3. Perform a retrosynthetic analysis on the followingalkene. Show both ways of making it from alkylhalides and carbonyl compounds. After you haveshown both syntheses, suggest which of the twowould be a better one. Show both startingmaterial combinations with your model kit andshare pictures. Using the model kit will help youwith getting the answer.

Step 1: There are two alternative sets of reactants that we can use to begin the synthesis of the…

Answered: 3. Perform a retrosynthetic analysis on…

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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First, identify a synthetic route for the production of 1-butyne from acetylene. 1st 2nd reagents reagents H -H Br The transformations above can be performed with some combination of the reagents listed below. Give the necessary reagents in the correct order for each transformation, 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 B с Mel Br2₂, hv E F H₂, Lindlar's cat. HBr H HBr, ROOR H₂, Pt Br D HC=CNa G NaNH, 1st reagents: 2nd reagents:
Propose an efficient synthesis for the following transformation: 1-butyne to trans-3,4-dibromohexaneThe transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) 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 B C Br2 NaNH2 Na, NH3 (l) D E F dilute H2SO4 H2, Lindlar's catalyst MeI G H I 1) BH3·THF2) H2O2, H2O 1) xs NaNH22) H2O
Draw compound A and B and identify reagents 1,2 and 3
Design two syntheses of the compound below using the Wittig reagent and a carbonyl compound. Show all reagents and intermediates . Of the two , which is the better synthesis . Explain your reasoning
7. Show the reagents that would be necessary to carry out each transformation and any major products that would be formed in the intermediate stages. (You may have to use reactions from the last test material) 2-methylpropane 2-methylpropene
12. Provide a pathway to make the given carboxylic acid from the given starting material. Give all the reagents and write out the reactions. Show mechanism. OH & Br OH COOH
1. Show the steps necessary to make this compound using a Wittig reaction. Start with triphenylphosphine and an alkyl halide. After that you may use any other organic or inorganic reagents CH₂
References) Work out this synthesis of para-nitrobenzoic acid using the same retrosynthetic approach. O= O C-OH NO₂ Propose a possible final step for your synthesis. This step must lead directly from a synthetic intermediate to the final product_ Select one of these possible synthetic intermediates, then select a reagent. Intermediate: CH3 para-nitrobenzoic acid NO₂ para-nitrotoluene NO₂ nitrobenzene C-OH benzoic acid
Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: OEt CI & NO₂ The target molecule above can be prepared by treating benzene 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 1) EtMgBr 2) H₂O¹ D NaOEt, heat B HNO₂, H₂SO4 E NaOH, heat C D F Cl₂, AICI CH-CH₂COCI, AICI
Please help with both questions. Thanks!
Draw an alkyl bromide that would produce ONLY the following alkene in an E2 elimination. Ignore any inorganic byproducts.
Show step by step reactions with proper reagents how you would carry out the following chemical conversion.

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