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...

See similar textbooks

Similar questions

How would you synthesize the following compounds from cyclohexanone using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Reagents a 1. CH3MgBr/dry ether 2 H3O+ e 1. OsO4 i 1. BH3/THF 2. NaHSO3/H2O 2. H₂O₂ / NaOH b 1. C6H5MgBr / dry ether f 1. NaBH4 j Mg / dry ether 2 H3O+ 2. H3O+ с PBr3 g HOCH2CH2OH/HCI k H2/Pd d m-chloroperbenzoic h H3O+ / heat I CrO3 / H3O+ acid m cyclohexanone a) cyclohexylbenzene b) 2-phenylcyclohexanone Submit Answer Try Another Version 3 item attempts remaining
How would you synthesize the following compounds from cyclohexanone using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Reagents a 1. CH3MgBr / dry ether 2 H3O+ e 1. OsO4 i 1. BH3/THF 2. NaHSO3/H₂O 2. H₂O₂ / NaOH b 1. C6H5 MgBr / dry ether f 1. NaBH4 j Mg / dry ether 2 H3O+ 2. H3O+ C PBг3 g HOCH2CH2OH/HCI k H2/Pd d m-chloroperbenzoic h H3O+ / heat 1 CrO3 / H3O+ acid a) 2-phenylcyclohexanone b) cyclohexylbenzene m cyclohexanone
How would you synthesize the following substances from benzaldehyde and reagents from the table? In general, the fewer the steps, the better the synthesis. You should not need more than four steps. Use letters from the table to list reagents in the order used (first at the left) with no commas. Example: cag Reagents a CH2=0 f 1. CH3MgBr / dry ether 2 H3O+ j 1. P(C6H5)3 2. BuLi b O g Dess-Martin periodinane KA Br2 in CH2Cl2 C (C6H5)3P+-CH2 h 1. NaBH4 1. PBг3 2. H3O+ d m NH + acid i 1. BH3/THF NaNH2/NH3 2. H2O2 / NaOH e CrO3/H3O+ n Mg/ dry ether a) Previous Next
Ethers/Aldehydes/Ketones SynthesisPrepare the following compounds from any simple alkyl halide having four carbons or less,cyclohexane, and/or benzene. You may also use ethylene oxide (oxacyclopropane). SHOW ALLSTEPS AND REAGENTS with arrows.
Draw mechanisms for the following reactions. Use curved arrows to show electron flow for each step and draw out all reactants to effectively show all arrow pushing. Write a written description of the mechanisms.
2. Propose a synthesis of the molecule below using benzene and carboxylic acids of three carbons or fewer (note: an acyl halide is NOT a carboxylic acid) as your source of carbon atoms. You may use any inorganic reagent needed to complete your synthesis. Clearly show each synthetic step. Do not show curved arrow mechanisms.
Using your reaction roadmap as a guide, show reagents and conditions to bring about these conversions, which may require more than one step.
What is a suitable synthesis to complete the transformation below? Show all steps with reagents and products.
How would you prepare the product from the given starting material? Show the retrosynthetic analysis. Show all reaction steps and give reagents. You do not need to show intermediates or mechanisms. The number of arrows does not indicate the number of steps, but just indicate that there are multiple steps. Make sure to show the retrosynthetic analysis and the reaction steps (label which is the analysis and which are the steps. 1.) HC *triple bond* CCH2CH3 -----> CH3CH2*C*HCH2Br ------> ------> *substiuent of (Br) on the starred carbon on right side equation
Show how to synthesize the following product as the major product starting with 2,2-dimethylpropane as the starting material. You may use additional reagents and any number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions). Write the process.
Starting from cyclohexanol, show how to prepare: OMe (racemic) "OMe Show all reagents and molecules synthesized along the way after each step. You do not have to use curved arrows.
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

SEE MORE QUESTIONS

Recommended textbooks for you

Chemistry

ISBN:

9781305957404

Author:

Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:

Cengage Learning

Chemistry

ISBN:

9781259911156

Author:

Raymond Chang Dr., Jason Overby Professor

Publisher:

McGraw-Hill Education

Principles of Instrumental Analysis

Chemistry

ISBN:

9781305577213

Author:

Douglas A. Skoog, F. James Holler, Stanley R. Crouch

Publisher:

Cengage Learning

Chemistry

ISBN:

9781305957404

Author:

Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:

Cengage Learning

Chemistry

ISBN:

9781259911156

Author:

Raymond Chang Dr., Jason Overby Professor

Publisher:

McGraw-Hill Education

Principles of Instrumental Analysis

Chemistry

ISBN:

9781305577213

Author:

Douglas A. Skoog, F. James Holler, Stanley R. Crouch

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9780078021558

Author:

Janice Gorzynski Smith Dr.

Publisher:

McGraw-Hill Education

Chemistry: Principles and Reactions

Chemistry

ISBN:

9781305079373

Author:

William L. Masterton, Cecile N. Hurley

Publisher:

Cengage Learning

Elementary Principles of Chemical Processes, Bind…

Chemistry

ISBN:

9781118431221

Author:

Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard

Publisher:

WILEY

SEE MORE TEXTBOOKS