Comprehension Passage
Aldehydes are generally more reactive than ketones in nucleophilic addition reactions due to steric and electronic reasons. Sterically, the presence of two large groups in ketones hinders the attack of nucleophile to carbonyl carbon than in aldehydes. Electronically, aldehydes are more reactive than ketones because two alkyl groups reduce the electrophilicity of the carbonyl carbon more effectively than in the former.
The correct decreasing order of basic strength of following amines in aqueous solution is:
CH3NH2, (CH3)2NH, (CH3)3N, NH3
1
CH3NH2 > (CH3)2NH > NH3 > (CH3)3N
2
CH3NH2 > (CH3)2NH > (CH3)3N > NH3
3
NH3 > (CH3)3N > (CH3)2NH > CH3NH2
4
(CH3)2NH > CH3NH2 > (CH3)3N > NH3