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Which mechanism hinders free rotation around carbon-carbon bonds in hindered biaryl molecules?

A)Steric hindrance between substituent groups
B)Resonance stabilization within the aryl rings
C)Inductive effects from electron-withdrawing groups
D)Hyperconjugation with adjacent sigma orbitals

💡 Explanation

When large substituent groups are positioned on the aryl rings, steric hindrance occurs because they physically clash when rotation is attempted, creating a high energy barrier. Therefore, free rotation is restricted, rather than resonance, induction, or hyperconjugation, which primarily affect electronic properties and have a smaller impact on rotational freedom.

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