Heating the following molecule in ethanol gave a major product with molecular formula C,H12 ,which when treated with O3 followed by Me2S produced the diketone shown.BrCH3CH,OH1. O3C,H12heat2. Me,S(i)Deduce the structure of the product with molecular formula C,H12 from theinformation provided. Write an arrow formalism reaction mechanism to show howthe compound with molecular formula C,H12 is formed.(ii)How would you perform the following transformation to obtain the final product asthe MAJOR product. More than one step is needed. Show all the steps in yoursynthesis. Reaction mechanisms are not required.Brmore than one stepless than four stepsOHCCHO

This is an Elimination reaction based on E1 and E2 mechanism. See the complete detailed solution…

Heating the following molecule in ethanol gave a major product with molecular formula C;H12 , which when treated with O3 followed by Me2S produced the diketone shown. Br CH3CH,OH 1. O3 C,H12 heat 2. Me,S (i) Deduce the structure of the product with molecular formula C,H12 from the information provided. Write an arrow formalism reaction mechanism to show how

Heating the following molecule in ethanol gave a major product with molecular formula C;H12 , which when treated with O3 followed by Me2S produced the diketone shown. Br CH3CH,OH 1. O3 C,H12 heat 2. Me,S (i) Deduce the structure of the product with molecular formula C,H12 from the information provided. Write an arrow formalism reaction mechanism to show how

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 33MP

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