Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
bartleby

Concept explainers

Question
Book Icon
Chapter 22, Problem 23P
Interpretation Introduction

Interpretation:

The reason for the fact that d-mannose can exist as dextrorotatory as well as levorotatory is to be explained.

Concept introduction:

By convention, the terms dextrorotation and levorotation (or laevorotation) represent the movement of plane polarized light clockwise or anticlockwise, respectively, for a compound as seen by the observer whom the light is approaching. The compound exhibiting dextrorotation is said to be dextrorotatory and that exhibiting levorotation is said to be levorotatory.

The dextrorotation and levorotation can be quantized by measuring the degree of specific rotation of the compound, α, which can be given as;

[α]=αc×l, where α is the observed rotation (in degrees)                    c is the concentration of the solution of an enatiomer (in g/mL)                    and l is the length of the polarimeter tube (in decimeters)   

The value of dextrorotation is positive (+) and that of levorotation is negative (-).

Blurred answer
Students have asked these similar questions
d-Xylose and d-lyxose are formed when d-threose undergoes a Kiliani–Fischer synthesis. d-Xylose is oxidized to an optically inactive aldaric acid,whereas d-lyxose forms an optically active aldaric acid. What are the structures of d-xylose and d-lyxose?
The 1H NMR spectrum of d-glucose in D2O exhibits two high-frequency doublets. What is responsible for these doublets?
The following observations are obtained after a D-hexose was made to react with several reagents: (1) The reactions of a D-hexose with (a) to (d) below yields an aldaric acid (a) NH₂OH, (b) (CH3CO)₂O, NaOCOCH 3, and, (c) NaOCH3, and then, (d) HNO3, H₂O (2) HNO3 oxidation of the same D-hexose gives an aldaric acid. Predict the structures of the three (3) possible hexoses that can undergo the above reactions?
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
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
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Brooks Cole
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
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning