Aniline (PhNH2) is significantly less basic than most amines. What is the reason for this? a. It does not have a lone pair to donate to the proton b. The lone pair is stabilized by electron delocalization c. The positive charge on the nitrogen repels protons d. The electron delocalization stabilizes the extra proton e. The phenyl group is electron-donating, making the nitrogen less basic

Aniline (PhNH2) is significantly less basic than most amines. What is the reason for this? a. It does not have a lone pair to donate to the proton b. The lone pair is stabilized by electron delocalization c. The positive charge on the nitrogen repels protons d. The electron delocalization stabilizes the extra proton e. The phenyl group is electron-donating, making the nitrogen less basic

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Question

Aniline (PhNH₂) is significantly less basic than most amines. What is the reason for this?

a. It does not have a lone pair to donate to the proton

b. The lone pair is stabilized by electron delocalization

c. The positive charge on the nitrogen repels protons

d. The electron delocalization stabilizes the extra proton

e. The phenyl group is electron-donating, making the nitrogen less basic

Definition Definition Organic compounds with a nitrogen atom having a lone pair of electrons on it. Amines are derived from ammonia (NH 3 ), wherein hydrogen atoms are substituted by an aryl or alkyl group.

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