acid hydrolysis of benzamide


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  • How is benzamide converted to benzoic acid?

    In the presence of an acid like dilute hydrochloric acid, the hydrolysis of benzamide with sodium hydroxide (NaOH) forms benzoic acid.
    Benzamide is first converted to sodium benzoate which is further acidified to benzoic acid.

  • If we protonate onto a lone pair with a strong acid, then the benzamide is acting as a base.
    However, a strong base can remove one of the hydrogen atoms on the nitrogen atom, resulting in an anion.
    Then the benzamide is acting as an acid.

  • Does benzamide on acidic hydrolysis gives benzoic acid?

    Hydrolysis with aqueous acid: This method involves heating benzamide with a strong acid like sulfuric acid (H₂SO₄) in water.
    The acidic environment promotes the cleavage of the amide bond, splitting the molecule into benzoic acid and ammonia (NH₃).

  • What is the reaction of acid hydrolysis?

    A hydrolysis reaction is a reaction in which one molecule breaks apart to form multiple smaller molecules.
    Acidic hydrolysis of an ester gives a carboxylic acid and an alcohol.
    Basic hydrolysis (saponification) of an ester gives a carboxylate salt and an alcohol.

  • The hydrolysis of an amide produces an organic acid and ammonia. Benzamide thus yields benzoic acid and ammonia.
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