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Aldehyde and ketone undergo nucleophilic...

Aldehyde and ketone undergo nucleophilic addition reaction because of polarity between `gtC=O` group . The reactivity of carbonyl groups toward nucleophile depends upon the nature of inductive effect of froup present at carbonyl carbon.
Which of the following is least reactive for nucleophilic addition reaction

A

`C_(6)H_(5)-overset(O)overset(||)(C)-C_(6)H_(5)`

B

`C_(6)H_(5)-overset(O)overset(||)(C)-CH_(3)`

C

`C_(6)H_(5)-overset(O)overset(||)(C)-H`

D

`CH_(3)-overset(O)overset(||)(C)-H`

Text Solution

Verified by Experts

The correct Answer is:
A

`A=F CH_(2)CHO,` electron withdrawing group increases group increases electrophilicity of carbon increasing reate of nucleophilic addition reaction while conjugation or electron donating group decreases electrophilicity.
`C_(6)H_(5)-overset(O)overset(||)(C)-C_(6)H_(5)`
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Aldehyde and ketone undergo nucleophilic addition reaction because of polarity between gtC=O group . The reactivity of carbonyl groups toward nucleophile depends upon the nature of inductive effect of froup present at carbonyl carbon. Which among the following is more reactive towards nucleophilic addition reaction

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Aldehyde and ketone undergo nucleophilic addition reaction because of polarity between gtC=O group . The reactivity of carbonyl groups toward nucleophile depends upon the nature of inductive effect of froup present at carbonyl carbon. Nucleophilic addition reaction over carbonyl compound is shown by :

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