Convert each Newman projection to the equivalent line angle formation and assigne the IUPAC name c) d)

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry
Section4.SE: Something Extra
Problem 24VC: A trisubstituted cyclohexane with three substituents-red, green, and blue-undergoes a ring-flip to...
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Convert each Newman projection to the equivalent line angle formation and assigne the IUPAC name c) d)
itution
ated bond to draw the most stab
bond
cis-1,3-dimethylcyclohexane, and label all the positions
n and the lower-energy conformation.
nformations has been measured to be about 23 kJ (5,4 k
to the torsional energy of gauche relationships?
onal steric strain of the 1,3-diaxial interaction?
compound, and label the substituents as axial and equa
ole.
(b) trans-1-ethyl-2-isopropylcyclohexane
(d) trans-1-ethyl-3-methylcyclohexane
(f) trans-1-ethyl-4-methylcyclohexane
ional energetics of substituted cyclohexanes, predict
ning.
uivalent line-angle formula, and assign he IUPAC r
(b) 3,3-dimethylhexane ab
(c)
(d)
Br
CH2CH3
H.
H.
CH3
CI
H
H.
CH2CH3
H
CH3
CH(CH3)2
(h)
H.
(i)
Transcribed Image Text:itution ated bond to draw the most stab bond cis-1,3-dimethylcyclohexane, and label all the positions n and the lower-energy conformation. nformations has been measured to be about 23 kJ (5,4 k to the torsional energy of gauche relationships? onal steric strain of the 1,3-diaxial interaction? compound, and label the substituents as axial and equa ole. (b) trans-1-ethyl-2-isopropylcyclohexane (d) trans-1-ethyl-3-methylcyclohexane (f) trans-1-ethyl-4-methylcyclohexane ional energetics of substituted cyclohexanes, predict ning. uivalent line-angle formula, and assign he IUPAC r (b) 3,3-dimethylhexane ab (c) (d) Br CH2CH3 H. H. CH3 CI H H. CH2CH3 H CH3 CH(CH3)2 (h) H. (i)
Expert Solution
Step 1 Newman to bond line convertion

 

In the first step convert the given newman projection formula into bond line

In newman projection front carbon is represented with dot and back carbon as circle, it visualizes the conformation of  chemical bond from front to back, This 3D representation of a compound is useful in alkane stereochemistry 

 

In the second step asssign name according to IUPAC rules

 

 

 

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