3) a) Convert the following perspective diagram to a Fischer projection. Give R/S designations to each of the chirality centers in your Fischer projection, being sure to clearly show your Cahn-Ingold- Prelog priorities: H. Br H H3C HO b) Convert the following Fischer projection to a perspective diagram. Give R/S desigantions to each of the chirality centers in your perspective diagram, being sure to show your Cahn-Ingold- Prelog priorities: CH3 -H H- -F ČH3 c) Draw Fischer projections of all stereoisomers of the compound shown above in b). Designate them as enatiomers or diastereomers, and show mirror planes as appropriate in your illustrations.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter12: Chirality
Section: Chapter Questions
Problem 3E
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3) a) Convert the following perspective diagram to a Fischer projection. Give R/S designations to
each of the chirality centers in your Fischer projection, being sure to clearly show your Cahn-Ingold-
Prelog priorities:
Br H
Br
H3C
CI
b) Convert the following Fischer projection to a perspective diagram. Give R/S desigantions to
each of the chirality centers in your perspective diagram, being sure to show your Cahn-Ingold-
Prelog priorities:
CH3
F
H.
-F
c) Draw Fischer projections of all stereoisomers of the compound shown above in b). Designate
them as enatiomers or diastereomers, and show mirror planes as appropriate in your illustrations.
Transcribed Image Text:3) a) Convert the following perspective diagram to a Fischer projection. Give R/S designations to each of the chirality centers in your Fischer projection, being sure to clearly show your Cahn-Ingold- Prelog priorities: Br H Br H3C CI b) Convert the following Fischer projection to a perspective diagram. Give R/S desigantions to each of the chirality centers in your perspective diagram, being sure to show your Cahn-Ingold- Prelog priorities: CH3 F H. -F c) Draw Fischer projections of all stereoisomers of the compound shown above in b). Designate them as enatiomers or diastereomers, and show mirror planes as appropriate in your illustrations.
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