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How can you convert an amide into an ami...

How can you convert an amide into an amine having one carbon atom less than the starting compound?

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By Hoffmann-bromamide reaction, i.e, by heating an amide with `Br_(2)` and KOH.
`underset("Amide")(RCONH_(2))+Br_(2) overset(Delta)toRNH_(2)+K_(2)CO_(3) + 2KBr + 2H_(2)O`
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The conversion of an amide into an amine with one carbon atom less by the action of alkaline hydrohalite is known as Hofmann bromamide rearrangement: RCONH_(2) overset(Br_(2)//KOH)toR-NH_(2) The most important feature of the reaction is the arrangement of N–bromamide anion to isocyanate : The product of the reaction Product amine will be :