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- Rank the following groups in order of decreasing priority. −CH2CH3, −CH3, −H, −CH(CH3)2For the given ee values, calculate the percentage of each enantiomer present.a. 90% eeb. 99% eec. 60% eeOn the molecule below, highlight all R stereocenters in red and all S stereocenters in blue. If it doesn't contain any stereocenters, check the "No Stereocenters" box under the drawing area.
- As a fischer projection is the compound R or S and which group is the highest priority ?Explain how R and S are related to (+) and (-).Use Apendix C or Figure 18.9 to determine whether Kc > 1 or Kc < 1 for each reaction. (a) H2SO3 + NH3 HSO3- + NH4+ Kc < 1 or Kc > 1 (b) HCN + HCO3- H2CO3 + CN - Kc < 1 or Kc > 1
- Please help Selected 1 chiral center drug. What is the compound you selected? Is it legal or illegal? Is it over the counter or prescription only? If legal, what types of human or animal conditions does the drug you selected treat? If illegal, what is the most common reason people will choose to take it? How safe is it to use the compound you selected? How many chiral centers does the drug you selected contain? Are the chiral centers in the drug you selected R or S?When determining R AND S rank these groups from highest to lowest priorityI was wondering if theres an error in the answer booklet. Because we have a double bond so I thought it was E and 3S because of the stereocenter?
- t please don't provide handwriting solution it's understandable that CH3 is ortho/para directing. but which of the two ortho positions would the Br stick to?Hello good morning, we only saw very little of this topic and I did not understand it and this was an activity that he left us as homework, I will quote it as it is, I hope you can help me. Monosodium (S)-glutamate [α]_D^(25°C)=+24, is the active potentiator of flavor known as MSG. The condensed formula of MSG is this. 1. Draw the structure of the S-enentiomer of MSG.2. If a commercial sample of MSG had an [α]_D^(25°C)=+10, what would be the enantiomeric excess, what would be the percentage of the S and R enantiomers in the mixture?Can someone help me draw an R configuration for this compound?
