Organic Chemistry (8th Edition)
Organic Chemistry (8th Edition)
8th Edition
ISBN: 9780134042282
Author: Paula Yurkanis Bruice
Publisher: PEARSON
bartleby

Concept explainers

Question
Book Icon
Chapter 20, Problem 36P

a)

Interpretation Introduction

Interpretation:

An aldopentose that is not D-arabinose and forms D-arabinitol on reduction with NaBH4 is to be identified.

Concept Introduction:

Pentoses are the sugar compounds that belong to five membered monosaccharide units. In the compound of aldopentose an aldehydic functional group is present at the position 1.  D-arabinose is the example of aldopentose.

b)

Interpretation Introduction

Interpretation:

A sugar that is not D-altrose and forms D-altraric acid on oxidation with nitric acid has to be identifed.

Concept Introduction:

D-altrose is a monosaccharide which contains six carbons and aldehyde group.  It exists in D and L forms.  It is formed from dietary lactose.  It is soluble in water but not in methanol.  It is an epimer of mannose sugar.

c)

Interpretation Introduction

Interpretation:

A ketose that is reduced with NaBH4, forms D-altritole and D-allitol has to be identified.

Concept Introduction:

Ketose is a monosaccharide molecule and it contains a ketonic group. Dihydroxyacetone is the simplest ketose molecule with three carbon atoms. NaBH4 is a good reducing agent. It reduces aldehydic group to the alcoholic group in the presence of H3O+.

Blurred answer
Students have asked these similar questions
Identify the sugar in each description. a. An aldopentose that is not d-arabinose forms d-arabinitol when it is reduced with NaBH4. b. A sugar that is not D-altrose forms d-altraric acid when it is oxidized with nitric acid. c. A ketose that, when reduced with NaBH4, forms d-altritol and d-allitol.
Fructose in its bβ - D - pyranose form accounts for the powerful sweetness of honey. The β - D - furanose form, although sweet, is not as sweet as the pyranose form. The furanose form is the more stable form. Draw the two forms and explain why it may not always be wise to cook with honey.
(d) Use the diagram below to complete the cyclic alpha form of structure V (e) Circle the hemiacetal in cyclic alpha form of structure V. (f) Redraw the cyclic alpha form of structure V but replace the OH group on the anomericcarbon with a methoxy group. Is this modified monosaccharide a reducing sugar or anonreducing sugar?

Chapter 20 Solutions

Organic Chemistry (8th Edition)

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
Recommended textbooks for you
Text book image
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
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
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Text book image
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Text book image
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning