bartleby

Concept explainers

Question
Book Icon
Chapter 21, Problem 35P

(a)

Interpretation Introduction

Interpretation:

The aldopentoses which are enantiomers out of the eight aldopentoses are to be stated.

Concept Introduction:

Enantiomers are the pairs which are mirror images of each other.  These mirror images are non-superimposable to each other.  This means the forms of a compound which exists in two non-superimposable forms each of which is a mirror image of other form is known as enantiomers.

(b)

Interpretation Introduction

Interpretation:

The aldopentoses which are C-2 epimers out of the eight aldopentoses are to be stated.

Concept Introduction:

C-2 epimers are the compounds which has different configuration at second carbon atom and have same configuration at all other carbon atoms.

The stereogenic center present in the compound which makes the orientation of molecules different is known as epimers.

(c)

Interpretation Introduction

Interpretation:

The aldopentoses which forms an optically active compound on oxidation with nitric acid is to be stated.

Concept introduction:

Aldopentoses are the compounds containing five carbon atoms and one aldehyde group at one end of carbon chain which gives dicarboxylic acids called aldaric acids on oxidation with nitric acids.  Aldaric acid is the molecule containing six carbon atoms having carboxylic acid group on both the sides.

Blurred answer
Students have asked these similar questions
6. Match each of the lettered items in the column on the left with the most appropriate numbered item(s) in the column on the right. Some of the numbered items may be used more than once and some not at all. a. Z = 37 1. b. Mn 2. C. Pr element in period 5 and group 14 element in period 5 and group 15 d. S e. [Rn] 7s¹ f. d block metal 3. highest metallic character of all the elements 4. paramagnetic with 5 unpaired electrons 5. 4f36s2 6. isoelectronic with Ca²+ cation 7. an alkaline metal 8. an f-block element
Draw all formal charges on the structures below as is and draw 1 resonance structure that is more stable.
Part II. xiao isolated a compound TAD (Ca H 10 N₂) from tobacco and obtained its IR spectrum. Xiao proposed a chemical structure shown below: % Transmittance 4000 3500 3000 2500 2000 Wavenumber (cm-1) 1500 1000 (a) Explain why her proposed structure is inconsistent with the IR spectrum obtained (b) TAD exists as a tautomer of the structure xiao proposed. Draw the structure and explain why it is more compatible with the obtained spectrum. (C) what is the possible source for the fairly intense signal at 1621cm1

Chapter 21 Solutions

Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th 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
SEE MORE QUESTIONS
Recommended textbooks for you
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
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
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