pls solve this problem with in 1 hour. Explain it also ChemistryCurrent Attempt in ProgressIdentify the reagents that can be used to accomplish the following transformationOHThe transformation above can be performed with some reagent or combination of the reagents isted below. Givethe necessaryreagents in the correct order, as a string of letters (without spaces or punctuation. such an EBF) there is more than one corredsolution, provide just one answer.A 1) Br, NaOH: 2) HOB. Na,CryO, HSO HOC.1)O 2) DMSD. PCC or DMPE 1) CO; 2) H,O"F. ELOH, H;SO,eTextbook and MediaAttempts: O of 3 used Subnit

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Current Attempt in Progress Identity the reagents that can be uned to accomplish the following tranornation OH The transformation above can be performed with some reagent or combination of the reagents ted below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation sachn EOF there is more than one core solution, provide just one answer. B. NaCrO, HSO H0 E1) CO, 2) HO A 1) Br, NaOH 2) H0 C1O 2 DMS F.EIOH.H,SO, D. PCC or DMP eTextbook and Media

Current Attempt in Progress Identity the reagents that can be uned to accomplish the following tranornation OH The transformation above can be performed with some reagent or combination of the reagents ted below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation sachn EOF there is more than one core solution, provide just one answer. B. NaCrO, HSO H0 E1) CO, 2) HO A 1) Br, NaOH 2) H0 C1O 2 DMS F.EIOH.H,SO, D. PCC or DMP eTextbook and Media

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations

Section11.SE: Something Extra

Problem 43AP

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11.1 Synthesis. Show by a series of steps how you could synthesize the following compounds from the given starting compound: Show the step-by-step process. Do not use shortcut methods. Make it as detailed as it can be. Encode (not hand-written)!
Propose an efficient synthesis for the following transformation: 1-butyne to 2-butanolThe 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 1) O32) DMS 1) xs NaNH22) H2O 1) BH3·THF2) H2O2, H2O D E F dilute H2SO4 H2, Lindlar's catalyst Br2
Which of the following reagent best accomplish this transformation below? a. Li/NH3 b. H2SO4, H2O, HgSO4 c. BH3, THF d. potassium permanganate
gas, Cl¬CH2CH2¬S¬CH2CH2¬Cl, was used as a poisonous chemical agentin World War I. Mustard gas is much more toxic than a typical primary alkyl chloride. Itstoxicity stems from its ability to alkylate amino groups on important metabolic enzymes,rendering the enzymes inactive.(a) Propose a mechanism to explain why mustard gas is an exceptionally potent alkylatingagent.(b) Bleach (sodium hypochlorite, NaOCl, a strong oxidizing agent) neutralizes and inactivates mustard gas. Bleach is also effective on organic stains because it oxidizes coloredcompounds to colorless compounds. Propose products that might be formed by thereaction of mustard gas with bleach.
From the table of available reagents select the one(s) you would use to accomplish the transformations shown below.
1. Using a Lewis acid, BF3, (+) aureal (1) undergoes a rearrangement Org. Lett 2012, 14, 4710-4713. Using arrows propose a mechanism for this rearrangement. 2. Explain why we added BF3 as an acid to the alcohol? How does it help with reaction ( 3 --> 4)? 3. What is the process’ name for (4) --> (5)? 4. going from (5) to (6)? 5. from (6) to (2)?
Choose the best reagents to complete the following reaction. There's another answer choice not shown on screen: E) 1. CH3Li 2. H3O+ Hint: The correct answer is not option C.
7. Roadmap. Complete the following roadmap synthesis by providing all the missing reagents. If more than one step is required, be sure to indicate so with sequential steps. No sequence should be more than 3 steps.
Please give a detailed stepwise mechanism for the following reactions of Q.1 and Q.2. All arrows, charges, intermediates, and resonance structures must be shown.
Select the necessary reagent(s) for the following transformation.The answer is NOT Cu^2+ a. H+/H2O b. K2Cr2O7 c. NaOH d. H2/Pt e. Cu^2+ f. I2
We now continue the introduction of organic chemistry reaction roadmaps. Because of the many new functional groups that will be introduced in coming chapters, we recommend that you make a new roadmap to accommodate the reactions in Chapters 1518. To make your own reaction roadmap for Chapters 1518, take a blank sheet of paper and write the following functional groups in the orientations shown. Fill the entire sheet of paper and leave plenty of room between functional groups. Most students find it helpful to use a poster-sized piece of paper filled out in landscape orientation. Refer to the Study Guide section of this chapter. Draw arrows between functional groups to account for each reaction. Write the reagents required to bring about each reaction next to the arrow. Then record any regiochemistry or stereochemistry considerations relevant to the reaction. You should also record any key aspects of the mechanism, such as formation of a carbocation intermediate, as a helpful reminder. It is important to keep track of all reactions that make carbon-carbon bonds, because these will help you build large molecules from smaller fragments. On the above organic chemistry reaction roadmap template, the information for the Simmons-Smith reaction, the seventh reaction in the Study Guide section has been added to help you get started. For this reaction roadmap, do not write an arrow for reactions 1, 2, and 4 explicitly, because these are considered reagents, which are prepared immediately prior to use. A reaction roadmap is used to indicate interconversion of molecules with more stable functional groups. Appendix 10 contains a series of roadmaps for different sections of the book, but you should use those for reference only after you have completed your own.
4) Aromatic compounds are among the most abundant and versatile in nature. From a synthetic point of view, these compounds, despite their stabilities, are quite useful and can undergo reactions under special conditions and by specific mechanisms, such as the Electrophilic Aromatic Substitution (SAE) and the Nucleophilic Aromatic Substitution (SNAr). Based on this, please answer the following items: (b) How would you prepare the following compounds starting from benzene? Explain the second in a different way