Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Chapter 29.8, Problem 16P
Interpretation Introduction

Interpretation: The enantiomer and any two diastereomers of cholesterol are to be drawn, and the position for OH group of cholesterol as an axial or equatorial is to be identified.

Concept introduction: Steroids, a group of tetracyclic lipids composed of one five-membered ring and three six-membered rings. Thesse rings are lettered by A, B, C, and D. Most of the steroids contain two angular methyl groups. These methyl groups are numbered as C18 and C19 respectively.

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D The following disaccharide contains a(n) (blank]-glycosidic linkage. HO CH₂OH ОН Oa-1,4 OB-1,4 a-1,6 O B-1,6 0 OH Question 6 double bond ssignments/syllabus ester bond ether bond amide bond HO A glycosidic bond between two monosaccharides can also be classified as a(n) [blank). OH OH Melebi OH MacBook Pro
In glycoside formation, the hemiacetal functional group of a cyclic monosaccharide is converted to an acetal group by reaction with a(an)
Which characteristic is shared by the ring forms of the given monosaccharides? * CH2OH CHO O= H- HO- HO- но- H- но- Но H H- -OH ČH,OH ČH2OH Both exist mainly as furanoses. Both contain a hemiacetal bond. Both can undergo mutarotation. O Both exist mainly as pyranoses.
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