1) diastereomers due to having cis and trans geometry
2) enantiomers due to having S and R configuration
3) diastereomers due to not mirror images
4)enantiomers due to being mirror images.
5-6 5. (8 pts.) Identify the relationship between the following pair as enantiomer, diastereomer or same...
(8 pts.) Identify the relationship between the following pair as enantiomer, diastereomer or same compound 5. 1) and Br Br and 2) Br 3) H and H H 4) and
(8 pts.) Identify the relationship between the following pair as enantiomer, diastereomer or same compound. 5. Br 1) Diastereomners and Br F X H Same compond 2) and Br Br 43с н, 3) Fil and н CH3 Diastereomers Br and Enantiomers
6. (4 pts.) Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more potent than any of its other stereoisomer. OH ethambutol
6. (4 pts.) Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more potent than any of its other stereoisomer. ОН 21 ОН ethambutol
(4 pts.) Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more potent than any of its other stereoisomer. 6. OH OH ethambutol
19) (9 pts) Identify the relationship between each pair of structures shown A) same compound, B) constitutional isomers, C) conformational isomers, D) configurational isomers or E) enantiomers. CH B CH and Answer *To receive full credit, label each as R or S. b. Answer: Cl Br CH3 *To receive full credit, label each as R or S. c. Answer o (5 pts) Determine the formal charge on the indicated atoms. HzN-N a. : Br: b.
diastereomer 8. (1 pt.) Identify the specific type of relationship between each of the following pairs of molecules (i.e., either the same, constitutional isomers, enantiomers, diastereomers, conformers or unrelated). Br HOM Br Br a) b) d) H OH CL c HO- -Hi Be H- OH HO H e) f)
5. Determine the relationship between each pair in the following set of compounds: same compound, enantiomers or diastereomers. (2 points each) CHs CH CH CHS H CHLCH Br CHS H Br H CH H Br
1. For each pair, circle the molecule with the lower pK and provide a brief explanation for your choice. wale wabon ---- 2. For each molecule, draw the two possible chair conformers and circle the preferred conformer. a) cis-1,3-dimethylcyclohexane trans-1,4-dimethylcyclohexane 3. Draw all distinct isomers of dimethylcyclopropane and show the relationship as enantiomer, diastereomer or meso. 4. In each of the following pairs of compounds one is chiral and the other achiral, Circle the chiral compound in each. a) CH,CHCH=CH...
Give the stereochemical relationship between each pair of structures. 9:23 X Additional Ch. 6 Review Problems.d... ... Name: 1) Give the stereochemical relationships between cach pair of structures: same compound, constitutional structural isomers, enantiomers, diastereomers. Any E- 2) Which of the following molecules, if isolated in its pure form, would demonstrate optical activity? Circle your selected answers). 3) For each structure: I. Star () any asymmetric carbon atoms. II. Label each asymmetric carbon as Ror S. To receive full credit,...