Use the Cahn-Ingold-Prelog rules to establish the priorities of the different groups bondedto the C(2) stereogenic centre in compound X below. Determine the absoluteconfiguration at the C(2) stereogenic centre.6.1[ ]Br+ atomHONH2.C(2).[+ atomic numberCConfiguration:6.2Use the given templates with C1 on the left hand side of the line structures to draw thethree dimensional line structures of (4R)-6,6-dichloro-4-hydroxy-4-methylhexanal andthe enantiomer. Clearly show the configuration of the stereogenic centre.(4R)-6,6-dichloro-4-hydroxy-4-methylhexanalEnantiomer

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Use the Cahn-Ingold-Prelog rules to establish the priorities of the different groups bonded to the C(2) stereogenic centre in compound X below. Determine the absolute configuration at the C(2) stereogenic centre. [ ] [ ] Br atom HO NH2 .C(2). [ ] atomic number X C Configuration:

Use the Cahn-Ingold-Prelog rules to establish the priorities of the different groups bonded to the C(2) stereogenic centre in compound X below. Determine the absolute configuration at the C(2) stereogenic centre. [ ] [ ] Br atom HO NH2 .C(2). [ ] atomic number X C Configuration:

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter12: Chirality

Section: Chapter Questions

Problem 18E

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Question

Use the Cahn-Ingold-Prelog rules to establish the priorities of the different groups bonded
to the C(2) stereogenic centre in compound X below. Determine the absolute
configuration at the C(2) stereogenic centre.
6.1
[ ]
Br
+ atom
HO
NH2
.C(2).
[
+ atomic number
C
Configuration:
6.2
Use the given templates with C1 on the left hand side of the line structures to draw the
three dimensional line structures of (4R)-6,6-dichloro-4-hydroxy-4-methylhexanal and
the enantiomer. Clearly show the configuration of the stereogenic centre.
(4R)-6,6-dichloro-4-hydroxy-4-methylhexanal
Enantiomer

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