(S)-2-hydroxypropanoic acid lactic acid) is produced in the fermentation of milk to make yogurt. Some bacteria produce a mixture of sterecisomers 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. OH ÕH

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Chapter1: Chemical Foundations
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(S)-2-hydroxypropanoic acid (lactic acid) is produced in the
fermentation of milk to make yogurt. Some bacteria produce
a mixture of sterecisomers 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.
OH
Transcribed Image Text:Work Screen (S)-2-hydroxypropanoic acid (lactic acid) is produced in the fermentation of milk to make yogurt. Some bacteria produce a mixture of sterecisomers 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. OH
Work Screen
Draw the enantiomer of the molecule shown below. Use a
dash or wedge bond to indicate stereochemistry of
substituents on asymmetric centers, where applicable.
"NH2
Draw the Enantiomer
Transcribed Image Text:Work Screen Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. "NH2 Draw the Enantiomer
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