The reaction of thiocyanogen (NPCS±SCPN) with cis-cyclooctene proceeds by anti addition. A bridged sulfonium ion is presumed

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The reaction of thiocyanogen (NPCS±SCPN) with cis-cyclooctene proceeds by anti addition.

A bridged sulfonium ion is presumed to be an intermediate. Write a stepwise mechanism for this reaction.

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Organic Chemistry

ISBN: 978-0072905014

4th edition

Authors: Francis A. Carey

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Question Posted: Apr 30, 2016 01:25 PM

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The reaction of thiocyanogen (N CS SC N) with cis-cyclooctene proceeds by anti addition.
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The reaction of thiocyanogen (NPCS±SCPN) with cis-cyclooctene proceeds by anti addition. A bridged sulfonium ion is presumed

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SCN NCSSCN

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The problem stipulates that a bridged sulfonium ion is an intermediate Therefore use t...View the full answer

Organic Chemistry

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