Question

Arrange the following carbonyl compound in increasing order of their nucleophilic addition reaction.
Benzaldehyde, p-tolualdehyde, p-nitrobenzaldehyde, acetophenone.

Answer 1

Nucleophilic addition reaction is an additional reaction where a chemical compound with an electrophilic double or triple bond reacts with a nucleophile such that the double or triple bond is broken. The group which increases electrophilicity of carbonyl carbon has greater reactivity towards nucleophilic addition reaction.

Complete step by step answer:
If an electron withdrawing group is attached to carbonyl carbon that increases the reactivity of that carbonyl compound towards nucleophilic addition reaction. While the electron donating group decreases electrophilicity of carbonyl carbon hence decreases reactivity.
${{ + I}}$ Effect (electron donating inductive effect) is more in ketone than in aldehyde. Hence ketone is less reactive towards nucleophilic addition reactions.
Let us see the structure of each compound given in the question
Benzaldehyde

p-tolualdehyde

p-nitrobenzaldehyde

Acetophenone

Hence out of Acetophenone (contains ketone functional group) is less reactive towards nucleophilic substitution reaction.
Among aldehydes, ${{ + I}}$ effect is more in p-tolualdehyde due to electron donating $\;C{H_3}$ group attached at para position to the carbonyl group. And lowest in p-nitrobenzaldehyde due to electron withdrawing $\;N{O_2}$ group.
Hence order of their reactivity towards nucleophilic addition reaction is p-nitrobenzaldehyde, Benzaldehyde, p-tolualdehyde, acetophenone.

Additional information:
There are different types of nucleophilic addition reaction
For example

1. When aldehyde and ketone undergo nucleophilic addition reaction with $HCN$ it produces cyanohydrin.
2. When aldehyde undergoes reaction with monohydric alcohols it forms hemiacetal.

Note: The nucleophilic addition reaction is initiated by addition of proton to the $\pi$ bond of the carbonyl group, forming a resonance stabilized carbocation. A molecule of alcohol bonds to the carbonyl carbon of this intermediate and forming a protonated alcohol.