The correct order of decreasing basic strength of the given amines is:
- A
N-methylaniline > benzenamine > ethanamine > N-ethylethanamine
- B
N-ethylethanamine > ethanamine > benzenamine > N-methylaniline
- C
N-ethylethanamine > ethanamine > N-methylaniline > benzenamine
- D
benzenamine > ethanamine > N-methylaniline > N-ethylethanamine
For aliphatic amines, more alkyl substitution increases electron density on N (in aqueous phase, with solvation, secondary > primary roughly): N-ethylethanamine (NH, secondary) > ethanamine (CHNH, primary).
Aromatic amines are weaker than aliphatic ones because the lone pair on N is delocalised into the ring. Among the two aromatic amines here, N-methylaniline has an extra +I methyl group on N, making it slightly more basic than benzenamine (aniline).
N-ethylethanamine > ethanamine > N-methylaniline > benzenamine.
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