The synthesis of carbohydrates can be particularly difficult because of the large number of chiral centers and OH functional groups present. Epoxides can be useful synthetic intermediates in carbohydrate synthesis. Draw the product of the reaction of a phenyl Gilman reagent with this epoxide.

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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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The synthesis of carbohydrates can be particularly difficult because of the large
number of chiral centers and OH functional groups present. Epoxides can be
useful synthetic intermediates in carbohydrate synthesis. Draw the product of
the reaction of a phenyl Gilman reagent with this epoxide.
A
• Use the wedge/hash bond tools to indicate stereochemistry where it
exists.
• Explicitly define the cis/trans stereochemistry of fused rings using
wedge or hash bonds.
• If enantiomers are formed, draw both.
• Separate multiple products using the + sign from the drop-down
menu.
Transcribed Image Text:The synthesis of carbohydrates can be particularly difficult because of the large number of chiral centers and OH functional groups present. Epoxides can be useful synthetic intermediates in carbohydrate synthesis. Draw the product of the reaction of a phenyl Gilman reagent with this epoxide. A • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Explicitly define the cis/trans stereochemistry of fused rings using wedge or hash bonds. • If enantiomers are formed, draw both. • Separate multiple products using the + sign from the drop-down menu.
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