The conformation of rings A, B, C and D in Cholestanol has to be described. Concept Introduction: The conformation structures of six membered rings are given by chair forms. In the chair conformation, all C-C-C bond angles are 110 .9 0 and the hydrogens on the adjacent carbon atoms are staggered with respect to one another. In the chair conformation, no two atoms are closely present, so, there is a little strain present in chair conformation structure of cyclohexane. The C-H bonds in the chair conformation are arranged in axial and equatorial positions. The bonds that are present parallel to the axis are axial bonds and the bonds that are present perpendicular to the axis are equatorial bonds. In cyclohexane, six hydrogens are axial and six hydrogens are equatorial.
The conformation of rings A, B, C and D in Cholestanol has to be described. Concept Introduction: The conformation structures of six membered rings are given by chair forms. In the chair conformation, all C-C-C bond angles are 110 .9 0 and the hydrogens on the adjacent carbon atoms are staggered with respect to one another. In the chair conformation, no two atoms are closely present, so, there is a little strain present in chair conformation structure of cyclohexane. The C-H bonds in the chair conformation are arranged in axial and equatorial positions. The bonds that are present parallel to the axis are axial bonds and the bonds that are present perpendicular to the axis are equatorial bonds. In cyclohexane, six hydrogens are axial and six hydrogens are equatorial.
The conformation of rings A, B, C and D in Cholestanol has to be described.
Concept Introduction:
The conformation structures of six membered rings are given by chair forms. In the chair conformation, all C-C-C bond angles are 110.90 and the hydrogens on the adjacent carbon atoms are staggered with respect to one another. In the chair conformation, no two atoms are closely present, so, there is a little strain present in chair conformation structure of cyclohexane. The C-H bonds in the chair conformation are arranged in axial and equatorial positions. The bonds that are present parallel to the axis are axial bonds and the bonds that are present perpendicular to the axis are equatorial bonds. In cyclohexane, six hydrogens are axial and six hydrogens are equatorial.
(b)
Interpretation Introduction
Interpretation:
The hydroxyl group present on Ring A is either axial or equatorial has to be given.
Concept Introduction:
The C-H bonds in the chair conformation are arranged in axial and equatorial positions. The bonds that are present parallel to the axis are axial bonds and the bonds that are present perpendicular to the axis are equatorial bonds. In cyclohexane, six hydrogens are axial and six hydrogens are equatorial.
(c)
Interpretation Introduction
Interpretation:
The methyl group present at the junction of Ring A and Ring B is either axial or equatorial to Ring A and Ring B has to be given.
Concept Introduction:
The C-H bonds in the chair conformation are arranged in axial and equatorial positions. The bonds that are present parallel to the axis are axial bonds and the bonds that are present perpendicular to the axis are equatorial bonds. In cyclohexane, six hydrogens are axial and six hydrogens are equatorial.
(d)
Interpretation Introduction
Interpretation:
The methyl group present at the junction of Ring C and Ring D is either axial or equatorial has to be given.
Concept Introduction:
The C-H bonds in the chair conformation are arranged in axial and equatorial positions. The bonds that are present parallel to the axis are axial bonds and the bonds that are present perpendicular to the axis are equatorial bonds. In cyclohexane, six hydrogens are axial and six hydrogens are equatorial.
Consider the synthesis. What is compound Y? Please explain what is happening in this question. Provide a detailed explanation and a drawing to show how the compound Y creates the product. The correct answer is D.
What would be the major product of the following reaction? Please include a detailed explanation of what is happening in this question. Include steps and a drawing to show this reaction proceeds and how the final product is formed. The correct answer is B. I put answer D and I don't really understand what is going on in the question.
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Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning