Which of the following Newman projections is the least stable staggered conformation in 3-methylpentane as you look down the bond from C2 to C3? (Me = methyl, Et = ethyl) %3D HEt Et HEt Et Et Me Me Ме Ме H. Meme Me Me H. H. Ме H A E

Which of the following Newman projections is the least stable staggered conformation in 3-methylpentane as you look down the bond from C2 to C3? (Me = methyl, Et = ethyl) %3D HEt Et HEt Et Et Me Me Ме Ме H. Meme Me Me H. H. Ме H A E

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter3: Organic Compounds: Alkanes And Their Stereochemistry

Section3.SE: Something Extra

Problem 46AP: Draw the most stable conformation of pentane, using wedges and dashes to represent bonds coming out...

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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

Which of the following Newman projections is the least stable staggered conformation in
3-methylpentane as you look down the bond from C2 to C3? (Me = methyl, Et = ethyl)
%3D
HEt
Et
HEt
Et
Et
H
Ме
Me
Ме
Me
Me
Meme
Me
H.
Me
H.
H
H.
Me
A
В
E

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