state.
 The covalent radius is half of the distance between two similar atoms joined by a covalent bond
in the same molecule.

 The van der Waals radius represents the overall size of the atom which includes its valence shell
in a non-bonded situation.
 Van der Waals radius is half of the distance between two similar atoms in separate molecule in a
solid.
Bond Enthalpy:
It is defined as the amount of energy required to break one mole of bonds of a particular type
between two atoms in a gaseous state.
 It is important that larger the bond dissociation enthalpy, stronger will be the bond in the
molecule.
 Mean or average bond enthalpy : It is obtained by dividing total bond dissociation enthalpy by
the number of bonds broken.
Bond Order:
Bond Order is given by the number of bonds between the two atoms in a molecule. The bond order, for
example in H2 (with a single shared electron pair), in O2 (with two shared electron pairs) and in N2 (with
three shared electron pairs) is 1,2,3 respectively. Similarly in CO (three shared electron pairs between C
and O) the bond order is 3.
 Isoelectronic molecules and ions have identical bond orders; for example, F2 and O2 2– have
bond order 1.
 with increase in bond order, bond enthalpy increases and bond length decreases
Resonance:
 Resonance stabilizes the molecule as the energy of the resonance hybrid is less than the energy
of any single canonical( Normal )structure
 The cannonical forms have no real existence
 The molecule does not existfor a certain fraction of time in one cannonical form and for other
fractions of time in other cannonical forms.
 There is no such equilibrium between the cannonical forms as we have between tautomeric
forms (keto and enol) in tautomerism.
Polar and Non Polar Covalent Bond
When covalent bond is formed between two similar atoms, for example in H2, O2, Cl2, N2 or F2, the
shared pair of electrons is equally attracted by the two atoms. As a result electron pair is situated exactly
between the two identical nuclei. The bond so formed is called nonpolar covalent bond. Contrary to this
in case of a heteronuclear molecule like HF, the shared electron pair between the two atoms gets
displaced more towards fluorine since the electronegativity of fluorine is far greater than that of
hydrogen. The resultant covalent bond is a polar covalent bond
Dipole Moment :
As a result Of polarization , The Molecule Show Dipole Moment.
Dipole Moment = product of the magnitude of the charge and the distance between the centres of
positive and negative charge
Unit Conversion
1 Debye = 3.33564 × 10–30 C

 Peter Debye, the Dutch chemist received Nobel prize in 1936 for his work on X-ray
diffraction and dipole moments.
 The dipole moment in case of BeF2 is zero. This is because the two equal bond dipoles
point in opposite directions and cancel the effect of each other.
 In tetra-atomic molecule, for example in BF3, the dipole moment is zero although the B
– F bonds are oriented at an angle of 120o to one another, the three bond moments give
a net sum of zero as the resultant of any two is equal and opposite to the third.
Although fluorine is more electronegative than nitrogen, the resultant dipole moment of
NH3 (4.90 × 10–30 C m) is greater than that of NF3 (0.8 × 10–30 C m). This is because, in
case of NH3 the orbital dipole due to lone pair is in the same direction as the resultant
dipole moment of the N – H bonds, whereas in NF3 the orbital dipole is in the direction
opposite to the resultant dipole moment of the three N–F bonds.
 The smaller the size of cation and the larger the size of anion , the greater will be the
covalent character.
 Greater the charge on cation,the greater the covalent character of ionic bond
 The cation polarises the anion, pulling the electronic charge toward itself and thereby increasing
the electronic charge between the two. This is precisely what happens in a covalent bond, i.e.,
buildup of electron charge density between the nuclei. The polarising power of the cation, the
polarisability of the anion and the extent of distortion (polarisation) of anion are the factors,
which determine the per cent covalent character of the ionic bond.
 Lewis concept is unable to explain the shapes of molecules.

The main postulates of VSEPR theory are as follows:

 • The shape of a molecule depends upon the number of valence shell electron pairs (bonded or
nonbonded) around the central atom.
 • Pairs of electrons in the valence shell repel one another since their electron clouds are
negatively charged.
 • These pairs of electrons tend to occupy such positions in space that minimise repulsion and
thus maximise distance between them.
 • The valence shell is taken as a sphere with the electron pairs localising on the spherical surface
at maximum distance from one another.
 • A multiple bond is treated as if it is a single electron pair and the two or three electron pairs of
a multiple bond are treated as a single super pair.
 • Where two or more resonance structures can represent a molecule, the VSEPR model is
applicable to any such structure.
 While the lone pairs are localised on the central atom, each bonded pair is shared between two
atoms. As a result, the lone pair electrons in a molecule occupy more space as compared to the
bonding pairs of electrons.

Valance Bond Theory
 Valence bond theory was introduced by Heitler and London (1927) and developed further by
Pauling and others

When we study about a h2 atom when the both atoms approach to each other some amount of
energy is released in becoming stable and having a bond lenth 74pm which is Known as Bond
enthalpy.
 Attractive forces arise between: (i) nucleus of one atom and its own electron that is NA – eA and
NB– Eb
 (ii) nucleus of one atom and electron of other atom i.e., NA– eB, NB– eA.
 Similarly repulsive forces arise between
 (i) electrons of two atoms like eA – eB,
 (ii) nuclei of two atoms NA – NB.

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CHEMICAL BONDING

F.C= Valence electron – (Lone pair) – ½( Bond Pair )

 Limitations of Octet Rule

The incomplete Octet of central atom

Odd Electron Molecules

The Expanded Octet

 Drawbacks of Octet Theory

IONIC OR ELECTROVALENT BOND

 Ionization is always an endothermic reaction.

 IONIC BOND BETWEEN TWO METALS CsAu

Polar and Non Polar Covalent Bond

As a result Of polarization , The Molecule Show Dipole Moment.

1 Debye = 3.33564 × 10–30 C

The main postulates of VSEPR theory are as follows:

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