Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, showyour retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents.Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply.OOH1) TsCl, pyridine2) NaOEt1) TsCl, pyridine2) I-BuOKOHCINaOHRaобOHCIt-BuOKconc. H₂SO4heatCIt-BuOK

Step 1: Mechanism Step 2: Reaction 2E1 elimination process.Conversion of the OH group into a more…

Answered: Provide a synthesis for the target…

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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Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents. Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. U U U 3 Br Br t-BUOK OH Br t-BuOK NaOH LOH conc. H₂SO4 heat Br NaOEt conc. H₂SO4 heat
Make a systematic process for the synthesis of the benzene derivative from benzene. Present all the needed reagent and reaction conditions and products. (Note the electron-donating or electron- withdrawing) NH2
Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents. Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. ☐ ☐ Br HO Br HO Br HO t-BUOK conc. H₂SO4 heat NaOH 1) TSCI, pyridine 2) NaOH NaOH t-BUOK 1) TSCI, pyridine 2) t-BUOK
7) Using the carbon-containing starting material(s), propose a synthesis the following retrosynthetic analysis. Provide structures for all intermediates. The carbon atoms in the product must originate from the starting material(s), but you may use as many equivalents of each starting material as you would like, and any reagent/reaction you know (note: no mechanisms are required). Br OH racemic = = + -Br
Propose a sequence of reactions to prepare the specified target compound from the indicated starting materials. All of the carbon atoms in the target must originate in the specified starting materials. Keeping this restriction in mind, you may use any other organic or inorganic reagents necessary to complete the synthesis. It is only necessary to show the overall transformations involved in your proposed synthesis.
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
Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: CI * Incorrect. COOH A Br 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. ECABF D NO₂ 1) KMnO4, NaOH, heat 2) H3O+ HNO3, H₂SO4 B E 1) CO2 2) H3O+ (CH3)2CHCI, AICI 3 с Br2, AlBr3 F Cl2, AICI 3
Provide a synthesis for each of the following reactions using reagents containing no more than 4 carbon atoms. Show each intermediate structure between steps. No arrow-pushing mechanisms are required. -ox OH OH

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