36 37 Instructions (questions 36–40): Consider the following reactions. Draw ALL POSSIBLEPRODUCTS, including stereochemistry and/or configuration whenever applicable. Writeyour answer in a piece of paper and then take a photo or scan your answer. Attach theanswer.BrCH,0-37.CH3CH,OH38.CHCH,CH3BrCH339.HO"H-BrČHĄCH3CH340.CH,NH,H,CICH3CHCH3OH41.CH;CH=CHCH,Br 35. Elimination reactions of cis- and trans-1-bromo-2-methylcyclohexanes with NaOEt inELOH can give the same or different main product, 1-methylcyclohexene (1) or 3-methylcyclohexene (2). Which statement indicates the main products?BrBrNaOEINaOEtEIOHEIOHMeMeMe"MecistransA. 1 both from the cis and trans substratesB. 2 both from the cis and trans substratesC. 1 from the cis and 2 from the trans substratesD. 2 from the cis and 1 from the trans substrates36. Which of the following statements regarding regioselectivity of elimination reactionsis wrong?A. More substituted, more stable alkenes are generally formed preferentially byboth E1 and E2 mechanisms.B. Substrates with a poorer nucleophile tend to give the less substituted alkenes.C. Sterically hindered, bulky bases tend to give the less substituted alkenes.D. Reactions by the E1 mechanism are generally less regioselective than thoseby the E2 mechanism.

Answered: Image /qna-images/answer/8bdcbfdf-0484-4731-a067-30578deae724.jpg

Instructions (questions 36–40): Consider the following reactions. Draw ALL POSSIBLE PRODUCTS, including stereochemistry and/or configuration whenever applicable. Write your answer in a piece of paper and then take a photo or scan your answer. Attach the answer. Br CH,0- 37. CH3 CH,OH 38. CHCH,CH3 Br CH3 39. HO" H- Br ČHĄCH3 CH3 40. CH,NH, CH;CH CI

Instructions (questions 36–40): Consider the following reactions. Draw ALL POSSIBLE PRODUCTS, including stereochemistry and/or configuration whenever applicable. Write your answer in a piece of paper and then take a photo or scan your answer. Attach the answer. Br CH,0- 37. CH3 CH,OH 38. CHCH,CH3 Br CH3 39. HO" H- Br ČHĄCH3 CH3 40. CH,NH, CH;CH CI

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.39P: Following are diastereomers (A) and (B) of 3-bromo-3,4-dimethylhexane. On treatment with sodium...

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