When ionic bromination of cyclohexene is carried out, the product is trans-1,2-dibromocyclohexane. Gas chromatographic analysis with a heated injection port can result in the elimination of
When ionic bromination of cyclohexene is carried out, the product is trans-1,2-dibromocyclohexane. Gas chromatographic analysis with a heated injection port can result in the elimination of
Chapter20: Nucleophilic Substitution Reactions: Competing Nucleophiles
Section: Chapter Questions
Problem 9Q
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When ionic bromination of cyclohexene is carried out, the product is trans-1,2-dibromocyclohexane. Gas
chromatographic analysis with a heated injection port can result in the elimination of Br2 from the dibromo product
to regenerate the starting alkene . Thus, the GC properties of both the starting material and the adduct are of
interest. Predict the relative retention times of cyclohexene and trans-1,2-dibromocyclohexane on a nonpolar
column.
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