Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the mechanism. CH3CH3MsCIOMsoccurs. The resulting sulfonate esters are reactive in Syi and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving groupDraw curved arrows to show the movement of electrons in this step of the mechanism.Arrow-pushing InstructionsAlcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configurationCH3 :00:CH3:CI:CH3он

Here we need to show the electron movement in the following reaction:

Answered: CH3 CH3 MsCI OMs occurs. The resulting…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.

Draw curved arrows to show the movement of electrons in this step of the mechanism.

CH3
CH3
MsCI
OMs
occurs. The resulting sulfonate esters are reactive in Syi and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration
CH3 :0
0:
CH3
:CI:
CH3
он

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