C3: Aromatic Chemistry and Reaction Mechanisms
Benzene delocalisation stability, electrophilic aromatic substitution, nitration, Friedel-Crafts acylation, amines.
Benzene delocalisation stability, electrophilic aromatic substitution, nitration, Friedel-Crafts acylation, amines.
Question:
Outline the mechanism for electrophilic nitration of benzene to nitrobenzene.
Model Solution & Mark Scheme:
1. Generation: HNO₃ + 2H₂SO₄ → NO₂⁺ + 2HSO₄⁻ + H₃O⁺. 2. Attack: Benzene π-electrons attack NO₂⁺ forming arenium intermediate carbocation (horseshoe delocalised over 5 carbons). 3. Deprotonation: HSO₄⁻ removes H⁺ from sp³ carbon, restoring aromatic ring: Arenium + HSO₄⁻ → Nitrobenzene + H₂SO₄.
Q1: Why is phenol more reactive than benzene?
Answer: Lone pair on oxygen partially delocalises into benzene π-system, increasing electron density and activating ring toward electrophiles.
Q2: Order the basicity of phenylamine, ammonia, ethylamine.
Answer: Ethylamine > Ammonia > Phenylamine. Ethyl group is electron-donating (+I); phenylamine delocalises N lone pair into ring.