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

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...

See similar textbooks

Similar questions

Consider the following curved arrow transformations. For each correct transformation draw the result of the movement indicated by the curved arrow. For each incorrect transformation state why the curved arrow is incorrect.
Show all the arrow mechanism including the RIGHT reagents.
Draw a curved arrow mechanism for the reaction to form the major product, adding steps as necessary. Be sure to include all nonzero formal charges. U c+ C + C H A H H + Add/Remove step Click and drag to start drawing a structure.
See the second image for instructions
Please help
d) Circle the compound that would react with HBr the fastest.
Draw a curved arrow mechanism for the reaction. You can assume that all reactants and products are shown.
Draw the Wittig reaction mechanism with arrow pushing.
Draw a reaction coordinate diagram for the reaction. (Hint: An alkyl halide is more stable than an alkene.) Draw the structure of the intermediate/s and their location/s in the above reaction coordinate diagram.
Can you help draw the curved arrow mechanism?
To preview the image for energy diagram click here & Br CH3OH heat A B Energy Energy T Br CH3OH heat Energy Reaction Coordinate Energy Reaction Coordinate Answer the following questions for Reaction A 1. Assign the as SN1, SN2, E1 or E2 [Select] 2. Number of sets of intermediates [Select] 3. Number of transition states [Select] 4. Choose the correct energy diagram [Select] Answer the following questions for Reaction B 5. Assign the as SN1, SN2, E1 or E2 [Select] 6. Number of sets of intermediates [Select] 7. Number of transition states [Select] 8. Choose the correct energy diagram [Select] Reaction Coordinate IV Reaction Coordinate
Provide a stepwise curved arrow mechanism for the following reaction. HO LCH₂CH₂ CH₂CH3 H₂SO4 A CH₂CH3 I CH₂CH3