Standard difficulty · 20 questions · 40 marks
Show your working for Sections B and C. Answers are on the last page — try every question first!
Hydrocarbons · AW-11C-HYD-2026-V1 · For parents — fold back or tear off before handing the sheet to your child.
| Q | Answer | Working |
|---|---|---|
| 1 | (d) CnH2n+2 | — |
| 2 | (a) 1-bromobutane | anti-Markovnikov (peroxide effect) |
| 3 | (c) alkyne | CnH2n−2 |
| 4 | (c) ortho and para (activating) | it releases electrons into the ring |
| 5 | (a) Pyridine | pyridine: 6 π electrons, cyclic, planar and conjugated (4n + 2) |
| 6 | (d) ethene | acidic dehydration |
| 7 | (b) but-2-ene | each carbon of the C=C must carry two different groups |
| 8 | (c) A is true, but R is false. | A is true: the main product is 2-methylpropan-2-ol. R is false. |
| 9 | When HX adds to an unsymmetrical alkene, the negative part (X) goes to the carbon with fewer hydrogen atoms. CH3CH=CH2 + HBr → CH3CHBrCH3 (2-bromopropane). | — |
| 10 | CH4 + 2O2 → CO2 + 2H2O; 2 mol | balance C, then H, then O |
| 11 | Propanone and methanal: CH3COCH3 + HCHO | ozonolysis breaks the C=C into two C=O |
| 12 | ethanal and propanal | each C=C carbon becomes C=O |
| 13 | Bromination; bromobenzene; electrophile Br+ | electrophilic substitution |
| 14 | Ethane (catalytic hydrogenation) | — |
| 15 | 88 g CO2; 36 g H2O | C2H4 + 3O2 → 2CO2 + 2H2O; 1 mol of C2H4 |
| 16 | butane, pentane, hexane; three products form, and they are hard to separate | any two alkyl groups can join |
| 17 | From alkenes and alkynes by hydrogenation over Ni, Pt or Pd: CH2=CH2 + H2 → CH3CH3. From alkyl halides by the Wurtz reaction: 2CH3Br + 2Na → C2H6 + 2NaBr (dry ether). From carboxylic acid salts by decarboxylation with soda lime: CH3COONa + NaOH → CH4 + Na2CO3; or by Kolbe’s electrolysis. | — |
| 18 | (a) 2-methylbut-2-ene; (b) 2-bromo-2-methylbutane; (c) 2-bromo-3-methylbutane | join the carbonyl carbons with a double bond; Markovnikov without peroxide |
| 19 | (a) 2C3H6 + 9O2 → 6CO2 + 6H2O; (b) 360 g; (c) 330 g CO2, 135 g H2O; (d) 465 g on each side | 2.5 mol of C3H6 |
| 20 | (a) Treat benzene with C2H5Cl with anhydrous AlCl3; (b) Pass ethyne through a red-hot iron tube at 873 K; (c) Treat benzene with concentrated HNO3 and concentrated H2SO4 | electrophilic substitution for groups on the ring |