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Ketone are less reactive than aldehydetowards nucleophilic addition. explain.?
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Ketone are less reactive than aldehydetowards nucleophilic addition. e...
In ketones alkyl groups are present at both sides hence steric hindrance increases.
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Ketone are less reactive than aldehydetowards nucleophilic addition. e...



Less Reactivity of Ketones compared to Aldehydes
Ketones are less reactive than aldehydes towards nucleophilic addition due to structural and electronic factors.

Electronic Factors
• The presence of an additional alkyl group attached to the carbonyl carbon in ketones decreases the electrophilicity of the carbon atom compared to aldehydes which have a hydrogen atom.
• The electron-donating alkyl groups in ketones stabilize the partially positive carbonyl carbon, reducing its reactivity towards nucleophilic attack.

Steric Factors
• The presence of two alkyl groups in ketones creates steric hindrance around the carbonyl carbon, making it more difficult for nucleophiles to approach and react with the carbon atom compared to aldehydes which have only one alkyl group.
• This steric hindrance reduces the likelihood of nucleophilic addition reactions in ketones.

Overall
In conclusion, the combination of electronic and steric factors in ketones makes them less reactive towards nucleophilic addition reactions compared to aldehydes. The presence of alkyl groups in ketones stabilizes the carbonyl carbon and creates steric hindrance, both contributing to the decreased reactivity of ketones in nucleophilic addition reactions.

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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

Ketone are less reactive than aldehydetowards nucleophilic addition. explain.?
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