i dont want hand writting image OH3. What are the expected major products of these eliminations? Could you use thesame technique as you used in your experiment to isolate these products? Explainyour answers.Amberlyst-15OHAmberlyst-15

You asked for no handwritten structures i hope these are understandable.

Answered: OH 3. What are the expected major…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 35CTQ

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2. Given the following sequence of reactions, draw the structure of products A and B and write a detailed reaction mechanism that explains their formation. H2N H30* A B 3. Write a detailed reaction mechanism for the following transformation. Upload your answer as an attachment. OEt OEt OE
Z. Whch one of the following reagents will not transform an aldehyde to a carboxylic acid? с) Месоон E) HOA9(NH3)2 then H30* D) Zn(Hg), HCI A) CrOs, HSO4 B) KMNO4, H2S04 8. Which one of the following reactions will not produce phenol (PHOH)? PHOCH3 PHOCCH, PhCCHs PhMgBr PhN2* 1) MečoOH H2O Cu,O, H2O 1) LIAIH4 HBr, heat 2) H20, H;O*, heat 2) H2O, H3O* C 9. Which one of the following compounds will not react with F3CC=CCF3 in a Diels-Alder reaction OMe B C 10. Which one of the following compounds is anti-aromatic? HN: : NH A B C 4
Please help with question 38
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
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this drug contains one or more building blocks derived from either ethylene oxide or epichlorohydrin.ldentify the part of each molecule that can be derived from one or the other of the building block and propose structural formulas for the nucleophile(s) that can be used along with either ethylene oxide or epichlorohydrin to synthesize each molecule. Me Me ono Diphenhydramine (Benadryl, an antihistamine)
5. Draw the organic products formed in the following reactions. az vo 2169 snol mo 40-60 g a. b. N [1] LIAIH4 [2] H₂O odior hobnod noitibbs, ogrob [1] Mg Br [2] Å quore [3] H3O+ C. O OH Isprie [1] TBDMS-Cl, imidazole [2] CH3Li [3] H₂O [Indicate stereochemistry.] quong griynol is dit bruggmos lynddisa vesi tuontiv d. of enousNaBH42 OCH3 CH3OH
Q6 Complete the retrosynthetic analysis. Supply all reagents and precursors, for both parts: A and B. Fewest possible reaction paths should be choiun. Part A V Part B Mi
Provide step by step total synthesis of the following target compounds using the starting material provided.

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OH 3. What are the expected major products of these eliminations? Could you use the same technique as you used in your experiment to isolate these products? Explain your answers. Amberlyst-15 OH Amberlyst-15