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Resonance stabilization in amines can affect their basicity. In aromatic amines, the lone pair of electrons on nitrogen is delocalized into the ring, reducing their ability to act as a base.
Updated On: May 5, 2026
  • Aliphatic amines are weaker bases than NH\(_3\) while aromatic amines are stronger bases than NH\(_3\).
  • Gabriel phthalimide synthesis is used for preparing both Ethyl amine and Aniline.
  • Anilinium ion is less resonance stabilized than Aniline.
  • Sec-butylamine is optically inactive because Nitrogen atom of the \( \text{–NH}_2 \) group is achiral.
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The Correct Option is C

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