The synthesis of acid orange 7 is shown below. Please answer the following questions. 8 7. 1 2 OH NH3 N2 3 5 4 SO3 Na 1) NażCO3 2) NaNO2, HCI A ß-naphthol LOH 1 Step 1 2 Step 2 Acid orange 7 In step 2, please choose all that explain the selectivity of this electrophilic aromatic substation reaction Select one or more: O A. Because hydroxyl group (-OH) is a ortho/para director, compound 2 selectively adds to the 1 position of B-naphthol. O B. Because hydroxyl group (-OH) is a meta director, compound 2 selectively adds to the 1 position of B-naphthol O C. Because hydroxyl group (-OH) is electron donation group, compound 2 selectively adds to the right ring of B-naphthol O D. Because hydroxyl group (-OH) is electron withdrawing group, compound 2 selectively adds to the right ring of B-naphthol

The synthesis of acid orange 7 is shown below. Please answer the following questions. 8 7. 1 2 OH NH3 N2 3 5 4 SO3 Na 1) NażCO3 2) NaNO2, HCI A ß-naphthol LOH 1 Step 1 2 Step 2 Acid orange 7 In step 2, please choose all that explain the selectivity of this electrophilic aromatic substation reaction Select one or more: O A. Because hydroxyl group (-OH) is a ortho/para director, compound 2 selectively adds to the 1 position of B-naphthol. O B. Because hydroxyl group (-OH) is a meta director, compound 2 selectively adds to the 1 position of B-naphthol O C. Because hydroxyl group (-OH) is electron donation group, compound 2 selectively adds to the right ring of B-naphthol O D. Because hydroxyl group (-OH) is electron withdrawing group, compound 2 selectively adds to the right ring of B-naphthol

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.67P

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