Which of the following conformations will be the most stable?
General Organic Chemistry (GOC) · Class 11 · JEE Main Previous Year Question
Which of the following conformations will be the most stable?
- a✓
Conformation (a)
- b
Conformation (b)
- c
Conformation (c)
- d
Conformation (d)
Conformation (a)
Step 1: Identify the principle governing conformational stability For conformational stability in cyclic and acyclic systems:
- Staggered arrangements are more stable than eclipsed
- Bulky groups (like ) should be as far apart as possible
- The anti conformation (dihedral angle = 180°) is most stable for alkanes
Step 2: Analyze conformation (a)
Conformation (a) shows the structure where the two bulky methyl groups are in anti positions relative to each other — maximally separated (dihedral angle ≈ 180°). This minimizes steric interactions.
Answer: Option (a)
Key Points to Remember:
- Anti conformation: dihedral angle = 180°, most stable for n-butane
- Gauche conformation: dihedral angle = 60°, less stable
- Eclipsed conformation: dihedral angle = 0°, least stable
- Stability: anti > gauche > partially eclipsed > fully eclipsed
Practice this question with progress tracking
Want timed practice with adaptive difficulty? Solve this question (and hundreds more from General Organic Chemistry (GOC)) inside The Crucible, our adaptive practice platform.
More JEE Main General Organic Chemistry (GOC) PYQs
The incorrect statement regarding conformations of ethane is:
Staggered and eclipsed conformers of ethane are:
Consider the following compound (X): The most stable and least stable carbon radicals, respectively, produced by homolytic cleavage of corresponding C-H bond are:
Given below are two statements: Statement I: Hyperconjugation is not a permanent effect. Statement II: In general, greater the number of alkyl groups attached to a positively charged C-atom, greater…
The correct order of stability of following carbocations is: