Exhibit 5-2 Place asterisks at all the chirality centers in each molecule below. H oH OH ill NHCH₂ NHCH3 phed...
double bond could never be a chiral center
7.(10 points)Place asterisks at all the chirality centers in each molecule below. COOH HO OH prostaeyelin
6. Assign R or S stereochemistry to the chirality centers in the molecule below. (2 P! OH
Assign R, S configurations to each indicated chirality center in the molecules below. A. OH B. COOH НО. ---H co CHANH CH; HAN HO H norepinephrine alaine 0 D. C. H E. HOC OH moje H н. CH3 H2C H НО CO H CH2 tartaric acid dihydrocaryone
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...