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Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared
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the Class 12 exam syllabus. Information about Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,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 Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer?.
Solutions for Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 12.
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Here you can find the meaning of Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of
Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer?, a detailed solution for Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer? has been provided alongside types of Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer? theory, EduRev gives you an
ample number of questions to practice Consider the following reaction,Q.The correct deduction(s) regarding mechanism of the above reaction is/area)Reaction involves nucleophilic addition at carbonyl carbonb)Ketones are more reactive than aldehydec)If carbonyl carbon turns chiral, racemic mixture of products is formed provided no other chiral carbon is presentd)If the intermediate aluminium salt is hydrolysed with DCI-D2Odeuterated alcohol (R—OD) is formedCorrect answer is option 'A,C,D'. Can you explain this answer? tests, examples and also practice Class 12 tests.