TE QUESTION 15 Label each asymmetric carbon in the compound below as Ror S. Çox ноён...
How many asymmetric carbons are present in the compound below? Label each asymmetric carbon in the compound below as R or S. Draw this structure of (S)-1-bromo-1-chioropropane. Take particular care to indicate three-dimensional stereo chemical detail properly. Draw the Fischer projection of (S)-2-bromobutane.
3. Label each asymmetric carbon in the following compounds as either Ror S. (2 point . HHHCl BATCH CH.OH (b) НЕОН CH (c) нс Br н он sort Rors Ros bathe coloriary nе оf он
10) abel each asymmetric carbon in the compound below asR or S HO CH3
5-26 For each structure, 1. star (*) any asymmetric carbon atoms. 2. label each asymmetric carbon as (R) or (S). draw any internal mirror planes of symmetry. label the structure as chiral or achiral. label any meso structures. We were unable to transcribe this image
Label each asymmetric carbon as R or S. HOOC CHỊ CH H 7 H3CF
Draw a three dimensional structure for each compound, and star all asymmetric carbon atoms. Draw the mirror image for each structure, and state whether you have drawn a pair of enantiomers or just the same molecule twice. Draw the enantiomers of 1,3-dibromobutane and label them as (R) and (S).
3. Identify the chiral centers in the diastereomers below and label each as Ror S.
10) 2. Assign Ror Sto the two asymmetric carbons shown below. HO away 4 = toward NH H _NH 5 3. Place an asterisk (*) next to each asymmetric carbon in the molecule shown below CI 5) 4. Calculate the specific rotation for a chance that leatamne ning almland in a 2 decimataru
3. Identify the chiral centers in the diastereomers below and label each as Ror S. CHE
3. Identify the chiral centers in the diastereomers below and label each as Ror S. CH3 CH3