Question:

Given below are two statements: one is labelled as Assertion A and, the other is labelled as Reason R.
Assertion A: [6] Annulene, [8] Annulene and cis-[10] Annulene, are respectively aromatic, not-aromatic and aromatic.
Reason R: Planarity is one, of the requirements of aromatic systems.
In the light of the above statements, choose the most appropriate answer from the options given below.

Updated On: Dec 31, 2025
  • Both A and R are correct and R is the correct explanation of A
  • Both A and R are correct but R is NOT the correct explanation of A.
  • A is correct but R is not correct.
  • A is not correct but R is correct.
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The Correct Option is D

Solution and Explanation

To determine the correct answer to the question, let's examine both the assertion and the reason provided:

Assertion A: [6] Annulene, [8] Annulene, and cis-[10] Annulene, are respectively aromatic, non-aromatic, and aromatic.

Reason R: Planarity is one of the requirements of aromatic systems. 

  1. Analyzing Assertion A:
    • [6] Annulene: This molecule is aromatic because it satisfies the Huckel's rule for aromaticity, which requires the molecule to have \(4n+2\) π electrons, where \(n\) is a non-negative integer. Here, for [6] annulene, \(n=1\) (as it has \(4(1)+2 = 6\) π electrons).
    • [8] Annulene: This molecule is non-aromatic. According to Huckel's rule, it would require 10 π electrons to be aromatic, but it only has 8, which does not satisfy the rule.
    • cis-[10] Annulene: This molecule is also non-aromatic because it cannot maintain planarity due to angle strain and steric hindrance. Although it has 10 π electrons, its inability to be planar disqualifies it as aromatic.
  2. Analyzing Reason R:

Planarity is indeed one of the critical requirements for a compound to exhibit aromaticity. Aromatic compounds must have a cyclic, continuous overlap of p orbitals, which is only possible if the molecule is planar.

  1. Conclusion: Since Assertion A is incorrect but Reason R is correct, the correct option is: A is not correct but R is correct.
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Concepts Used:

Aromatic hydrocarbon

Aromatic hydrocarbons, sometimes known as arenes, are aromatic organic molecules made up entirely of carbon and hydrogen. In aromatic compounds a benzene ring which is named after the simple aromatic chemical benzene, or a phenyl group when part of a larger structure, is the configuration of six carbon atoms.

Read More: Aromaticity

Reactions of Aromatic Hydrocarbons:

1. Aromatic Substitution Reactions

This reaction involves the replacement of one substituent on the ring of an aromatic hydrocarbon, commonly a hydrogen atom, by a different substituent group.

The common types of aromatic substitution reactions are:

  • Nucleophilic aromatic substitution reactions
  • Electrophilic aromatic substitution reactions
  • Radical nucleophilic aromatic substitution reactions

2. Coupling Reactions

In these types of reactions, the coupling of two fragments that have a radical nature is achieved with the help of a metal catalyst