Q1. (a) 3-methylpentane; (b) 2-methylbut-1-ene; (c) ethyl propanoate.
Q2. SO₃: trigonal planar; sp²; nonpolar (symmetric, dipoles cancel); resonance among three S=O / S–O structures.
Q3. ΔHf° = enthalpy change to form 1 mol of compound from its elements in standard states. Elements in standard state have ΔHf° = 0.
Q4. Kc = [NH₄⁺][OH⁻]/[NH₃]. Pairs: NH₃/NH₄⁺ and H₂O/OH⁻. Solution is basic (OH⁻ produced).
Q5. (a) +5; (b) +4; (c) +4; (d) +4.
Q6. Cl⁻: [Ar]; Fe³⁺: [Ar]3d⁵; Cu: [Ar]4s¹3d¹⁰; Mn: [Ar]4s²3d⁵.
Q7. (a) Amide; (b) Aldehyde; (c) Carboxylic acid; (d) Ether.
Q8. CH₂=CH₂ +H₂O/H⁺ → CH₃CH₂OH. CH₃CH₂OH +oxidation (PCC or limited K₂Cr₂O₇/H⁺) → CH₃CHO. CH₃CHO +KMnO₄ → CH₃COOH. CH₃COOH + CH₃CH₂OH /H₂SO₄ → CH₃COOCH₂CH₃ + H₂O (esterification).
Q9. [HI]₀=2.00. Let x = [H₂]=[I₂] formed; [HI]=2.00−2x. Kc = x²/(2.00−2x)² = 0.0185 → x/(2.00−2x) = 0.136 → x = 0.272 − 0.272x ⇒ x(1.272)=0.272 ⇒ x=0.214. So [H₂]=[I₂]=0.214 M; [HI]=2.00−0.428=1.57 M.
Q10. MnO₄⁻ + 8H⁺ + 5Fe²⁺ → Mn²⁺ + 5Fe³⁺ + 4H₂O. n(MnO₄⁻)=0.0250×0.01840=4.60×10⁻⁴; n(Fe²⁺)=5×4.60×10⁻⁴=2.30×10⁻³ mol. [Fe²⁺]=2.30×10⁻³/0.02500=0.0920 M; mass = 2.30×10⁻³ × 55.85 = 0.128 g.
Q11. ΔH = (−110.5) + (−283.0) = −393.5 kJ/mol.
Q12. x² ≈ Ka·C = 1.8×10⁻⁴ × 0.20 = 3.6×10⁻⁵ → x=6.00×10⁻³ → pH = 2.22.
Q13. CH₄: nonpolar, only London dispersion. NH₃: polar with H-bonding (one H-bond donor effective). H₂O: polar with two H-bond donors and two acceptors → strongest H-bonding network. B.p. order matches.
Q14. Curve: KE on x-axis, # molecules on y-axis; threshold Ea shown. ↑T: curve broadens / shifts right, more area beyond Ea. Catalyst: lowers Ea position to the left → more molecules exceed it. Both increase rate but via different mechanisms.
Q15. Initial pH ≈ 2.87. Half-eq (12.5 mL): pH = pKa = 4.74. Equivalence (25.0 mL): pH ≈ 8.7 (basic — acetate hydrolyzes). Indicator: phenolphthalein.
Q16. Anode (Zn|Zn²⁺) on left: Zn → Zn²⁺ + 2e⁻. Cathode (Cu²⁺|Cu) on right: Cu²⁺ + 2e⁻ → Cu. e⁻ flow Zn→Cu via wire; salt-bridge cations move to Cu side, anions to Zn side. E°cell = +1.10 V; net: Zn + Cu²⁺ → Zn²⁺ + Cu.
Q17. Addition: alkene → polyethylene; nonbiodegradable, persistent waste. Condensation: diacid+diol → polyester (or diamine+diacid → nylon); releases water; many polyesters are recyclable.
Q18. q = CΔT = 8.50 × 4.62 = 39.27 kJ. n(glucose)=0.500/180.16=2.775×10⁻³ mol → ΔHcomb = −39.27/2.775×10⁻³ = −14150 kJ/mol ≈ −14.2 MJ/mol. Per gram: 39.27/0.500 = 78.5 kJ/g (≈ 18.8 kcal/g) — close to the 4 kcal/g often cited (note: bomb calorimeter measures heat of complete oxidation; food values use Atwater factors).
Q19. ΔH<0 → ↓T favours forward (more NH₃). High kinetic barrier → ↑T needed for adequate rate. ↑P shifts forward (4 mol → 2 mol gas) and improves yield. Compromise: ~450 °C (rate good, eq still favourable enough), ~200 atm (yield + manageable equipment), Fe catalyst speeds attainment without shifting K.
Q20. Q = It = 1.50×10⁵ × 86 400 = 1.296×10¹⁰ C. n(e⁻) = 1.343×10⁵ mol → n(Al)=4.477×10⁴ mol → m = 4.477×10⁴ × 26.98 = 1.21×10⁶ g ≈ 1.21 t. Energy = QV = 1.296×10¹⁰ × 4.5 = 5.83×10¹⁰ J = 1.62×10⁴ kWh. Impacts: huge electricity demand (often coal/gas → CO₂); fluoride/perfluorocarbon emissions from cryolite bath.
Q21. C₆H₄(OH)COOH + (CH₃CO)₂O → C₆H₄(OCOCH₃)COOH + CH₃COOH. New ester (–OCOCH₃) replaces phenolic OH. Aspirin's ester hydrolyzes in moist air, releasing salicylic acid + acetic acid (vinegar smell).
Q22. (i) Ca²⁺/Mg²⁺ react with stearate to form insoluble scum, reducing surfactant action. (ii) Ca(OH)₂ + Mg²⁺ + HCO₃⁻ → CaCO₃(s) + Mg(OH)₂(s) (Ksp very low → ions removed); Na₂CO₃ + Ca²⁺ → CaCO₃(s). (iii) Mg²⁺ has smaller ionic radius → higher charge density → polarizes water more strongly → larger hydration enthalpy.