он 1. aqueous H2SO4 -CH3 CH3 2. H2SO4 H20 но 130° a = Proton transfer d = El Elimination f= Sy1 Nucleophilic substitution b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2.
он 1. aqueous H2SO4 -CH3 CH3 2. H2SO4 H20 но 130° a = Proton transfer d = El Elimination f= Sy1 Nucleophilic substitution b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2.
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...
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