3 - 48Convert each Newman projection to the equivalent line angle formula, and assign the IUPAC namef)g) (f)(g)FCH3CH3CBR3FH.H.HH.H.CH(CH3)2H.Draw Newman projections along the C3-C4 bond3-ethyl-2,4,4-trimethylheptane.Conformational studies on ethane-1,2-diol (HOCH2C-C bond to be the gauche conformation, which isDraw Newman projections of these conformers, andThe most stable form of the common sugar glucosesubstituents equatorial. Draw this most stable confor*3-49|*3-503-51HO.HO3-52This is a Newman poiection of a substituted cyclohe(a) Draw the equivalent chair form.(b) Draw the equivalent structure using wedge and(c) Give the IUPAC name.BrH.HH

Line-Angle formula also known as wedge-dash formula. To convert Newman projection formula to line…

Answered: (g) CH3 CH3 H. CB33 H. H. H. CH(CH3)2…

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(g) CH3 CH3 H. CB33 H. H. H. CH(CH3)2 H.

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 47AP: The diaxial conformation of cis-1, 3-dimethylcyclohexane is approximately 23 kJ/mol (5.4 kcal/mol)...

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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

3 - 48 Convert each Newman projection to the equivalent line angle formula, and assign the IUPAC name f) g)

(f)
(g)
F
CH3
CH3
CBR3
F
H.
H.
H
H.
H.
CH(CH3)2
H.
Draw Newman projections along the C3-C4 bond
3-ethyl-2,4,4-trimethylheptane.
Conformational studies on ethane-1,2-diol (HOCH2
C-C bond to be the gauche conformation, which is
Draw Newman projections of these conformers, and
The most stable form of the common sugar glucose
substituents equatorial. Draw this most stable confor
*3-49
|
*3-50
3-51
HO.
HO
3-52
This is a Newman poiection of a substituted cyclohe
(a) Draw the equivalent chair form.
(b) Draw the equivalent structure using wedge and
(c) Give the IUPAC name.
Br
H.
H
H

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For 1,2-dichloroethane: a.Draw Newman projections for all eclipsed conformations formed by rotation from 0° to 360° about the carbon-carbon single bond. b.Which eclipsed conformation(s) has (have) the lowest energy? Which has (have) the highest energy? c.Which, if any, of these eclipsed conformations are related by reflection?
For 1,2-dichloroethane: ( Q.) Draw Newman projections for all eclipsed conformations formed by rotation from 0° to 360° about the carbon-carbon single bond.
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Please help show and explain: All confirmations of 2-chloro-3methylbutane looking down the C1-C2 bond and 1 staggered confimation looking down the C2-C3 bond (Label all and rank all from least to most stable)
What does the most stable Newman Projection of 2,2 dimethyl hexane look like?