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Out of p-tolualdehyde and p-nitrobenzaldehyde ,which one is more reactive towards nucleophilic addition reactions, why?

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p-nitrobenzaldehyde is more reactive towards the nucleophilic addition reaction than ptolualdehyde as Nitro group is electron withdrawing in nature . Presence of nitro group decrease electron density, hence facilitates the attack of nucleophile . Presence of -CH3 leads to +I effect as - CH3 is electron releasing group.

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