There are eight diastereomers of 1, 2, 3, 4, 5, 6-hexachlorocyclohexane. Draw each in its more stable
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There are eight diastereomers of 1, 2, 3, 4, 5, 6-hexachlorocyclohexane. Draw each in its more stable chair conformation. One isomer loses HCI in an E2 reaction nearly 1000 times more slowly than the others. Which isomer reacts so slowly, and why?
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I H I H I H G H H H I CI H H fot H H I H2H H H H je j H H CI 7 C...View the full answer
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