{"@context":"https://schema.org/","@type":"Quiz","name":"Quiz about Problem Solving","about":"Problem Solving","url":"https://infinitylearn.com/question-answer/which-of-the-following-amides-are-more-reactive-th-64a54d813a587ebfcf937a5b","educationalAlignment":[{"@type":"AlignmentObject","alignmentType":"educationalSubject","targetName":"Problem Solving"}],"hasPart":{"@type":"Question","typicalAgeRange":"7-18","educationalLevel":"intermediate","eduQuestionType":"Multiple choice","learningResourceType":"Practice problem","assesses":"Problem Solving","name":"Question about Problem Solving","comment":{"@type":"Comment","text":"Find and solve problems on Problem Solving."},"text":"

Which of the following amides are more reactive than benzamide  (C6H5CONH2) towards Hoffmann bromamide reaction?

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electron releasing group at aryl ring stabilizes the transition state and rate of reaction increases whereas electron withdrawing groups like -NO₂and -Cl destabilizes the transition state and hence rate of reaction decreases. Hence, option A and option B are more reactive.

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Which of the following amides are more reactive than benzamide (C6H5CONH2) towards Hoffmann bromamide reaction?

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Which of the following amides are more reactive than benzamide $(C_{6} H_{5} C O N H_{2})$ towards Hoffmann bromamide reaction?