(S)-2-hydroxypropanoic acid (lactic acid) is produced in the fermentation of milk to make yogurt. Some bacteria produce a mixture of stereoisomers and some produce solely the (R)-isomer. (S)-lactic acid is shown below. Draw the (R)-isomer. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. esc O OH Drawing 124,538 OH 8.0 OCT = D. stv Atoms, Bonds and Rings OH J @ Br 00 SA 8 Charges @D D-11 NH₂ ((( Ï DD H a

(S)-2-hydroxypropanoic acid (lactic acid) is produced in the fermentation of milk to make yogurt. Some bacteria produce a mixture of stereoisomers and some produce solely the (R)-isomer. (S)-lactic acid is shown below. Draw the (R)-isomer. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. esc O OH Drawing 124,538 OH 8.0 OCT = D. stv Atoms, Bonds and Rings OH J @ Br 00 SA 8 Charges @D D-11 NH₂ ((( Ï DD H a

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter23: Amines

Section: Chapter Questions

Problem 23.22P

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