Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

MeCOCl

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MeCHO

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MeCOOMe

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MeCOOCOMe

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Solution

The correct option is A MeCOCl
-Cl has -I effect

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Q. The most susceptible to nucleophilic attack at the carbonyl group among the given compound is:

Among the compounds, the most susceptible to nucleophilic attack to carbonyl group is

Q. Among the given compounds, the compound which is most susceptible to a nucleophilic attack at the carbonyl group is :

The most characteristic reaction of aldehyde and ketones is nucleophilic addition to carbon oxygen double bond. Aldehyde and ketones are easily susceptible to nucleophilic addition because of structural features. The trigonal planar arrangement of groups around the carbonyl carbon atom means that the carbonyl carbon atom is relatively open to attack from above and below the plane of carbonyl group. The partial positive charge on the carbonyl atom means that it is especially susceptible to attack by a nucleophile

Aldehyde reacts with $2^{\circ}$ amines to form

Q. When a nucleophile attacks a carbonyl compound, the one which is most reactive towards the nucleophile is:

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Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

The correct option is A MeCOCl-Cl has -I effect

The correct option is A MeCOCl
-Cl has -I effect