MCQEasyJEE 2023Aromatic Compounds & Benzene

JEE Chemistry 2023 Question with Solution

Given below are two statements, one is labelled as Assertion A and the other is labelled as Reason R

Assertion A: Benzene is more stable than hypothetical cyclohexatriene. Reason R: The delocalized π\pi-electron cloud is attracted strongly by nuclei of carbon atoms.

In the light of the above statements, choose the correct answer from the options given below:

  • A

    A is true but R is false

  • B

    A is false but R is true

  • C

    Both A and R are correct but R is NOT the correct explanation of A

  • D

    Both A and R are correct and R is the correct explanation of A

Answer

Correct answer:D

Step-by-step solution

Standard Method

Given: Assertion states that benzene is more stable than hypothetical cyclohexatriene. Reason states that the delocalized π\pi electron cloud is strongly attracted by the nuclei of carbon atoms.

Find: Which option correctly relates the assertion and reason.

Benzene is more stable than hypothetical cyclohexatriene because of resonance stabilization. The delocalization of π\pi electrons in benzene creates extra stability compared to isolated double bonds in cyclohexatriene.

The delocalized π\pi electron cloud in benzene forms a bonding molecular orbital, which is strongly attracted by the nuclei of the carbon atoms, resulting in additional stabilization.

Therefore, both Assertion and Reason are correct, and Reason is the correct explanation of Assertion. The correct option is D.

The solution's lists Correct Answer: (3), but the extracted solution concludes D. Since the solution is the primary source, D is taken as correct.

Conceptual Explanation

Given: Benzene and hypothetical cyclohexatriene are being compared on the basis of stability.

Find: Whether the stated reason explains the higher stability of benzene.

In benzene, the π\pi electrons are delocalized over the ring rather than being confined to three separate double bonds. This delocalization lowers the overall energy of the molecule and gives resonance stabilization.

Because this delocalized electron cloud is spread over the carbon framework, it experiences stabilizing attraction from the carbon nuclei throughout the ring. Hence the reason directly accounts for the unusual stability of benzene.

Therefore, both statements are true, and the reason correctly explains the assertion. The correct option is D.

Common mistakes

  • Assuming benzene behaves like an ordinary cyclohexatriene is incorrect because benzene has delocalized π\pi electrons and resonance stabilization. Compare it with an aromatic system, not with isolated double bonds only.

  • Marking option C by thinking the reason is only a restatement is wrong because the reason gives the basis of stabilization: attraction of the delocalized π\pi cloud to the carbon nuclei. It does explain the assertion.

  • Treating delocalization as electron repulsion only is misleading. Delocalization lowers the energy of the molecule through bonding stabilization, so focus on net stabilization rather than only electron-electron repulsion.

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