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🧪 Chemistry  ·  Amines  ·  NEET & JEE

Tertiary amines with Hinsberg's reagent:

Answer: Do not react (no N-H bond).

  • A Do not react (no N-H bond)
  • B Form soluble salt
  • C Form insoluble precipitate
  • D Undergo oxidation

Correct answer: A. Do not react (no N-H bond)

Explanation: Tertiary amines have no N-H bond and so do not react with Hinsberg's reagent.

Why Aniline Is a Weaker Base Than MethylamineNCH₃lone pair fully availableMethylamineN donates electrons freely → STRONG baseNlone pair delocalised into ringAniline

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.

Read the full Amines notes →