Box 1 Box 2 Box 3 HBr Then, complete the figure on your scratch paper by drawing out the intermediates and arrow-pushing mechanism in Boxes 1-3 that explain the formation of the final products shown. You should start your arrow-pushing in Box 1, and you will use all boxes. Now, report the formal charges (+,0,-) that appear on C Cy, and bromine atoms in each box, and match the contents of each box to a single phrase (A-H) that best describes the mechanistic step that occurs in each box. A. A hydride shift occurs. B. A methyl shift occurs C. A nucleophile attacks a tertiary carbocation D. A leaving group leaves. E. A nucleophile attacks a secondary carbocation. F. Br is protonated, Cy is deprotonated, and a pi bond forms G. A carbocation attacks the Br H. Br is protonated, Cy is deprotonated, and a pi bond forms Cr formal charge (+0) Cy fomal charge (+0a Br formal charge (+0.) Phrase (A-H) Вох 1: 0 Box 2: Вох 3: Products: 0

Box 1 Box 2 Box 3 HBr Then, complete the figure on your scratch paper by drawing out the intermediates and arrow-pushing mechanism in Boxes 1-3 that explain the formation of the final products shown. You should start your arrow-pushing in Box 1, and you will use all boxes. Now, report the formal charges (+,0,-) that appear on C Cy, and bromine atoms in each box, and match the contents of each box to a single phrase (A-H) that best describes the mechanistic step that occurs in each box. A. A hydride shift occurs. B. A methyl shift occurs C. A nucleophile attacks a tertiary carbocation D. A leaving group leaves. E. A nucleophile attacks a secondary carbocation. F. Br is protonated, Cy is deprotonated, and a pi bond forms G. A carbocation attacks the Br H. Br is protonated, Cy is deprotonated, and a pi bond forms Cr formal charge (+0) Cy fomal charge (+0a Br formal charge (+0.) Phrase (A-H) Вох 1: 0 Box 2: Вох 3: Products: 0

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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Copy the figure shown below onto your scratch paper. Вох 1 Na Box 2 Na O SCH3 Br Br SCH3 Then, complete the figure on your șcratch paper by drawing out the intermediates and arrow-pushing mechanism in Boxes 1-2 that explain the formation of the final products shown. You should start your arrow-pushing in Box 1, and you will use all boxes. Now, report the formal charges (+,0,-) that appear on the sulfur, bromine, and alpha carbon atoms in each box, and match the contents of each box to a single phrase (A-G) that best describes the mechanistic step that occurs in each box. A. A nucleophile attacks a tertiary carbocation. B. A nucleophile attacks a secondary carbocation. C. A nucleophile attacks, and a leaving group leaves. D. Br is protonated, and S is deprotonated. E. A leaving group leaves. F. S is protonated, and Br is deprotonated. G. A carbocation attacks S. S formal charge (±,0,-) Br formal charge (+,0,-) Caformal charge (+,0,-) Phrase (A-G) Вох 1: - Вох 2: Products: 0
4. Draw the mechanism that accounts for the formation of the product under the conditions shown. You may not add any other reagents. Be sure to show: all intermediate structures that occur in the course of the mechanism, any important resonance structures that play a role in the process, what if anything is added or lost in each step, and all formal charges on the structures. CHO H+ HO-C-H HO OH H-C-OH CH,OH НО 1 2 = 3
Copy the figure shown below onto your scratch paper. Вох 1 Na Вох 2 Na® SCH3 Br Br SCH3 Then, complete the figure on your scratch paper by drawing out the intermediates and arrow-pushing mechanism in Boxes 1-2 that explain the formation of the final products shown. You should start your arrow-pushing in Box 1, and you will use all boxes. Now, report the formal charges (+,0,-) that appear on the sulfur, bromine, and alpha carbon atoms in each box, and match the contents of each box to a single phrase (A-G) that best describes the mechanistic step that occurs in each box. A. A nucleophile attacks a tertiary carbocation. B. A nucleophile attacks a secondary carbocation. C. A nucleophile attacks, and a leaving group leaves. D. Br is protonated, and S is deprotonated. E. A leaving group leaves. F.S is protonated, and Br is deprotonated. G. A carbocation attacks S. S formal charge (+,0,-) Br formal charge (+,0,-) Ca formal charge (+,0,-) Phrase (A-G) Воx 1: — 0. Box 2: Products: 0
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QUESTION 7 Copy the figure shown below onto your scratch paper. Box 1 Box 2 Box 3 HBr Br Then, complete the figure on your scratch paper by drawing out the intermediates and arrow-pushing mechanism in Boxes 1-3 that explain the formation of the final products shown. You should start your arrow-pushing in Box 1, and you will use all boxes. Now, report the formal charges (+,0,-) that appear on the alpha carbon, beta carbon, and bromine atoms in each box, and match the contents of each box to a single phrase (A-H) that best describes the mechanistic step that Occurs in each box. A. A hydride shift occurs. B. A methyl shift occurs. C. A nucleophile attacks a tertiary carbocation. D. A leaving group leaves. E. A nucleophile attacks a secondary carbocation. F. Br is protonated, the alpha carbon is deprotonated, and a pi bond forms G. A carbocation attacks the Br. H. Br is protonated, the beta carbon is deprotonated, and a pi bond forms Ca formal charge (+,0,-) CR formal charge (+,0,-) Br…
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