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NEET2025Chemistry
Q.

The correct order of decreasing basic strength of the given amines is:

  1. A

    N-methylaniline > benzenamine > ethanamine > N-ethylethanamine

  2. B

    N-ethylethanamine > ethanamine > benzenamine > N-methylaniline

  3. C

    N-ethylethanamine > ethanamine > N-methylaniline > benzenamine

  4. D

    benzenamine > ethanamine > N-methylaniline > N-ethylethanamine

Solution

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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