Give reason why aldehydes and ketones undergo nucleophilic addition reaction
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In both aldehydes and ketones (carbonyl grop), C atom is double bonded with the O atom.
Since the electronegativity of O is more than the C atom, it pulls the shared pair of electron more towards itself.
Due to which C atom acquires partial +ve charge and O atom acquires partial -ve charge.
Hence nucleophile can easily attack on the C atom to neutralize the +ve charge and makes it stable.
Also pie bond (double bond) is being converted into a single bond (sigma), due to which it becomes more stable.
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