Explain why 1-chlorobicyclol2.2.llheptane, even though it is a tertiary alkyl halide, is virtually unreactive in the S1

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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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Organic Chemistry

ISBN: 978-0981519432

5th edition

Authors: Marc Loudon

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Question Posted: Apr 26, 2016 08:53 AM

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Explain why 1-chlorobicyclol2.2.llheptane, even though it is a tertiary alkyl halide, is virtually unreactive in the S1

Question:

CI 1-chlorobicyclo 2.2.1heptane

Step by Step Answer:

If this compound were to undergo solvolysis it would have to form carbocation A As a model ...View the full answer

Organic Chemistry

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