Answer: Tertiary.
- A Primary
- B Secondary
- C Tertiary
- D Aromatic
Correct answer: C. Tertiary
Explanation: Tertiary amines have three alkyl/aryl groups on nitrogen.
In aniline, the nitrogen's lone pair is pulled into the benzene ring through resonance, leaving less electron density available to accept a proton - which is why aniline is a much weaker base than methylamine, where the lone pair is fully available.
Concept context
Nitrogen-containing organic compounds. Covers classification (primary, secondary, tertiary), basicity comparison, preparation methods, and reactions including diazotization and coupling, key for understanding dyes and pharmaceuticals.