[References) 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 H₂C H C6H5 Draw the E2 elimination product of the reaction. Take into account that the starting stereochemistry affects the resulting double bond stereochemistry. CeHs Br CHICH,O Na CH₂CH₂OH . 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. 2-81

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References)
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
H₂C
H
C6H5
Draw the E2 elimination product of the reaction. Take into account that the starting stereochemistry affects the resulting double bond stereochemistry.
CeHs
CHICH,O Na
CH₂CH₂OH
Br
. 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.
.24
۴ ] کر
Transcribed Image Text:References) 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 H₂C H C6H5 Draw the E2 elimination product of the reaction. Take into account that the starting stereochemistry affects the resulting double bond stereochemistry. CeHs CHICH,O Na CH₂CH₂OH Br . 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. .24 ۴ ] کر
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