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Treatment of the following stereoisomer of 1-bromo-1,2-diphenylpropane with sodium ethoxide in ethanol gives a single st
Posted: Thu Jun 30, 2022 6:23 pm
by answerhappygod
- Treatment Of The Following Stereoisomer Of 1 Bromo 1 2 Diphenylpropane With Sodium Ethoxide In Ethanol Gives A Single St 1 (60.51 KiB) Viewed 177 times
Treatment of the following stereoisomer of 1-bromo-1,2-diphenylpropane with sodium ethoxide in ethanol gives a single stereoisomer of 1,2-diphenylpropene. H 0 H3C C6H5 H C6H5 99-85 Br Draw the E2 elimination product of the reaction. Take into account that the starting stereochemistry affects the resulting double bond stereochemistry. H3C. CH3CH₂O Na+ • Consider E/Z stereochemistry of alkenes. Do not show stereochemistry in other cases. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3CH₂OH H Sn [F Previous