OsPE2. Predict the products and draw the mechanism of the reaction below showing any relevant transitionstates. Additionally, name the reactant and the product properly indicating stereochemistry.CM₂AC43BrCM₂Connen &NaOEtDMSONo. o Et(15,25)-1-bromo-2-methyl cyclohexave&сну2CHA(S)-3-vethyl cyclohexiene3. Changing the conditions of the reaction in the previous question to an ethanol solvent gives severalproducts in addition to the one predicted above. Draw these products.447 --- E+0transition stateHydride shiftJсизиCHEM 241-Group09. Ormord**3

Answered: Image /qna-images/answer/644f92fd-2b58-4357-b22b-6c7c2121bd6d.jpg

2. Predict the products and draw the mechanism of the reaction below showing any relevant transition states. Additionally, name the reactant and the product properly indicating stereochemistry. S Br NaOEt DMSO No.02t> [O CIS Dr 4E+0 transition state -> сиз (3)-3-methyl cyclohexene 125)-1-Lramo-2-methyl cyclohexame 3. Changing the conditions of the reaction in the previous question to an ethanol solvent gives several products in addition to the one predicted above. Draw these products.

2. Predict the products and draw the mechanism of the reaction below showing any relevant transition states. Additionally, name the reactant and the product properly indicating stereochemistry. S Br NaOEt DMSO No.02t> [O CIS Dr 4E+0 transition state -> сиз (3)-3-methyl cyclohexene 125)-1-Lramo-2-methyl cyclohexame 3. Changing the conditions of the reaction in the previous question to an ethanol solvent gives several products in addition to the one predicted above. Draw these products.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter30: Orbitals And Organic Chemistry: Pericyclic Reactions

Section30.SE: Something Extra

Problem 36AP

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