1. Consider the compound shown below. Draw the (S,S) stereoisomer. On treatment with Na* Eto- in a polar aprotic solvent, a single alkene product is formed. Draw that product and show a complete mechanism for its formation, using curved arrows. Be sure to explicitly denote stereochemistry in both the product and the mechanism. [Ph = phenyl group] H3CO Ph H3C Br

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1. Consider the compound shown below. Draw the (S,S) stereoisomer. On treatment with Na* Eto-
in a polar aprotic solvent, a single alkene product is formed. Draw that product and show a
complete mechanism for its formation, using curved arrows. Be sure to explicitly denote
stereochemistry in both the product and the mechanism. [Ph = phenyl group]
H3CO Ph
H3C
Br
Transcribed Image Text:1. Consider the compound shown below. Draw the (S,S) stereoisomer. On treatment with Na* Eto- in a polar aprotic solvent, a single alkene product is formed. Draw that product and show a complete mechanism for its formation, using curved arrows. Be sure to explicitly denote stereochemistry in both the product and the mechanism. [Ph = phenyl group] H3CO Ph H3C Br
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they asked us about the stereochemistry for the product also. can you tell me? the product looks like planar now. shouldnt there be a wedge for Ch3? thanks!

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