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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 CH3CI HCI + 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 Br:/FeBr3 Mg Br Mg HO. Br ether p-Bromotoluene phenylmagnesium bromide acetic acid Scheme 3. Bromo 1 methyl benzene forms Grignard reagent upon reacting magnesium KMN04 HO он HO acetic acid Terephthalic acid Scheme 4. Bromo 1 methyl benzoic acid umdergo oxidation in presence of potassium permanganate to form COOH and we get the desired acid (Terephthalic acid) O=

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 CH3CI HCI + 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 Br:/FeBr3 Mg Br Mg HO. Br ether p-Bromotoluene phenylmagnesium bromide acetic acid Scheme 3. Bromo 1 methyl benzene forms Grignard reagent upon reacting magnesium KMN04 HO он HO acetic acid Terephthalic acid Scheme 4. Bromo 1 methyl benzoic acid umdergo oxidation in presence of potassium permanganate to form COOH and we get the desired acid (Terephthalic acid) O=

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 Br:/FeBr3 Mg Br Mg HO. Br ether p-Bromotoluene phenylmagnesium bromide acetic acid Scheme 3. Bromo 1 methyl benzene forms Grignard reagent upon reacting magnesium KMN04 но 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 Br:/FeBr3 Mg Br Mg HO. Br ether p-Bromotoluene phenylmagnesium bromide acetic acid Scheme 3. Bromo 1 methyl benzene forms Grignard reagent upon reacting magnesium KMN04 но 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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