Why is acetaldehyde more reactive than acetone towards nucleophilic addition reactions ?

Why are aldehydes more reavtice than ketones towards nucleophilic addition reactions ?

Assertion : Acetaldehyde is more reactive than acetone in nucleophilic addition reactions. Reason Two alkyl groups in acetone reduce the electrophilicity of the carbon.

Benzaldehyde is less reactive than acetaldehyde towards nucleophilic addition reactions. Justify.

Which gives nucleophilic addition reaction?

Statement -1: Acetophenone gives aldol condensation. Statement-2: Benzaldehyde is more reactive than acetaldehyde towards nucleophilic addition. Statement-3: Benzophenone has alpha -Hydrogens

Which one is most reactive towards nucleophilic addition reaction?

Identify the incorrect statement // statement : (i) Alkynes are more reactive than alkenes towards electrophilic addiction reaction (ii) Alkynes are less reactive than alkenes towards electrophilic addiction reaction (iii) Alkynes decolourise Br_(2) water (iv) Addition of HBr to alkenes in presence of peroxide proceeds via Markownikoff's rule

Would you expect benzaldehyde to be more reactive or less reactive in nucleophilic addition reactions than propanal? Explain your answer.

Why are alkenes more reactive than alkanes ?