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(S)-2-hydroxypropanoic acid (lactic acid) is produced in the fermentation of milk to make yogurt. Some bacteria produce a mix
Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asym
Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asym
Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asym
Draw both of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of
(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 \( (\mathrm{R})- \) 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. Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Draw both of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.


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Answer- Enantiomers are non-superimposable mirror
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