Chemistry-
General
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Question

In the Hofmann rearrangement an unsubstituted amide is treated with sodium hydroxide and bromine to give a primary amine that has one carbon lesser than starting amide.
General reaction :

Mechanism :

If the migrating group is chiral then its configuration is retained. Electron releasing effects in the migrating group increases reactivity of Hofmann rearrangement.

  1.    
  2.    
  3.    
  4. B & C both are correct    

The correct answer is:


    Hoffmann rearrangement is 100% intramolecular. one amide will give only one amine with Br2/OHQ

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    General reaction :

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