EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
Question
Book Icon
Chapter 23, Problem 23.48SP

(a)

Interpretation Introduction

To determine: The name of the given aldose.

Interpretation: The name of the given aldose is to be stated.

Concept introduction: The two diastereomeric sugars which differ only in the configuration at a single asymmetric carbon atom are known as epimers. Aldose is a monosaccharide which contains an aldehyde carbonyl group.

(b)

Interpretation Introduction

To determine: The name of the given aldose.

Interpretation: The name of the given aldose is to be stated.

Concept introduction: The two diastereomeric sugars which differ only in the configuration at a single asymmetric carbon atom are known as epimers. Aldose is a monosaccharide which contains an aldehyde carbonyl group.

(c)

Interpretation Introduction

To determine: The name of the given aldose.

Interpretation: The name of the given aldose is to be stated.

Concept introduction: The two diastereomeric sugars which differ only in the configuration at a single asymmetric carbon atom are known as epimers. Aldose is a monosaccharide which contains an aldehyde carbonyl group.

(d)

Interpretation Introduction

To determine: The name of the given aldose.

Interpretation: The name of the given aldose is to be stated.

Concept introduction: The two diastereomeric sugars which differ only in the configuration at a single asymmetric carbon atom are known as epimers. Aldose is a monosaccharide which contains an aldehyde carbonyl group.

(e)

Interpretation Introduction

To determine: The name of the given aldose.

Interpretation: The name of the given aldose is to be stated.

Concept introduction: The two diastereomeric sugars which differ only in the configuration at a single asymmetric carbon atom are known as epimers. Aldose is a monosaccharide which contains an aldehyde carbonyl group.

Blurred answer
Students have asked these similar questions
Which of the following best describes the disaccharide shown here? HO. он, но OH OH HO A. a-1,4' glycoside of D-glucose and D-galactose B. B-1,3' glycoside of D-glucose and D-galactose C. a-1,4' glycoside of D-galactose and D-glucose D. B-1,4' glycoside of D-gulose and D-galactose E. a-1,3' glycoside of D-allose and D-glucose F. a-1,3' glycoside of D-idose and D-idose G. a-1,3' glycoside of D-altrose and D-galactose H. B-1,3' glycoside of D-altrose and D-galactose
2. Draw the two aldohexoses and one ketohexose that can be derived from the enol shown below. HC OH но H- HO- HO ČH,OH 3. Classify the following monosaccharides as reducing and nonreducing sugars. CH,OH CH,OH CH,OH OH он но - HO- OH OH HO он OH OH ČH,OH II III 4. Identify and name the glycosidic bond in the structure shown below. CH,OH OH OH он
Answer the following questions using the Haworth structure drawn below. Но. CH2 HO, ОН OH ОН a. Identify this monosaccharide. b. Is this the a or ß isomer. c. In solution the cyclic structure above can open and close to form the other isomer. Which structure below is the other isomer that is present in solution? I. II. III. CH2OH O OH CH2OH но -СН, о OH OH OH но CH2 -OH OH ÓH ÓH OH

Chapter 23 Solutions

EP ORGANIC CHEMISTRY -MOD.MASTERING 18W

Ch. 23.4 - Prob. 23.11PCh. 23.5 - Prob. 23.12PCh. 23.5 - Prob. 23.13PCh. 23.6 - Prob. 23.14PCh. 23.6 - Prob. 23.15PCh. 23.7 - Prob. 23.16PCh. 23.7 - Prob. 23.17PCh. 23.7 - Two sugars, A and B, are known to be glucose and...Ch. 23.7 - Prob. 23.19PCh. 23.8 - Prob. 23.20PCh. 23.8 - Prob. 23.21PCh. 23.8 - Prob. 23.22PCh. 23.8 - Prob. 23.23PCh. 23.8 - Prob. 23.24PCh. 23.9 - a. Show the product that results when fructose is...Ch. 23.9 - Prob. 23.26PCh. 23.9 - Prob. 23.27PCh. 23.9 - Prob. 23.28PCh. 23.10 - Prob. 23.29PCh. 23.10 - Prob. 23.30PCh. 23.10 - Prob. 23.31PCh. 23.11 - Prob. 23.32PCh. 23.11 - The Wohl degradation, an alternative to the Ruff...Ch. 23.11 - Prob. 23.34PCh. 23.11 - Prob. 23.35PCh. 23.12A - Prob. 23.36PCh. 23.12A - Give an equation to show the reduction of Tollens...Ch. 23.12A - Prob. 23.38PCh. 23.12B - Prob. 23.39PCh. 23.12C - Prob. 23.40PCh. 23.12C - Prob. 23.41PCh. 23.13A - Prob. 23.42PCh. 23.15 - Cytosine, uracil, and guanine have tautomeric...Ch. 23.15 - a. An aliphatic aminoglycoside is relatively...Ch. 23.16C - Prob. 23.45PCh. 23 - Prob. 23.46SPCh. 23 - Prob. 23.47SPCh. 23 - Prob. 23.48SPCh. 23 - Prob. 23.49SPCh. 23 - Prob. 23.50SPCh. 23 - Prob. 23.51SPCh. 23 - Prob. 23.52SPCh. 23 - Prob. 23.53SPCh. 23 - Prob. 23.54SPCh. 23 - Prob. 23.55SPCh. 23 - Prob. 23.56SPCh. 23 - Prob. 23.57SPCh. 23 - Prob. 23.58SPCh. 23 - Prob. 23.59SPCh. 23 - Prob. 23.60SPCh. 23 - Prob. 23.61SPCh. 23 - Prob. 23.62SPCh. 23 - Prob. 23.63SPCh. 23 - Draw the structure of a four-residue segment of...Ch. 23 - Retroviruses like HIV, the pathogen responsible...Ch. 23 - Prob. 23.66SPCh. 23 - Prob. 23.67SP
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning