Copy the figure shown below onto your scratch paper. Na SCH, Box 1 NaO Box 2 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 (t,0.) Br formal charge (0,) Ca formal charge (0 Phrase (A.G) Box 1: Вох 2: 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
Transcribed Image Text: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
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