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Below, depicts the electron flow process for the synthetic schemes. This should include the prediction of significant and by-products through electronic and structural impacts. The mechanism for pushing the arrow must be shown.

Below, depicts the electron flow process for the synthetic schemes. This should include the prediction of significant and by-products through electronic and structural impacts. The mechanism for pushing the arrow must be shown.

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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Below, depicts the electron flow process for the synthetic schemes. This should include the prediction of significant and by-products through electronic and structural impacts. The mechanism for pushing the arrow must be shown. SYNTHESIS OF TEREPHTALIC ACID AICI3 HCI CH3CI + + toluene Scheme 1. Formation of Toluene using Friedel Craft Alkylation Br2 FeBr3 Br Br toluene o-Bromotoluene p-Bromotoluene Scheme 2. Bromination of Toluene using Br2/FeBr3 of Mg C: Br `Mg Br ether p-Bromotoluene phenylmagnesium bromide acetic acid Scheme 3. Bromo 1 methyl benzene forms Grignard reagent upon reacting magnesium KMN04 HO HO. HO acetic acid Terephthalic acid Scheme 4. Bromo 1 methyl benzoic acid undergo oxidation in presence of potassium permanganate to form COOH and we get the desired acid (Terephthalic acid)
Transcribed Image Text:Below, depicts the electron flow process for the synthetic schemes. This should include the prediction of significant and by-products through electronic and structural impacts. The mechanism for pushing the arrow must be shown. SYNTHESIS OF TEREPHTALIC ACID AICI3 HCI CH3CI + + toluene Scheme 1. Formation of Toluene using Friedel Craft Alkylation Br2 FeBr3 Br Br toluene o-Bromotoluene p-Bromotoluene Scheme 2. Bromination of Toluene using Br2/FeBr3 of Mg C: Br `Mg Br ether p-Bromotoluene phenylmagnesium bromide acetic acid Scheme 3. Bromo 1 methyl benzene forms Grignard reagent upon reacting magnesium KMN04 HO HO. HO acetic acid Terephthalic acid Scheme 4. Bromo 1 methyl benzoic acid undergo oxidation in presence of potassium permanganate to form COOH and we get the desired acid (Terephthalic acid)
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