(i) The enantiomer of the "SRS" biological molecule should be designated "RSR"
(ii) Both the higher priority groups on each carbon (F, Cl) are present on the same side of the C=C plane. Hence, the given isomer is a Z-isomer.
The corresponding E-isomer will be the alkene in which both F and Cl are present on the opposite sides of the C=C plane, i.e. either you can reverse exchange H and F on the left-side carbon or you can exchange OH and Cl on the right-side carbon.
QUESTION 14 A biological molecule with three chirality centers is designated "SRS using the Cahn-ingold-Prelog labeling...
Using the Cahn-Ingold-Prelog system, what are the configurations about the two chiral centers in the carbohydrate, Threose shown below? HC (1) HO H (2) H ОН CH OH Threose a. C(1) - R and C(2) - S b. C(1) = Z and C(2) - Z cC(1) = R and C(2) - R d. C(1) = E and C(2) = E e. C(1) = E and C(2) = Z of. C(1) = S and C(2) - S 8.C(1) = Z and...
please explain why the answers are what they are. thank you 18. Which one of these molecules does not contain any stereogenic centers? 19. How do the two chemical structures shown in the box below compare to one another? a) They represent the same molecule. b) They are isotopes. (c) They are constitutional isomers. d) They have different chemical formulas. 23. Based on structural characteristics, predict which of these substances has the lowest melting point @woo woo Dance CH 3....