Nucleophilic addition reaction will be most favoured in:

C H_{3}

C H_{2}

C H_{2} C

C H_{3}

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{(C H_{3})}_{2} C

O

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C H_{3} C H_{2} C H O

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C H_{3} C H O

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Solution

The correct option is D $C H_{3} C H O$
1.Aldehydes are most favoured than ketones for Nucleophilic addition reaction. Because ketones has two $+ I$ groups which produces less positive charge on carbonyl carbon
Hence it may be C and D
2. Here comes steric hinderance and large chain, C has large chain more electron releasing and $+ I$ effect. So that D is most favored.

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Nucleophilic addition reaction will be most favoured in:

C H_{3} - O | | C - H (i); C H_{3} - O | | C - C H_{3} (i i); E t - O | | C - H (i i i)

C H_{3} - C H_{2} - C H_{2} - O | | C - H (i v); P h - O | | C - C H_{3} (v); P h - O | | C - P h (v i)

C H_{3} - O | | C I - C H_{3}

C H_{3} - O | | C I I - C l

C H_{3} - O | | C I I I - N H_{2}

C H_{3} - O | | C I V - O H

C H_{3} - O | | C - O V - O | | C - C H_{3}

$C H_{3} - C H_{2} - C H_{2} - C \equiv C H L i N H_{2} - --- \to A (C H_{3})_{2} S O_{4} - ------ \to B$

C H_{3} C O C H_{3}, C_{6} H_{5} C O C H_{3}, C H_{3} C H O

C I - C H_{2} - C O O H, F - C H_{2} - C O O H, C H_{3} - C O O H

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