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In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.
Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.
Q. 
How the following transformation can be best brought about?
  • a)
    {(CH3)2CHO}3AI;H3O+
  • b)
    then NaBH4 followed by H3O+
  • c)
    H2/Ni; high p and T
  • d)
    N2H4/NaOH/Heat
Correct answer is option 'B'. Can you explain this answer?
Verified Answer
In general, ketones are less reactive than aldehydes in nucleophilic a...
Aldehyde being more reactive, protected first by acetal formation followed by reduction of ketone group.
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Read the passage given below and answer the following questions:Reductive alkylation is the term applied to the process of introducing alkyl groups into ammonia or a primary or secondary amine by means of an aldehyde or ketone in the presence of a reducing agent. The present discussion is limited to those reductive alkylations in which the reducing agent is hydrogen and a catalyst or "nascent" hydrogen, usually from a metalacid combination; most of these reductive alkylations have been carried out with hydrogen and a catalyst. The principal variation excluded is that in which the reducing agent is formic acid or one of its derivatives; this modification is known as the Leuckart reaction. The process of reductive alkylation of ammonia consists in the addition of ammonia to a carbonyl compound and reduction of the addition compound or its dehydration product. The reaction usually is carried out in ethanol solution when the reduction is to be effected catalytically:Since the primary amine is formed in the presence of the aldehyde it may react in the same way as ammonia, yielding an additional compound, a Schiff's base (RCH= NCH2R) and finally, a secondary amine. Similarly, the primary amine may react with the imine, forming an addition product which also is reduced to a secondary amine Finally, the secondary amine may react with either the aldehyde or the imine to give products which are reduced to tertiary amines.Similar reactions may occur when the carbonyl compound employed is a ketone.Q. The reaction of ammonia and its derivatives with aldehydes is called

In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer?
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In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. 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 In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. 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 In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer?.
Solutions for In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. 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 In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer?, a detailed solution for In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer? has been provided alongside types of In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice In general, ketones are less reactive than aldehydes in nucleophilic addition reaction, for both steric and electronic reasons.Hence, if a keto-aldehyde is treated with nucleophilic reagent, reaction occur first at aldehyde group.Q.How the following transformation can be best brought about?a){(CH3)2CHO}3AI;H3O+b)then NaBH4followed by H3O+c)H2/Ni; high p and Td)N2H4/NaOH/HeatCorrect answer is option 'B'. Can you explain this answer? tests, examples and also practice Class 12 tests.
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