Why we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the ortho positions which is where the bromine is added. b. Because the amine group is a strong ortho, para director which is what controls the regiochemical outcome of this bromination. c. Step 4 is unessesary. The symmetry of compound 3 allows for the bromination to be regioselective and give compound 5. 5. There will be a mixture of products because there is no selectivity for a major product.

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Why we need step 3 before step 4?

a. Because the nitro group increases the electrophilicity at the ortho positions which is where the bromine is added.
b. Because the amine group is a strong ortho, para director which is what controls the regiochemical outcome of this bromination.
c. Step 4 is unessesary. The symmetry of compound 3 allows for the bromination to be regioselective and give compound 5.
5. There will be a mixture of products because there is no selectivity for a major product.
Step 3
Step 4
Br
NO2
NH2
NH2
3
4
5
Transcribed Image Text:Step 3 Step 4 Br NO2 NH2 NH2 3 4 5
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