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The following acid-base reaction is reversible enough to neither be considered significantly product or reactant favored. In terms of ARIO, which best explains how it is that the C-H proton of the ketone is just as acidic as O-H proton of tert-butanol? & pka = 16.7 j H pka = 16.5 Atom Resonance Induction Orbital

The following acid-base reaction is reversible enough to neither be considered significantly product or reactant favored. In terms of ARIO, which best explains how it is that the C-H proton of the ketone is just as acidic as O-H proton of tert-butanol? & pka = 16.7 j H pka = 16.5 Atom Resonance Induction Orbital

Organic Chemistry
Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 64AP: The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold...
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The following acid-base reaction is reversible enough to neither be considered significantly product or reactant favored. In terms of ARIO, which best explains how it is that the C-H proton of the ketone is just as acidic as O-H proton of tert-butanol? & pka = 16.7 j H pka = 16.5 Atom Resonance Induction Orbital
Transcribed Image Text:The following acid-base reaction is reversible enough to neither be considered significantly product or reactant favored. In terms of ARIO, which best explains how it is that the C-H proton of the ketone is just as acidic as O-H proton of tert-butanol? & pka = 16.7 j H pka = 16.5 Atom Resonance Induction Orbital
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