Question Description
Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared according to the Class 12 exam syllabus. Information about Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? covers all topics & solutions for Class 12 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer?.

Solutions for Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 12. Download more important topics, notes, lectures and mock test series for Class 12 Exam by signing up for free.

Here you can find the meaning of Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer?, a detailed solution for Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? has been provided alongside types of Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Hofmann’s bromamide degradation is used to convert a primary amide into primary amine. The proposed mechanism of reaction are :Q.If a pure enantiomer of amide given below is usedWhat can be predicted regarding product?a)Product amine will have inverted configuration at α-carbonb)Racemic mixture of product amine will be formedc)Product amine has the same sign of specific rotation as of starting ad)Product amine has same configuration at α-carbon as of starting amideCorrect answer is option 'D'. Can you explain this answer? tests, examples and also practice Class 12 tests.