Q1. S: [Ne] 3s²3p⁴; Cr: [Ar] 4s¹3d⁵; Br⁻: [Ar] 4s²3d¹⁰4p⁶ = [Kr].
Q2. BF₃ trigonal planar 120°; H₂O bent ~104.5°; PCl₅ trigonal bipyramidal 120°/90°.
Q3. Hydrogen bonding.
Q4. H₂O sp³; NH₃ sp³; BeCl₂ sp; SF₆ sp³d²; C₂H₂ sp.
Q5. SO₂: bent (AX₂E), sp², polar; resonance between two S=O / S–O structures.
Q6. Propane (London only) < dimethyl ether (dipole) < ethanol (H-bond). Ranks: −42, −24, 78 °C.
Q7. NF₃ trigonal pyramidal; bond dipoles + lone pair give net dipole — polar (small dipole, but nonzero).
Q8. Orbitals are probability regions: s spherical, p dumbbell, d cloverleaf. Pauli: max 2 e⁻/orbital, opposite spins. Hund: fill degenerate orbitals singly first.
Q9. Across: Zeff ↑, radius ↓ → IE ↑. Down: shell number ↑ + shielding → IE ↓.
Q10. Network: very high m.p., hard, insulator (diamond). Molecular: low m.p., soft, weak London (I₂). Difference: covalent network throughout vs discrete molecules.
Q11. Water's polar H-bonding network solvates ions via ion–dipole forces.
Q12. Many tiny gecko foot setae produce huge cumulative London dispersion contact area.
Q13. XeF₄: square planar (AX₄E₂), sp³d²; nonpolar — symmetric, dipoles cancel.