Question
Treatment of the following stereoisomer of 1-bromo-1,2-diphenylpropane with sodium ethoxide in ethanol gives a single stereoisomer of 1,2-diphenylpropene. Draw the E2 elimination product of the
Treatment of the following stereoisomer of 1-bromo-1,2-diphenylpropane with sodium ethoxide in ethanol gives a single stereoisomer of 1,2-diphenylpropene.
Draw the E2 elimination product of the reaction. Take into account that the starting stereochemistry affects the resulting double bond stereochemistry.
C6H5 H H3C C6H5 Br CH3CH3O* Na+ CH3CHOH
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Organic Chemistry structure and function
Authors: K. Peter C. Vollhardt, Neil E. Schore
6th edition
142920494X, 978-1429204941
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