Exam 2 FS07-Blank - 1. (20 pts) Consider compound A at...

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2 1. (20 pts) Consider compound A at right: (a) (3 pts) Name A , being sure to include stereochemical ( R S ) designations. (b) (3 pts) On the template below, make a Newman projection of the eyeball’s view of A . (c) (4 pts) Redraw A (upper left) in the table below, together with its three stereoisomers. A B C D (d) (4 pts) On the templates below, make Fischer projections of A-D from part (c). A B C D (e) (6 pts) Among the four compounds you drew in (d) assign all stereochemical relationships (enantiomer, diastereomer, etc) by circling the correct term. A to B Enantiomers Diastereomers Other (define) A to C Enantiomers Diastereomers Other (define) A to D Enantiomers Diastereomers Other (define) B to C Enantiomers Diastereomers Other (define) B to D Enantiomers Diastereomers Other (define) C to D Enantiomers Diastereomers Other (define) Cl Br A
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3 2. (20 pts) Draw the structures of the major organic product(s) of the following reactions. Remember that double bonds have two equally reactive faces with exposed
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Exam 2 FS07-Blank - 1. (20 pts) Consider compound A at...

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