Question:medium

Given below are two statements regarding conformations of n-butane. Choose the correct option. 

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Anti-staggered conformations are always the most stable in alkanes.
Updated On: Feb 24, 2026
  • Both Statement I and Statement II are false
  • Statement I is false but Statement II is true
  • Statement I is true but Statement II is false
  • Both Statement I and Statement II are true
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The Correct Option is D

Solution and Explanation

To determine the correctness of the statements regarding the conformations of n-butane, we need to review their stability.

  1. Understanding Conformations of n-Butane:
    • n-Butane has several conformations due to the rotation around the C-C bond.
    • The major conformations are: fully eclipsed, gauche, and anti.
  2. Analyzing the Conformations:
    • Fully Eclipsed Conformation (X): This occurs when the two methyl groups (CH3) are directly aligned with each other. It is the least stable due to maximum steric hindrance.
    • Anti Conformation (Y): The methyl groups are positioned 180 degrees apart, minimizing repulsive interactions. It is the most stable conformation.
  3. Conclusion:
    • Statement I: "Fully eclipsed conformation is the least stable" is true.
    • Statement II: "Anti conformation is the most stable" is true.

Therefore, the correct answer is: Both Statement I and Statement II are true.

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