3. For each of the following, please propose a synthesis route given the constraints indicateda.starting from any moleculepossessing 2 degrees of unsaturationand no atoms other thancarbon and hydrogenH

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Answered: 3. For each of the following, please…

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter23: Methyl Stearate From Methyl Oleate

Section: Chapter Questions

Problem 2Q

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3) Show a complete mechanism and predict the product for the reaction shown below. Br₂ / H₂O Please provide perspective diagrams (wedge/dash notation), resonance forms, curved arrows, formal charges, and lone pairs as need for all species involved. With reference to the intermediate(s) involved, comment on both the regiochemistry and the stereochemistry of the process.
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Draw the arrows on the structures in the first two boxes to show the mechanism of a-halogenation under basic conditions. All necessary atoms and formal charges are drawn on the structures. See Periodic Table O See Hint H. H. :Br: :Br: 一 Add curved arrow notation to show the reaction between the two compounds. H C P. H. CI H-O: H' :Br: Br :ロ

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3. For each of the following, please propose a synthesis route given the constraints indicated a. starting from any molecule possessing 2 degrees of unsaturation and no atoms other than carbon and hydrogen H