The mechanism of Hoffmann bromamide degradation is shown below,
In this reaction of alkyl as well as aryl group can migrate to electron deficient nitrogen atom. This migration of alkyl group is taking place towards electron dificient N-atom.
JEE Main 2022 — Chemistry Organic Chemistry
Given below are two statements :
Statement - I : In Hofmann degradation reaction, the migration of only an alkyl group takes place from carbonyl carbon of the amide to the nitrogen atom.
Statement - II : The group is migrated in Hofmann degradation reaction to electron deficient atom.
In the light of the above statements, choose the most appropriate answer from the options given below
Held on 27 Jun 2022 · Verified 6 Jul 2026.
Both Statement I and Statement II are correct.
Both Statement I and Statement II are incorrect.
Statement I is correct but Statement II is incorrect.
Statement I is incorrect but Statement II is correct.
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The correct order of the rate of reaction of the following reactants with nucleophile by SN1 mechanism is: (Given : Structure I and II are rigid) 
Identify the incorrect statements.  Choose the correct answer from the options given below:
For the following Friedel Craft's alkylation reaction, which of the statements are correct?  A. Major product is n-propyl benzene. B. iso-propyl carbocation intermediate is also generated. C. Multiple substitution is inevitable. D. Introducing electron-donating substituent on benzene will not produce any alkyl benzene. Choose the correct answer from the options given below:
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Consider the following reactions sequence  When the product (P) is subjected to Carius analysis using $AgNO_3$, $1.0$ g of the product (P) will produce _______ g of the precipitate of AgBr. (Nearest Integer) (Given: molar mass in g mol$^{-1}$ C : 12, H : 1, O : 16, N : 14, Br : 80, Ag : 108)
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