MCQEasyJEE 2024Amines (Classification & Properties)

JEE Chemistry 2024 Question with Solution

Which of the following is strongest Bronsted base?

  • A

    Structure 1

  • B

    Structure 2

  • C

    Structure 3

  • D

    Structure 4

Answer

Correct answer:D

Step-by-step solution

Standard Method

Given: Four structures are compared for Brønsted basic strength.

Find: Which structure is the strongest Brønsted base.

A Brønsted base is a species that accepts a proton, H+\text{H}^+. The stronger base is the one whose lone pair is more readily available for protonation.

From the solution text:

  • Structure 1 is an aromatic amine, and the lone pair on nitrogen is involved in conjugation with the benzene ring, so it is less available.
  • Structure 2 has even greater resonance delocalization of the nitrogen lone pair through aromatic rings, so it is also weakly basic.
  • Structure 3 is more basic than the aromatic amines, but not as basic as a simple aliphatic amine.
  • Structure 4 is a simple cyclic amine with an sp3sp^3-hybridized nitrogen. Its lone pair is localized and readily available for protonation.

Therefore, Structure 4 has the greatest tendency to accept a proton.

The correct option is D.

Resonance vs lone-pair availability

Given: The options represent different nitrogen-containing structures.

Find: The structure with maximum proton-accepting tendency.

Basicity depends mainly on how available the lone pair on nitrogen is.

  • In aromatic amines, the lone pair can participate in resonance with the aromatic ring. This delocalization decreases its availability for bonding with H+\text{H}^+.
  • In a secondary aromatic amine attached to two phenyl rings, delocalization is even more significant, so the basicity decreases further.
  • A simple amine without such resonance has a more available lone pair and is therefore more basic.
  • A cyclic aliphatic amine with sp3sp^3 nitrogen has a localized lone pair and higher electron density on nitrogen, making protonation easier.

Hence the strongest Brønsted base among the given options is Structure 4, so the correct option is D.

Note: The actual structural diagrams are not present in the provided input, so the reasoning is taken directly from the provided solution text.

Common mistakes

  • Assuming all amines have nearly the same basic strength is incorrect because resonance can strongly reduce lone-pair availability. Always check whether the nitrogen lone pair is delocalized.

  • Choosing an aromatic amine as the strongest base is wrong when its lone pair participates in conjugation. A localized lone pair on an sp3sp^3 nitrogen is generally more available for protonation.

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