Chemical Bonding and Molecular Structure
🟢 Lite — Quick Review (1h–1d)
Rapid summary for last-minute revision before your exam.
Chemical Bonding — Key Facts
Chemical bonds hold atoms together in compounds. The three primary bond types are ionic, covalent, and metallic. Bond formation releases energy (exothermic) — breaking bonds requires energy.
Ionic Bonding:
- Transfer of electrons from metal to non-metal
- Example: Na (1s²2s²2p⁶3s¹) → Na⁺ (2s²2p⁶) + e⁻
- Cl (1s²2s²2p⁶3s²3p⁵) + e⁻ → Cl⁻ (1s²2s²2p⁶3s²3p⁶)
- Ionic compounds: high melting/boiling point, conduct electricity in molten state, soluble in polar solvents
Covalent Bonding:
- Sharing of electron pairs between non-metals
- Single bond (σ): 2 electrons shared
- Double bond (σ + π): 4 electrons shared
- Triple bond (σ + 2π): 6 electrons shared
- Polar covalent: unequal sharing due to electronegativity difference
Electronegativity (Pauling Scale):
- F = 4.0 (most electronegative)
- Trend: increases across period, decreases down group
- Difference > 1.7: ionic bond
- Difference 0.4–1.7: polar covalent
- Difference < 0.4: non-polar covalent
⚡ ECAT Exam Tip: Use the Fajan rule — cations with high charge and small size cause distortion of the electron cloud (polarisation), making ionic compounds more covalent.
🟡 Standard — Regular Study (2d–2mo)
For students who want genuine understanding…
Lewis Structures (Electron Dot Structures):
Steps to draw Lewis structures:
- Count total valence electrons
- Identify central atom (usually least electronegative, can form multiple bonds)
- Connect atoms with single bonds
- Complete octets of outer atoms
- Use lone pairs on central atom to form double/triple bonds if needed
Examples:
CO₂ (Carbon dioxide):
- Total valence e⁻ = 4 + 6 + 6 = 16
- O=C=O (double bonds to satisfy carbon’s octet)
NH₃ (Ammonia):
- Total valence e⁻ = 5 + 3(1) = 8
- Central N with 3 bonding pairs and 1 lone pair
- Trigonal pyramidal geometry
VSEPR Theory (Valence Shell Electron Pair Repulsion):
| Steric Number | Electron Pair Geometry | Molecular Shape |
|---|---|---|
| 2 | Linear | Linear |
| 3 | Trigonal planar | Trigonal planar, bent |
| 4 | Tetrahedral | Tetrahedral, trigonal pyramidal, bent |
| 5 | Trigonal bipyramidal | See-saw, T-shaped, linear |
| 6 | Octahedral | Octahedral, square pyramidal, square planar |
Hybridisation:
| Hybridisation | Geometry | Bond Angle | Example |
|---|---|---|---|
| sp | Linear | 180° | BeCl₂, C₂H₂ |
| sp² | Trigonal planar | 120° | BF₃, C₂H₄ |
| sp³ | Tetrahedral | 109.5° | CH₄, NH₃ |
| sp³d | Trigonal bipyramidal | 90°, 120° | PCl₅ |
| sp³d² | Octahedral | 90° | SF₆ |
⚡ ECAT Exam Tip: For molecules with resonance (like O₃, NO₃⁻), all resonance structures are valid but the actual structure is a hybrid. Formal charge calculation: FC = Valence e⁻ - (Non-bonding e⁻ + ½ Bonding e⁻).
🔴 Extended — Deep Study (3mo+)
Comprehensive coverage for students on a longer study timeline.
Molecular Orbital Theory (MOT):
Antibonding orbitals have a node between nuclei (higher energy); bonding orbitals have no node (lower energy).
Bond Order: $$Bond\ Order = \frac{N_b - N_a}{2}$$
where N_b = electrons in bonding orbitals, N_a = electrons in antibonding orbitals.
MOT for O₂:
- σ1s, σ1s, σ2s, σ2s, σ2pz, π2px = π2py, π2px = π2py, σ*2pz
- Total 16 electrons
- Bond order = (10 - 6)/2 = 2
- O₂ is paramagnetic (2 unpaired electrons in π* orbitals)
Hydrogen Bonding:
A special dipole-dipole attraction when H is bonded to highly electronegative F, O, or N.
Conditions:
- H bonded to F, O, or N
- Electronegative atom with lone pair
- Partial positive H attracted to lone pair
Examples:
- Water (H₂O): explains high boiling point (100°C), ice being less dense than liquid water
- Ammonia (NH₃): boiling point -33°C (higher than PH₃ which has only van der Waals)
- HF: boiling point 19.5°C
- DNA double helix: A-T and G-C base pairing
Dipole Moment (μ):
$$\mu = q \times d$$
Unit: Debye (D); 1 D = 3.336 × 10⁻³⁰ C·m
For CO₂: linear, μ = 0 D (vectors cancel) For H₂O: bent, μ = 1.85 D (vectors don’t cancel)
Van der Waals Forces:
-
London dispersion forces: Instantaneous dipole-induced dipole (present in all molecules)
- Strength increases with molecular mass and surface area
- Only intermolecular force in non-polar molecules
-
Debye forces: Polar molecule induces dipole in non-polar molecule
-
Keesom forces: Dipole-dipole interactions (in polar molecules)
Solubility Rules:
“Like dissolves like” — polar solvents dissolve polar/ionic solutes; non-polar solvents dissolve non-polar solutes.
Lattice Energy (Born-Haber Cycle):
Lattice energy = energy released when gaseous ions form one mole of solid ionic compound.
$$U \propto \frac{Z^+ Z^-}{r_0}$$
where Z = ion charge, r₀ = internuclear distance.
⚡ ECAT 2024 Analysis: MOT questions on bond order and paramagnetism appear frequently. Fajan rule and dipole moment calculations are also tested. Remember: He₂ has bond order 0 (doesn’t exist); Ne₂ has bond order 4 but is very unstable.
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📐 Diagram Reference
Clear scientific diagram of Chemical Bonding and Molecular Structure with atom labels, molecular structure, reaction arrows, white background, color-coded bonds and groups, exam textbook style
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