In the problem-solving feature below, methylcyclohexanone was seen to react at its unsubstituted ccarbon. Try to write a mechanism for the same reaction at the methylsubstituted carbon atom, andexplain why this regiochemistry is not observed.CH₂CH₂0-HHOCH3Н.OCH,H.:0:+CH₂CH₂OHDraw all missing reactants, reagents, Intermediates, and/or products inside the appropriateboxes by choosing buttons from the Tools (for bonds and charges), Atoms, and Templatestoolbars.CH₂

The given compound is methyl cyclohexanone which have two acidic site that can be deprotonated by…

stituted a In the problem-solving feature below, methylcyclohexanone was seen to react at its carbon. Try to write a mechanism for the same reaction at the methylsubstituted carbon atom, and explain why this regiochemistry is not observed. H g H CH,CH,O- CH₂ 2 Н. O CH₂ Η. :Ö:¯ + CH₂CH₂OH Draw all missing reactants, reagents, intermediates, and/or products inside the appropriate boxes by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. CH

stituted a In the problem-solving feature below, methylcyclohexanone was seen to react at its carbon. Try to write a mechanism for the same reaction at the methylsubstituted carbon atom, and explain why this regiochemistry is not observed. H g H CH,CH,O- CH₂ 2 Н. O CH₂ Η. :Ö:¯ + CH₂CH₂OH Draw all missing reactants, reagents, intermediates, and/or products inside the appropriate boxes by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. CH

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

Chapter11: Ethers, Epoxides, And Sulfides

Section: Chapter Questions

Problem 11.18P

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