The synthesis of an azo dye is shown below. Please answer the following questions. NH2 N2 1) Na2CO3 2) NANO2, HCI B N-N A Step 1 Step 2 2 1 3 2. In step 2, Why compound 2 selectively adds to the para position of aniline? (multiple answers) Oa) amino group is an electron-withdrawing group ob) amino group is an electron-donating group Oc) amino group is an ortho-para directing group Od) para positions is more sterically hindered

Macroscale and Microscale Organic Experiments
7th Edition
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Kenneth L. Williamson, Katherine M. Masters
Chapter7: Extraction
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The synthesis of an azo dye is shown below. Please answer the following questions.
NH2
*N2
1) Na2CO3
2) NANO2, HCI
B N-N A
ŠOH
Step 1
Step 2
1
2. In step 2, Why compound 2 selectively adds to the para position of aniline? (multiple answers)
Oa) amino group is an electron-withdrawing group
ob) amino group is an electron-donating group
Oc) amino group is an ortho-para directing group
Od) para positions is more sterically hindered
Transcribed Image Text:The synthesis of an azo dye is shown below. Please answer the following questions. NH2 *N2 1) Na2CO3 2) NANO2, HCI B N-N A ŠOH Step 1 Step 2 1 2. In step 2, Why compound 2 selectively adds to the para position of aniline? (multiple answers) Oa) amino group is an electron-withdrawing group ob) amino group is an electron-donating group Oc) amino group is an ortho-para directing group Od) para positions is more sterically hindered
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