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
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
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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help me pls
![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](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F56fab682-21f0-4c9e-87de-cdb34e61df22%2F2709030a-1919-4ccb-8488-3b16ad9890f8%2Fo8fczw_processed.png&w=3840&q=75)
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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