practice-4-revised-key

practice-4-revised-key - Practice Exam 4 - revised...

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Practice Exam 4 - revised (9/23/10) IV. Draw the mirror image of A and determine if it is optically active (circle one). A mirror image III. Show the stereochemistry of each stereocenter by labeling R or S next to it. OMe H Br OH H Me CHO OH H Me HO H HO Me I. Provide the stereochemisty by either R or S conFguration on the designated carbon. Carbon in the back bearing H, Br, and OMe group Carbon in the middle bearing HO and Me II. Given the following compound name, draw a valid structure. 5-( S )-chloro-6-( R )-hepten-3-ol Cl OH (S) (R) enantiomer or meso HO Br H Cl H S S R R
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V. A medicinal chemist discovered a new drug in an optically active form, however not optically pure. The specific rotation of this drug sample was +9.9 degree, and it was later
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This note was uploaded on 10/18/2010 for the course CHEM 322 A taught by Professor Bertolini during the Spring '10 term at USC.

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practice-4-revised-key - Practice Exam 4 - revised...

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