how will you achieve the synthesis of only 4 bromoaniline from aniline without production of trisubstituted aniline?
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Aniline reacts with Pyridine to give Phenylethanamide (CH3CO)2O. It further reacts with Bromine (Br2) in the presence of acetic acid (CH3COOH) to give Bromoacetanilide (it is the major product in the reaction). It can further react with either Hydogen ion or Hydroxyl ion to give Bromoaniline.
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How will you achieve the synthesis of only 4-bromoaniline from aniline without the production of the trisubstituted aniline.
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