QuestionElimination / E2 stereochemistry
Which isomer of 1,2,3,4,5,6-hexachlorocyclohexane shown below undergoes E2 elimination (dehydrohalogenation) most slowly?

- (a) Cl wedge/wedge/wedge/hash/wedge/hash around the ring
- (b) All six Cl on wedges (all-cis)
- (c) Cl alternating wedge/hash around the ring (all-trans, β-isomer)
- (d) Three adjacent Cl on wedges and three adjacent on hashes
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