10Select the substituent with the highest priority in the R/S system. NA. -CH2CH=OB. -CH=0C. -CH2CH2OHD. -CH2OCH3E. -CH2OHWhich one of the following describes the correct stereochemical conformation ofthis molecule. NAttachmentsH₂C.CH₂CH3A.(2R,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-oneB. (2R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one(2S,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-oneC.D. The molecule is achiral and the absolute configuration can therefore notbe assigned.E. (25,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one

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Select the substituent with the highest priority in the R/S system. M A. -CH2CH=O B. -CH=0 C. -CH2CH2OH D. -CH2OCH3 E. -CH2OH

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter10: Oxidation And Reduction

Section: Chapter Questions

Problem 4CTQ

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Concept explainers

Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.

Question

10
Select the substituent with the highest priority in the R/S system. N
A. -CH2CH=O
B. -CH=0
C. -CH2CH2OH
D. -CH2OCH3
E. -CH2OH
Which one of the following describes the correct stereochemical conformation of
this molecule. N
Attachments
H₂C.
CH₂
CH3
A.
(2R,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one
B. (2R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one
(2S,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one
C.
D. The molecule is achiral and the absolute configuration can therefore not
be assigned.
E. (25,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one

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