Aromatic Amine Formation (Edexcel A Level Chemistry)

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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, downloadable IB Chemistry revision notes

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

    • The phenylammonium ions, C6H5NH3+, are deprotonated by the addition of excess sodium hydroxide solution, NaOH (aq)

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Sonny

Author: Sonny

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Sonny graduated from Imperial College London with a first-class degree in Biomedical Engineering. Turning from engineering to education, he has now been a science tutor working in the UK for several years. Sonny enjoys sharing his passion for science and producing engaging educational materials that help students reach their goals.