A product of the following reaction would be Benzene 1/2 l2 + HNO3 O 1,3-Diiodobenzene O lodobenzene O 1,2-Diiodobenzene O 1,1-Dichloro-iodobenzene O 1,4-Diiodobenzene
A product of the following reaction would be Benzene 1/2 l2 + HNO3 O 1,3-Diiodobenzene O lodobenzene O 1,2-Diiodobenzene O 1,1-Dichloro-iodobenzene O 1,4-Diiodobenzene
Chemistry
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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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![A product of the following reaction would be
Benzene
1/2 12 + HNO3
O 1,3-Diiodobenzene
O. lodobenzene
O 1,2-Diiodobenzene
O 1,1-Dichloro-iodobenzene
O 1,4-Diiodobenzene](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F450044ef-db4b-4b73-a24e-98f3627ca204%2Fa7d5d85e-d39b-4cfb-98a7-c720deac69b4%2F2die0r2_processed.jpeg&w=3840&q=75)
Transcribed Image Text:A product of the following reaction would be
Benzene
1/2 12 + HNO3
O 1,3-Diiodobenzene
O. lodobenzene
O 1,2-Diiodobenzene
O 1,1-Dichloro-iodobenzene
O 1,4-Diiodobenzene
Expert Solution
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Step 1
Halogenation of benzene takes place by an electrophilic aromatic substitution reaction mechanism. Chlorination and bromination of benzene take place in the presence of Lewis acid catalyst. The iodination of benzene cannot proceed in the presence of Lewis acid catalyst because the bond energy change in the iodination reaction is unfavorable.
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