6. Assign R or S stereochemistry to the chirality centers in the molecule below. (2 P! OH
Assign the stereochemistry (R or S) on each of chirality centers in the molecules below and draw the enantiomer of each compound.
s. Assign the R or s stereochemistry to the chirality centers in ascorbic acid (vitamin C)? 4pts OH HO HO OH
Assign R or S configuration to the chirality centers in the molecule below. Configuration of CA: Configuration of CB: Configuration of C_A: Configuration of C_B:
Assign R or S stereochemistry to the chirality centers in these Newman structures. Determine if these molecules are chiral. achiral. or meso compound
Assign R or S configuration to the chirality centers in the molecules below. CI OH нон -CH₃ OROS OROS
Exhibit 5-2 Place asterisks at all the chirality centers in each molecule below. H oH OH ill NHCH₂ NHCH3 phedrine COOH thromboscane A, OH Exhibit 5-3 Assign R, S configurations to each indicated chirality center in the B. lcoor HO. A. S OHO -H9 | 2 CHÁNH,3 all 0 о HO HO ů oth Nty alarine som brine
Assign the Stereochemistry for the chiral centers present in these compounds as R or S 5. Assign the stereochemistry for the chiral centers present in these compounds as Ror S: (7 points) HO HO HO COOH CH OH
For the following compound, assign the configuration (R or S) of each of the chirality centers from top to bottom. CHO H OH H OH HO H СН,ОН Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a R, R, S b S, S,R с S, R, S
Find and circle all chirality centers in each molecule and designate R or S configuration for each chirality center. 애 HEH HECH3 ОН
1. Draw the two enantiomers of trans-1,2-Diaminocyclohexane and assign stereochemistry (R or S) to both of the chirality centers in each of the enantiomers.