When benzaldehyde reacts with methyl B-D-glucopyranoside to form a six-membered cyclic acetal, a new chiral center is formed. Draw the structure of this product that has the (S) configuration at the new chiral center. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Use the "flat" representation of rings in your drawing. ChemDoodle" Submit Answer Try Another Version 2 item attempts remaining (Previous

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[References)
When benzaldehyde reacts with methyl B-D-glucopyranoside to form a six-membered cyclic acetal, a new chiral center is formed. Draw the
structure of this product that has the (S) configuration at the new chiral center.
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
• Use the "flat" representation of rings in your drawing.
ChemDoodle"
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Transcribed Image Text:[References) When benzaldehyde reacts with methyl B-D-glucopyranoside to form a six-membered cyclic acetal, a new chiral center is formed. Draw the structure of this product that has the (S) configuration at the new chiral center. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Use the "flat" representation of rings in your drawing. ChemDoodle" Submit Answer Try Another Version 2 item attempts remaining (Previous Next
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