Consider the epoxidation of 1,2−dimethylcyclohexene with peroxybenzoic acid.In what positions will the methyl groups be in the epoxide?
A
Axial, equatorial
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B
Equatorial, equatorial
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C
Axial, axial
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D
None of these
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Solution
The correct option is D Axial, equatorial The epoxidation by peroxybenzoic acid always takes place in syn fashion that the epoxide formed by the reaction has methyl groups adjacent-axial-equatorial positions are cis to one another.