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The reaction below proceeds with the formation of four (4) products. Choose the mechanism below which best describes the following transformation. : OH Mechanism A: : OH proton transfer H-CI: ☆ Mechanism B: (:OH CH3 : OH loss of a leaving group methyl migration (rearrangement) Mechanism C: :OH Mechanism D: :OH ✓: OH₂ H-CI: proton transfer X :CB loss of a leaving group HCI O CH3 Do Ⓒ. : OH₂ loss of a leaving group - H₂O :CI e :CI: Ⓒ.. : OH nucleophilic attack :CI CH₂ O :CI: nucleophilic attack secondary carbocation nucleophilic attack :CI secondary carbocation methyl migration (rearrangement) tertiary carbocation nucleophilic attack $-$$ ✪. : OH₂ CH₂ nucleophilic attack methyl migration (rearrangement) CH3 e methyl migration (rearrangement) :CI CH3 tertiary carbocation A tertiary carbocation :CI: Ⓒ.. OH₂ O CH₂ CH₂ CH3 CH₂ resonance - H₂O loss of a leaving group CH₂ + secondary carbocation resonance + secondary carbocation - H₂O methyl migration (rearrangement) CH₂ CH3 CH₂ CH3 loss of a leaving group C ل

The reaction below proceeds with the formation of four (4) products. Choose the mechanism below which best describes the following transformation. : OH Mechanism A: : OH proton transfer H-CI: ☆ Mechanism B: (:OH CH3 : OH loss of a leaving group methyl migration (rearrangement) Mechanism C: :OH Mechanism D: :OH ✓: OH₂ H-CI: proton transfer X :CB loss of a leaving group HCI O CH3 Do Ⓒ. : OH₂ loss of a leaving group - H₂O :CI e :CI: Ⓒ.. : OH nucleophilic attack :CI CH₂ O :CI: nucleophilic attack secondary carbocation nucleophilic attack :CI secondary carbocation methyl migration (rearrangement) tertiary carbocation nucleophilic attack $-$$ ✪. : OH₂ CH₂ nucleophilic attack methyl migration (rearrangement) CH3 e methyl migration (rearrangement) :CI CH3 tertiary carbocation A tertiary carbocation :CI: Ⓒ.. OH₂ O CH₂ CH₂ CH3 CH₂ resonance - H₂O loss of a leaving group CH₂ + secondary carbocation resonance + secondary carbocation - H₂O methyl migration (rearrangement) CH₂ CH3 CH₂ CH3 loss of a leaving group C ل

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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The reaction below proceeds with the formation of four (4) products. Choose the mechanism below which best describes the following transformation. : OH Mechanism A: : OH proton transfer Mechanism B: (:OH H-CI: methyl migration (rearrangement) CH3 Mechanism C: : OH loss of a leaving group OA OB OC OD Mechanism D: :OH proton transfer :OH ✓: OH₂ Ex :CB loss of a leaving group H-CI: HCI O CH3 loss of a leaving group - H₂O CH₂ CH3 & & & में + + :CI secondary carbocation Ⓒ. Dis ģ : OH₂ e :CI: Ⓒ.. : OH $. &&& nucleophilic attack CH₂ secondary carbocation nucleophilic attack :CI nucleophilic attack $-$$ O :CI: nucleophilic attack :CI secondary carbocation methyl migration (rearrangement) tertiary carbocation methyl migration (rearrangement) CH3 CH₂ nucleophilic attack : OH₂ e methyl migration (rearrangement) CH3 tertiary carbocation A tertiary carbocation :CI: $.$ :CI Ⓒ.. OH₂ O CH₂ CH₂ CH3 resonance CH₂ - H₂O loss of a leaving group resonance secondary carbocation CH₂ CH3 - H₂O methyl migration (rearrangement) CH₂ loss of a leaving group - &
Transcribed Image Text:The reaction below proceeds with the formation of four (4) products. Choose the mechanism below which best describes the following transformation. : OH Mechanism A: : OH proton transfer Mechanism B: (:OH H-CI: methyl migration (rearrangement) CH3 Mechanism C: : OH loss of a leaving group OA OB OC OD Mechanism D: :OH proton transfer :OH ✓: OH₂ Ex :CB loss of a leaving group H-CI: HCI O CH3 loss of a leaving group - H₂O CH₂ CH3 & & & में + + :CI secondary carbocation Ⓒ. Dis ģ : OH₂ e :CI: Ⓒ.. : OH $. &&& nucleophilic attack CH₂ secondary carbocation nucleophilic attack :CI nucleophilic attack $-$$ O :CI: nucleophilic attack :CI secondary carbocation methyl migration (rearrangement) tertiary carbocation methyl migration (rearrangement) CH3 CH₂ nucleophilic attack : OH₂ e methyl migration (rearrangement) CH3 tertiary carbocation A tertiary carbocation :CI: $.$ :CI Ⓒ.. OH₂ O CH₂ CH₂ CH3 resonance CH₂ - H₂O loss of a leaving group resonance secondary carbocation CH₂ CH3 - H₂O methyl migration (rearrangement) CH₂ loss of a leaving group - &
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