Question

Why is the inverted stereoisomer often the more abundant enantiomer in SN1 reactions that produce unequal mixture of enantiomers

Why do the E2 reactions of the diastereomeric cyclohexyl bromides shown below give different number of products?

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    Why can’t methyl substrates undergo elimination to give alkenes?

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Answer 1

eliminah other) H) Gr Cant elimi nato can eliminate br