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!).

Explain why 1-chlorobicyclol2.2.llheptane, even though it is a tertiary alkyl

CI 1-chlorobicyclo 2.2.1heptane

Step by Step Solution

3.37 Rating (156 Votes )

There are 3 Steps involved in it

1 Expert Approved Answer
Step: 1 Unlock

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

blur-text-image
Question Has Been Solved by an Expert!

Get step-by-step solutions from verified subject matter experts

Step: 2 Unlock
Step: 3 Unlock

Document Format (1 attachment)

Word file Icon

902-C-O-O-S (310).docx

120 KBs Word File

Students Have Also Explored These Related Organic Chemistry Questions!