Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
Question
Book Icon
Chapter 6, Problem 44P
Interpretation Introduction

Interpretation:

The reactions of the Walden cycle likely to take place with the overall inversion of configuration and those likely to occur with the overall retention of the configuration are to be determined. The configurations of the other compounds in the Walden cycle are to be determined. The Walden cycle, based on the use of thionyl chloride instead of PCl5, is to be written.

Concept introduction:

Reaction sequences involve the conversion of one functional group to another, which may also require the addition or loss of carbon from the reactant.

These sequences involve a number of steps carried out by different reagents. Sometimes, different reagents give the same products.

Electrophiles are electron-deficient species, which has positive or partially positive charge. Lewis acids are electrophiles, which accept electron pair.

Nucleophiles are electron-rich species, which has negative or partially negative charge. Lewis bases are nucleophiles, which donate electron pair.

Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a functional group is substituted by any other functional group is called substitution reaction.

Nucleophilic substitution reaction is a reaction in which an electron-rich nucleophile attacks the positive or partial positive charge of an atom or a group of atoms to replace a leaving group.

An SN2 reaction is the nucleophilic substitution reaction in which two components are involved in the rate determining step. SN2 reaction occurs in one step.

An SN1 reaction is the nucleophilic substitution reaction in which one component is involved in the rate determining step. SN1 reaction occurs in two step.

The involvement of nearby nucleophile substituent to the reaction center in the substitution process is known as neighboring group participation.

Such participation results in an increase of rate of reaction. The phenomenon is described as Anchimeric assistance.

In this participation, two SN2 reactions are occurred, which results in two inversion of configuration, that is, overall retention of configuration.

When the order of progression from the group of highest priority to that of the next highest priority is clockwise, it is said to be the (R) configuration

When the order of progression from the group of highest priority to that of the next highest priority is anticlockwise, then it is said to be the (S) configuration.

Blurred answer
Students have asked these similar questions
The longest wavelength electronic transition in simple unsaturated hydrocarbons corresponds to a transition from the highest occupied molecular orbita l (HOMO) to the lowest unoccupied molecular orbita l (LUMO) . Predict the energy of the HOMO to LUMO separation in (a) ethane. (b) butadiene. and (c) benzene.
What types of electronic transitions are possible for each of the following compounds?(a) Cyclopentene(b) Acetaldehyde(c) Dimethyl ether(d) Methyl vinyl ether(e) Triethylamine(f) Cyclohexane
(a) Determine the absolute configurations of the reactant and the product... (b) What does "retention of configuration" mean?
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    EBK A SMALL SCALE APPROACH TO ORGANIC L
    Chemistry
    ISBN:9781305446021
    Author:Lampman
    Publisher:CENGAGE LEARNING - CONSIGNMENT
    Text book image
    Chemistry
    Chemistry
    ISBN:9781305957404
    Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
    Publisher:Cengage Learning
  • Text book image
    Chemistry: An Atoms First Approach
    Chemistry
    ISBN:9781305079243
    Author:Steven S. Zumdahl, Susan A. Zumdahl
    Publisher:Cengage Learning
    Text book image
    Chemistry
    Chemistry
    ISBN:9781133611097
    Author:Steven S. Zumdahl
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781133611097
Author:Steven S. Zumdahl
Publisher:Cengage Learning