• alkylamine
• amine
• arylamine
• azo compound (R–N=N–R′)
• Curtius rearrangement
• Gabriel amine synthesis
• heterocyclic amine
• Hofmann elimination reaction
• Hofmann rearrangement
• imide (O=C–N–C=O)
• primary amine (RNH₂)
• quaternary ammonium salt
• reductive amination
• Sandmeyer reaction
• secondary amine (R₂NH)
• tertiary amine (R3N)

Summary of Reactions

• Synthesis of amines (Section 24.6)
• Reduction of nitriles

• Reduction of amides

• Reduction of nitrobenzenes

• S_N2 Alkylation of alkyl halides

• Gabriel amine synthesis

• Reduction of azides

• Reductive amination of aldehydes/ketones

• Hofmann rearrangement of amides

• Curtius rearrangement of acyl azides

• Reactions of amines
• Alkylation with alkyl halides; see reaction 1(d)
• Hofmann elimination (Section 24.7)

• Diazotization (Section 24.8)

• Reactions of arenediazonium salts (Section 24.8)
• Nucleophilic substitutions

• Diazonium coupling