The isomer of 1,2,3,4,5,6-hexachlorocyclohexane shown undergoes E2 elimination 7000 times more slowly than any of its steroisomers. Explain this observation.
The isomer of 1,2,3,4,5,6-hexachlorocyclohexane shown undergoes E2 elimination 7000 times more slowly than any of its steroisomers. Explain this observation.
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 48AP
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The isomer of 1,2,3,4,5,6-hexachlorocyclohexane shown undergoes E2 elimination 7000 times more slowly than any of its steroisomers. Explain this observation.
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