Why does naphthalene undergo electrophilic substitution at C1 instead of C2? Could you draw a structure for the intermediate that helps explain this?
Why does naphthalene undergo electrophilic substitution at C1 instead of C2? Could you draw a structure for the intermediate that helps explain this?
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 19.70P: In Problem 7.28, we saw this two-step sequence in Johnsons synthesis of the steroid hormone...
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Why does naphthalene undergo electrophilic substitution at C1 instead of C2? Could you draw a structure for the intermediate that helps explain this?
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