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(30 Chapter 16: Oxidation of Aromie Compounds 0 Oxidation of Alkyl - CH₂ CH3 2 CH3 CUL 1 Кмпон, H₂O Side chains COOH

(30 Chapter 16: Oxidation of Aromie Compounds 0 Oxidation of Alkyl - CH₂ CH3 2 CH3 CUL 1 Кмпон, H₂O Side chains COOH

Chemistry
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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Need details / shows mechanism of how COOH form from CH2CH3 after KMnO4 is added

(30) Chapter 16: Oxidation of Aromatic •Compounds Oxidation Ет снасна CH3 CH3 (2 When an the side chain - H H уча of Alkyl Side CH3 CH3 Bromination of Alkyl benzene treated is alkyl ben zene at the benzylic position occurs. H₁Br Mechanism: N-Br O (Ph CO2)2 benzoyl peroxide CCL4 KMnO4 H₂O bromination KMnO4, NR H₂O CH3 Br Br chains CH 3 + -COOH Side Chains with CH3 HBr N-bromo succinimide (NBS), Br H poth e Br 2 + -CH3 N-H reaction
Transcribed Image Text:(30) Chapter 16: Oxidation of Aromatic •Compounds Oxidation Ет снасна CH3 CH3 (2 When an the side chain - H H уча of Alkyl Side CH3 CH3 Bromination of Alkyl benzene treated is alkyl ben zene at the benzylic position occurs. H₁Br Mechanism: N-Br O (Ph CO2)2 benzoyl peroxide CCL4 KMnO4 H₂O bromination KMnO4, NR H₂O CH3 Br Br chains CH 3 + -COOH Side Chains with CH3 HBr N-bromo succinimide (NBS), Br H poth e Br 2 + -CH3 N-H reaction
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