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Chemical Bonding

Ionic, covalent, coordinate bonds, VSEPR, hybridisation

Ionic BondCovalent BondVSEPR TheoryHybridisationMolecular Orbital TheoryHydrogen Bond
📋 PYQs Available:
20242023202220212020
Expert Content

Chemical Bonding and Molecular Structure

Why This Chapter Matters

Chemical bonding is tested in JEE every year — 6-10 marks. VSEPR theory, hybridisation, bond polarity, and molecular orbital theory are the main focus areas.

Core Concepts

1. Types of Bonds

Ionic: Metal + non-metal. Electron transfer. High mp/bp, conducts when dissolved.

Covalent: Non-metal + non-metal. Electron sharing. Lower mp/bp.

Coordinate/Dative: Both electrons from one atom (donor to acceptor). e.g., NH₃→BF₃

Metallic: Electron sea model. Good conductors.

Hydrogen bond: X-H···Y (X,Y = F,O,N). Explains high bp of water, HF.

2. VSEPR Theory

Electron pairs (bonding + lone pairs) repel → adopt geometry to minimise repulsion.

Lone pairs repel MORE than bonding pairs.

Electron pairsGeometryBond angle

|---|---|---|

2Linear180°
3Trigonal planar120°
4Tetrahedral109.5°
5Trigonal bipyramidal90°, 120°
6Octahedral90°

With lone pairs: geometry (name) of molecule changes but electron geometry stays.

H₂O: 4 pairs (2 bond + 2 lone) → bent, angle 104.5° (< 109.5° due to LP repulsion)

NH₃: 4 pairs (3 bond + 1 lone) → pyramidal, angle 107°

3. Hybridisation

sp: linear (BeCl₂, C₂H₂)

sp²: trigonal planar (BF₃, C₂H₄, benzene)

sp³: tetrahedral (CH₄, NH₃, H₂O)

sp³d: trigonal bipyramidal (PCl₅)

sp³d²: octahedral (SF₆)

Hybridisation = bond pairs + lone pairs on central atom (for valence shell)

4. Bond Parameters

Bond length: covalent radius sum. Inversely proportional to bond order.

Bond energy: energy to break one mole of bonds. Higher bond order → more energy needed.

Bond order = (bonding e⁻ - antibonding e⁻)/2

Triple bond > double bond > single bond (in terms of energy and strength)

5. Molecular Orbital Theory (MO Theory)

Atomic orbitals combine to form molecular orbitals.

σ and σ (antibonding, marked with )

Filling order: σ1s, σ1s, σ2s, σ2s, σ2p, π2p, π2p, σ2p

Bond order = (N_bonding - N_antibonding)/2

If BO > 0: stable molecule | BO = 0: molecule doesn't exist

O₂: BO = 2, paramagnetic (2 unpaired electrons in π*)

N₂: BO = 3 (most stable diatomic)

6. Polarity

Bond polarity: difference in electronegativity → dipole moment (μ = q × d)

Molecular polarity: vector sum of all bond dipoles.

CO₂: linear, dipoles cancel → non-polar

H₂O: bent → polar

CCl₄: tetrahedral, dipoles cancel → non-polar

CHCl₃: dipoles don't cancel → polar

PYQs

2024: Hybridisation and shape of XeF₄?

Xe: 8 valence e. 4 bonds (F) + 2 lone pairs = 6 pairs → sp³d² hybridisation.

4 bonding + 2 LP (opposite faces) → square planar geometry.

2023: Which has higher bond angle: H₂O or NH₃?

Both sp³-ish. NH₃ has 1 LP, H₂O has 2 LP.

More LP → more repulsion → more compression of bond angle.

NH₃: 107° > H₂O: 104.5°

2022: Bond order of O₂⁺, O₂, O₂⁻?

O₂ has 16 electrons. MO: BO of O₂ = 2. O₂⁺ (remove 1e from antibonding) BO=2.5. O₂⁻ (add 1e to antibonding) BO=1.5.

Revision Notes

VSEPR: electron pairs repel → min repulsion geometry
LP repel more than BP → angles compress

HYBRIDISATION:
sp: linear (2 pairs)
sp²: trigonal planar (3 pairs)
sp³: tetrahedral (4 pairs)
sp³d: trigonal bipyramidal (5 pairs)
sp³d²: octahedral (6 pairs)

COMMON SHAPES:
Linear: BeCl₂, CO₂, C₂H₂
Bent: H₂O (104.5°), SO₂
Pyramidal: NH₃ (107°), PCl₃
Tetrahedral: CH₄, CCl₄, SiCl₄
Square planar: XeF₄, [PtCl₄]²⁻

BOND ORDER = (bonding - antibonding)/2
Higher BO → shorter bond, more energy to break
O₂: BO=2, paramagnetic | N₂: BO=3
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