Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
bartleby

Concept explainers

Question
Book Icon
Chapter 16.3, Problem 4P

(a)

Interpretation Introduction

Interpretation:

A sugar that is C3 epimer of D-xylose is to be stated.

Concept Introduction:

Epimer: Epimer is one of a pair of stereoisomers. Epimers are the monosaccharides which differ in the structure at only one of the asymmetric center and they are particular kind of stereoisomers that are not enantiomers. For example,D-xylose and D-ribose are the C3 epimers because they differ in the configuration only at carbon number 3 starting from the above rest whole structure is same.

b)

Interpretation Introduction

Interpretation:

A sugar that is C5 epimer of D-allose is to be stated.

Concept Introduction:

Epimer: Epimer is one of a pair of stereoisomers. Epimers are the monosaccharides which differ in the structure at only one of the asymmetric center and they are particular kind of stereoisomers that are not enantiomers. For example,D-xylose and D-ribose are the C3 epimers because they differ in the configuration only at carbon number 3 starting from the above rest whole structure is same.

c)

Interpretation Introduction

Interpretation:

A sugar that is C4 epimer of L-gulose is to be stated.

Concept Introduction:

Epimer: Epimer is one of a pair of stereoisomers. Epimers are the monosaccharides which differ in the structure at only one of the asymmetric center and they are particular kind of stereoisomers that are not enantiomers. For example,D-xylose and D-ribose are the C3 epimers because they differ in the configuration only at carbon number 3 starting from the above rest whole structure is same.

d)

Interpretation Introduction

Interpretation:

A sugar that is C4 epimer of D-lyxose is to be stated.

Concept Introduction:

Epimer: Epimer is one of a pair of stereoisomers. Epimers are the monosaccharides which differ in the structure at only one of the asymmetric center and they are particular kind of stereoisomers that are not enantiomers. For example,D-xylose and D-ribose are the C3 epimers because they differ in the configuration only at carbon number 3 starting from the above rest whole structure is same.

Blurred answer
Students have asked these similar questions
CH2OH A. Circle the anomeric sugar on the left OH B. Circle the carbon that makes the H. H. given sugar D-configuration? H. C. Is this possibly a natural sugar? OH D. Is this a or B sugar? H. OH
How is each compound related to the simple sugar D-erythrose? Is it an enantiomer, a diastereomer, or an identical molecule?
5-Deoxyglucose will close to a?
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY