3. Identify the chiral centers in the diastereomers below and label each as Ror S. CH3...
3. Identify the chiral centers in the diastereomers below and label each as Ror S.
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 R or S.
1. Identify all the chiral centers in the y all the chiral centers in the molecule below: 2. For each of the pairs of compounds, de indicate if they are identical, enantiomers, diastereomers, constitutional isomers or different compounds. 3. Identify the chiral centers in the diastereomers below and label each as R or S.
2. For each of the pairs of compounds, indicate if they are identical, enantiomers, diastereomers, constitutional isomers or different compounds. Z-bromopropaneitrite Br CN constitutional isomers H2CH... CN CH3 CH3 COH Hanc HC HEN HS o n diastereomers MMCH₂CH₃ CH3 3. Identify the chiral centers in the diastereomers below and label each as Ror S. CHE
Label the chiral centers in the below molecule as (R) or (S) in the boxes provided and clearly indicate your priorities of groups attached to each of the chiral centers (see arrows). (8 points) CH3 CH-CH3 CSH Fhimu HO CHE
1. (23 pts.) Label each stereocenter (chiral center) as Ror S. Label each molecule as chiral or achiral. CH ен-он H- CH3 . Он CH2OH Сн,он h) н он В ньон нон НО-Б-н ен,он но- н H-LOH CH OH
Identify the absolute configuration of the chirality centers in each of the following compounds as Ror S. Note: if multiple chirality centers are present, indicate the stereochemical designations as: RR, SS, RS, or SR (Other terms used for chirality center include chiral center, stereocenter, and stereogenic center.)
6. Assign the absolute configuration of all chiral carbon centers as Ror S. о она ОН Н І но, N-CH3 но-НН b. Hd Сн,он но nicotine adrenaline
Determine if the indicated chiral center is in the Ror S configuration. H CH3