CH3གོན་ནི། ཡོན་Br₂,H₂CCH₂BrH3C CH3H₂C CH3Aldehydes and ketones can be halogenated at their a-position by reaction with Cl₂, Br2, or 12, under acidic conditions. Using Br₂ under acidic conditions, an intermediate enol is formed which addsbromine at the a-position. The reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation lessfavorable.Draw curved arrows to show the movement of electrons in this step of the mechanism.Arrow-pushing Instructions:0::OHн-онH-OH₂H₂OH₂C.H3C.CH3CH3H3C CH3H3C CH3Σα

The objective of this question is to draw the curved arrows to show the movement of electrons in the…

Answered: Draw curved arrows to show the movement…

Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions :OH :0: HOH, H₂O H3C. H3C CH3 CH3 H3C CH3 H3C CH3

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

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CH3
གོན་ནི། ཡོན་
Br₂,
H₂C
CH₂Br
H3C CH3
H₂C CH3
Aldehydes and ketones can be halogenated at their a-position by reaction with Cl₂, Br2, or 12, under acidic conditions. Using Br₂ under acidic conditions, an intermediate enol is formed which adds
bromine at the a-position. The reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation less
favorable.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
:0:
:OH
н-он
H-OH₂
H₂O
H₂C.
H3C.
CH3
CH3
H3C CH3
H3C CH3
Σα

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