Aromatic Amine Formation
- Phenylamine is an organic compound consisting of a benzene ring and an amine (NH2) functional group
- Phenylamine is sometimes known as aminobenzene and aniline
- Nitrobenzene, C6H5NO2, can be reduced to phenylamine, C6H5NH2, according to the following two-stage reaction:
The two-stage reduction reaction of nitrobenzene to phenylamine
Stage 1 - Reduction of nitrobenzene
- Nitrobenzene, C6H5NO2, is reacted with tin, Sn, and concentrated hydrochloric acid, HCl
- Tin and hydrochloric acid act as reducing agents
- The reaction mixture is heated under reflux in a boiling water bath
- The phenylammonium ions, C6H5NH3+, are protonated due to the acidic conditions
Stage 2 - Formation of phenylamine
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- The phenylammonium ions, C6H5NH3+, are deprotonated by the addition of excess sodium hydroxide solution, NaOH (aq)