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Answer: 2. [structure shown in figure]

Key idea: a biphenyl is optically active (shows atropisomerism) only if rotation about the central bond is restricted and each ring lacks a plane of symmetry. This needs bulky groups at three or four ortho positions, with two different groups on each ring.

  • Option 1: no ortho groups, free rotation, not active.
  • Option 2: each ring has Br and I at the two ortho positions (2,2'-dibromo-6,6'-diiodo). Rotation is blocked and each ring is unsymmetric, so the molecule is chiral, optically active.
  • Option 3: only one ortho I per ring, rotation is not blocked enough.
  • Option 4: one ring has two identical ortho \(\mathrm{CH_3}\) groups and the other ring is unsubstituted, so it has a plane of symmetry.
Doubtly AI · 30 Oct 2026 AI-generated · not yet verified Report
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