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17 Nov 2019
Best answer. Any explanation would be appreciated!
The incorrect statement from the thiophenol/phenol equilibrium below would be: the (1 rightarrow r) reaction predominates over the (r rightarrow 1) the value of K_eq is ~ 10^9.4 phenol is a stronger acid than thiophenol each conjugate base is able to delocalize charge via resonance the sulfur anion is larger than the oxygen anion and better bears the negative charge The molecule below is the ester form of Travaprost, which is used in the treatment of the eye disorder "open-angle" glaucoma. The number of stereocenters in this molecule is and the number of possible stereoisomers would be 3; 8 5; 32 7; 128 2; 4 4; 16 Referring back to 5, and Travaprost, the incorrect statement below would be: the molecule comprises two alkene functional groups, one cis and one trans each -OH group resides at an R stereocenter the value of DU is 8 the three hydroxy groups will likely impart water solubility the molecular formula is C_26H_35F_3O_6
Best answer. Any explanation would be appreciated!
The incorrect statement from the thiophenol/phenol equilibrium below would be: the (1 rightarrow r) reaction predominates over the (r rightarrow 1) the value of K_eq is ~ 10^9.4 phenol is a stronger acid than thiophenol each conjugate base is able to delocalize charge via resonance the sulfur anion is larger than the oxygen anion and better bears the negative charge The molecule below is the ester form of Travaprost, which is used in the treatment of the eye disorder "open-angle" glaucoma. The number of stereocenters in this molecule is and the number of possible stereoisomers would be 3; 8 5; 32 7; 128 2; 4 4; 16 Referring back to 5, and Travaprost, the incorrect statement below would be: the molecule comprises two alkene functional groups, one cis and one trans each -OH group resides at an R stereocenter the value of DU is 8 the three hydroxy groups will likely impart water solubility the molecular formula is C_26H_35F_3O_6
Tod ThielLv2
20 Apr 2019