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

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Chapter1: Chemical Foundations
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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
Transcribed Image Text: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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