Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give your route by specifying the number of thestarting material followed by the letters of the reagents you would use beginning with the first step.The answer 4fh means treat t-butanol (4) with conc. HCl(f) then treat the product with KOH in alcohol(h).CH3Starting materialsReagents1BrOHa Mg / dry etherH3COH³4b 1. CO₂ 2. acidic workupc NaCN/THF or DMF2d NaCN/dil. aqueous H₂SO4The most efficient synthetic route isBrBr73g HBrf Conc. HCIOHOHe Ethanol, H₂SO4(trace) at refluxh KOH/alcoholHot8i OsO45Hj Na₂ CrO4 / aqueous H₂SO4요K 1. BH3/THF 2. H₂O₂laq. NaOH

To find out the most efficient synthetic route for the synthesis of p-toluic acid

Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give your route by specifying the number of the starting material followed by the letters of the reagents you would use beginning with the first step. The answer 4fh means treat t-butanol(4) with conc. HCI(f) then treat the product with KOH in alcohol(h). CH₂ Starting materials Reagents Br a Mg/ dry ether H₂C b 1. CO₂ 2. acidic workup c NaCN/THF or DMF "Q d NaCN/ dil. aqueous H₂SO4 The most efficient synthetic route is 7 f Conc. HCI g HBr e Ethanol, H₂SO4 (trace) at reflux OH h KOH/alcohol Hot 4 i OsO4 5 j Na₂ CrO4 / aqueous H₂SO4 k 1. BH/THF 2. H₂O₂/aq. NaOH 1 Å

Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give your route by specifying the number of the starting material followed by the letters of the reagents you would use beginning with the first step. The answer 4fh means treat t-butanol(4) with conc. HCI(f) then treat the product with KOH in alcohol(h). CH₂ Starting materials Reagents Br a Mg/ dry ether H₂C b 1. CO₂ 2. acidic workup c NaCN/THF or DMF "Q d NaCN/ dil. aqueous H₂SO4 The most efficient synthetic route is 7 f Conc. HCI g HBr e Ethanol, H₂SO4 (trace) at reflux OH h KOH/alcohol Hot 4 i OsO4 5 j Na₂ CrO4 / aqueous H₂SO4 k 1. BH/THF 2. H₂O₂/aq. NaOH 1 Å

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

Please don't provide handwriting solution
Draw the product of the following reaction sequence. Ignore any inorganic byproducts formed. H 1. (CH3CH2)2CuLi, THF 2. CH3Br a
Give the major organic product for the following reaction
Propose a strategy for the given synthesis.
Propose a product and an arrow-pushing mechanism for the following reactions.
Identify the reagents you would use to perform the following transformation: Bromocyclohexane →→ Cyclohexanecarboxylic acid The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A. H3O+, heat D. 1) CO2; 2) H3O+ B. Na₂Cr₂O7, H₂SO4, H₂O E. PCC or DMP C. NaCN F. Mg
Write a structural formula for the major product from each of the following reactions. Note: assume that the esters having no a hydrogens are always in excess. Only typed solution and add explanation
This is NOT a graded assignment but please answer with detail and accuracy. Make sure to consider all parts of the problem.
I don't even know how to begin this synthesis. Does the initial attack by the oxygen of the H on the HCl lead to the formation of the OH group in the carboxylic acid or the OH group on the primary alcohol groups?
5. Propose a synthesis of 3-phenylpropanoic acid from diethyl malonate. Show all reactants and reagents.