label each asymmetric carbon in the ** OH HO enantiomer. 8) Label each asymmetric carbon in the

label each asymmetric carbon in the

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** OH HO enantiomer. 8) Label each asymmetric carbon in the compound below as R or S. CH3 CH3 OH CH3 9) Label each asymmetric carbon in the compound below as R or S. OH H * H OH 10) Label each assymetric carbon in the compound below as R or S. CI 11) Draw the structure of (2R,3S)-2,3-dichloropentane. Take particul dimensional stereochemical detail properly. 12) Draw the structure of (S)-1-bromo-1-chloropropane. Take partic dimensional stereochemical detail properly. 13) Draw the structure of a meso form of 1,3-dichlorocyclopentane. indicate three-dimensional stereochemical detail properly. nummetric carbons are present in the compound be ** OH HO enantiomer. 8) Label each asymmetric carbon in the compound below as R or S. CH3 CH3 OH CH3 9) Label each asymmetric carbon in the compound below as R or S. OH H * H OH 10) Label each assymetric carbon in the compound below as R or S. CI 11) Draw the structure of (2R,3S)-2,3-dichloropentane. Take particul dimensional stereochemical detail properly. 12) Draw the structure of (S)-1-bromo-1-chloropropane. Take partic dimensional stereochemical detail properly. 13) Draw the structure of a meso form of 1,3-dichlorocyclopentane. indicate three-dimensional stereochemical detail properly. nummetric carbons are present in the compound be