1. A methoxy group (-OMe) on an aromatic ring is electron-withdrawing when considering inductive effects, yet the methoxy group is categorized as an electron-donating group. Why? 2. Kinetic enolates form faster than thermodynamic enolates, but they do not predominate at equilibrium. Why not? 3. Tertiary carbocations and radicals are more stable than primary carbocations and radicals. Why?
1. A methoxy group (-OMe) on an aromatic ring is electron-withdrawing when considering inductive effects, yet the methoxy group is categorized as an electron-donating group. Why? 2. Kinetic enolates form faster than thermodynamic enolates, but they do not predominate at equilibrium. Why not? 3. Tertiary carbocations and radicals are more stable than primary carbocations and radicals. Why?
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 17E
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1. A methoxy group (-OMe) on an
2. Kinetic enolates form faster than
3. Tertiary carbocations and radicals are more stable than primary carbocations and radicals. Why?
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