Question: Explain why 1-chlorobicyclol2.2.llheptane, even though it is a tertiary alkyl halide, is virtually unreactive in the S1 reaction. (It has been estimated that it is
Explain why 1-chlorobicyclol2.2.llheptane, even though it is a tertiary alkyl halide, is virtually unreactive in the S"1 reaction. (It has been estimated that it is 10-13 times as reactive as tert-butyl chloride!).
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CI 1-chlorobicyclo 2.2.1heptane
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If this compound were to undergo solvolysis it would have to form carbocation A As a model ... View full answer
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