Pentafluorophenol is readily prepared by heating hexafluorobenzene with potassium hydroxide in tert-butyl alcohol: What is the most

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Pentafluorophenol is readily prepared by heating hexafluorobenzene with potassium hydroxide in tert-butyl alcohol:

What is the most reasonable mechanism for this reaction? Comment on the comparative ease with which this conversion occurs.

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Organic Chemistry

ISBN: 978-0072905014

4th edition

Authors: Francis A. Carey

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Question Posted: Apr 30, 2016 01:54 PM

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Pentafluorophenol is readily prepared by heating hexafluorobenzene with potassium hydroxide in tert-butyl alcohol: What is the most

Question:

I. KOH, (CH) COH reflux, I h OH Hexafluorobenze ne Pentafluorophenol (71%)

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Nucleophilic aromatic substitution by the eliminat...View the full answer

Organic Chemistry

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