Cheat sheet · Class 12 · CBSE · Science Chemistry

Amines cheat sheet

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CBSE Class 12 · Chemistry

Cheat sheet

Chapter 9Amines

Hinsberg: 1° dissolves in alkali, 2° doesn't, 3° doesn't react.

1. Preparation

  • Reduction of nitro compounds, nitriles, amides.
  • Gabriel phthalimide: pure 1° amines (not aromatic).
  • Hoffmann bromamide: amide → amine with one less carbon.

2. Basicity

In water (aliphatic): 2° > 1° > 3° for methyl (ethyl: 2° > 3° > 1°). Aromatic amines are weaker bases (lone pair delocalised).

3. Tests & Reactions

Test / reactionObservation
Carbylamine (CHCl₃ + KOH)foul smell — 1° amines only
Hinsberg (C₆H₅SO₂Cl)distinguishes 1°, 2°, 3°
Nitrous acid with ArNH₂ (0–5 °C)diazonium salt
Bromination of aniline2,4,6-tribromoaniline (white ppt)

4. Diazonium Salts

  • Sandmeyer: –Cl, –Br, –CN.
  • Replacement by –I (KI), –F, –OH, –H.
  • Coupling with phenol/aniline: azo dyes.

5. Key Points

  • Acetylation tames aniline's reactivity.
  • Aniline gives meta product in strong acid (anilinium).
  • Amines have a fishy smell.
  • Diazonium salts are unstable above 5 °C.

Remember: Gabriel & Hoffmann | basicity order | carbylamine & Hinsberg

Amines: questions and notes

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