9) Below is a statin, simvastatin, used for treating high cholesterol. Assign the stereochemical configuration of the selected tetrahedral carbon chiral centers (R, S or N (not a chiral center)) and the alkene (E, Z or N (not a stereocenter)) that are indicated by the arrows (note that you do not have to assign the configuration of every chiral center in the molecule). If the atom in question is not a chiral center or is not a stereocenter circle N for neither. RS N RS N HO RS N I RS N RS N RS N EZ N EZ N

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9) Below is a statin, simvastatin, used for treating high cholesterol. Assign the stereochemical configuration of
the selected tetrahedral carbon chiral centers (R, S or N (not a chiral center)) and the alkene (E, Z or N (not a
stereocenter)) that are indicated by the arrows (note that you do not have to assign the configuration of every
chiral center in the molecule). If the atom in question is not a chiral center or is not a stereocenter circle N for
neither.
RS N
RS N
HO
RS N
I
RS N
RS N
RS N
EZ N
EZ N
Transcribed Image Text:9) Below is a statin, simvastatin, used for treating high cholesterol. Assign the stereochemical configuration of the selected tetrahedral carbon chiral centers (R, S or N (not a chiral center)) and the alkene (E, Z or N (not a stereocenter)) that are indicated by the arrows (note that you do not have to assign the configuration of every chiral center in the molecule). If the atom in question is not a chiral center or is not a stereocenter circle N for neither. RS N RS N HO RS N I RS N RS N RS N EZ N EZ N
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