How to solve this question? Would the most stable conformation be staggered (and is it gauche or anti? I can't tell), and the least stable be eclipsed? Not sure how to draw these structures. decipsed11)From the perspective of viewing down the C2-C3 bond,draw the Newman projection of the least stable and the moststable conformation of 2,3-dimethylbutane. Explain why theC2C3conformer is the most and the least stable.

edipsed 11) From the perspective of viewing down the C2-C3 bond, draw the Newman projection of the least stable and the most stable conformation of 2,3-dimethylbutane. Explain why the C2 C3 conformer is the most and the least stable. CH

edipsed 11) From the perspective of viewing down the C2-C3 bond, draw the Newman projection of the least stable and the most stable conformation of 2,3-dimethylbutane. Explain why the C2 C3 conformer is the most and the least stable. CH

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 55AP: myo-Inositol, one of the isomers of 1,2,3,4,5,6-hexahydroxycyclohexane, acts as a growth factor in...

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

How to solve this question? Would the most stable conformation be staggered (and is it gauche or anti? I can't tell), and the least stable be eclipsed? Not sure how to draw these structures.

decipsed
11)From the perspective of viewing down the C2-C3 bond,
draw the Newman projection of the least stable and the most
stable conformation of 2,3-dimethylbutane. Explain why the
C2
C3
conformer is the most and the least stable.

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As the energy of the compound increases, stability of that conformation decreases.

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