H3C- OH ACO H -H CH3 H H Aco Ac H3C - OAC Dess-Martin periodinane provides a means to oxidize a primary alcohol to aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be recovered. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions 000 XT H3C 'Н AAQ H H3C OH H3C OAc чь
H3C- OH ACO H -H CH3 H H Aco Ac H3C - OAC Dess-Martin periodinane provides a means to oxidize a primary alcohol to aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be recovered. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions 000 XT H3C 'Н AAQ H H3C OH H3C OAc чь
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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Question
![OH
oth
-H
H
H3C-
NX
XT
OAc
ACO
-OAc
&
O
Dess-Martin periodinane provides a means to oxidize a primary alcohol to an aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2
elimination, whereby a C=O double bond is formed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be
recovered.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
H3C
CH3
H
ACO
$$
H
H3C
H3C
H
:0:
H H3C
OH
OAC
чь](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F98300f68-cb9e-4c94-97bf-c558b3a74855%2F34109368-b051-4a64-875a-134697b6233b%2F10gtmh_processed.jpeg&w=3840&q=75)
Transcribed Image Text:OH
oth
-H
H
H3C-
NX
XT
OAc
ACO
-OAc
&
O
Dess-Martin periodinane provides a means to oxidize a primary alcohol to an aldehyde, while avoiding the use of toxic Cr(VI) compounds. The mechanism involves a reaction similar to the E2
elimination, whereby a C=O double bond is formed with a reduced iodine compound as the leaving group. The reaction occurs in a nonaqueous solvent, CH₂Cl₂, so that the aldehyde product can be
recovered.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
H3C
CH3
H
ACO
$$
H
H3C
H3C
H
:0:
H H3C
OH
OAC
чь
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