What are the R and S configurations of each of these molecules oH Ho Y OH...
3. R, S Configurations Assign R, S configurations to each indicated chirality center in the molecules below. 14. OH 15. COOH ---H CH NH2 HỌN H -CH3 HO alanine norepinephrine - 18. 16. HOC / OHH HV CH; НС . H7 HO COH CH2 dihydrocarvone tartaric acid
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
Assign R, S configurations to each indicated che e se A. OH! HO TTCH NH, merupp hale HOC / OH H HO HC COZH acid tarber CH, 1. The configuration of this carbon atom (A) is 2. The configuration of this carbon atom (B) is 3. The configuration of this carbon atom (E) is Consider the structure of streptimidone to answer the following question(s). OH OH strep timidone H3C H 4. Assign R or S configuration to each chirality center...
Assign R/S configurations to each chiral center in the following molecules. Clearly label the stereocenter and show your priority ranking. If no chiral centers exist, write "achiral." (15 pts) GEHICH ANTICHE VSH он "CH, HjC NH2 OH
Assign R, S configurations to each indicated chirality center in the molecules below. B. COOH A. OH HOW -H CHANH HNCH HO norepinephrine alamine HOC / OH CH3 не HC HÓ COH tartaric acid CH2 dihadrocarpone The configuration of this carbon atom (A) is · (2 pts.) The configuration of this carbon atom (B) is _ . (2 pts.) The configuration of this carbon atom (C) is . (2 pts.) . The configuration of this carbon atom (D) is __....
4. For each pair of molecules, assian the confiquration at each chiral center as R or S Give the relationship between the pair of molecules es no relation, constitutional isomers, same molecule but not meso, some molecule and meso, enantiomers, or diastereomerS There should only be one possible answer. OH OH Constitutiona Soenars b. Br Br c. NH2 NH2 NH2 NH2 d. HO. но. ШЕи ши.
(4) 18. (R)-(+)-Glyceraldehyde: ну HO HC-OH A: is levorotatory. B: rotates plane-polarized light in a counterclockwise direction. C: rotates plane-polarized light in a clockwise direction. D: is racemic. (10) 19. Assign R.S configurations to each indicated stereogenic center in the molecules below. OH HO 1. Н -NH₂ MOH HO norepinephrine CEO trans-cyclopentane-1,2-diol COOH +05 H- 08 COCA mero tortor ardd FOT CH OH Blyamaldehyde D b) _
Consider the following molecules: CH3O CHE NH2 -CH-C-OH NH-CH-CH2-OH CH3 Сн, о O= Il HO-CH=C=OH. HO-C-CH-C-OH CHE i. Which of the molecules above is a secondary amine? [Select il. Which of the molecules above will be a zwitterion under physiological conditions (pH 7)? (Select) ill. Which of the molecules above has two acidic protons? Select
assign all stereochemistry (R or S and E or Z) for the
molecules below
04 -NH₂ 옆 요 외 앨 y Ho Brite ) THOM Bril "NH₂ Fa u OH OH 아 | 8. 1
What is the product of the following reaction?
"NH2 OH "OH H N HO NH HO — II