Question: 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

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

Pentafluorophenol is readily prepared by heating hexafluorobenzene with potassium hydroxide

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

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

Step by Step Solution

3.40 Rating (162 Votes )

There are 3 Steps involved in it

1 Expert Approved Answer
Step: 1 Unlock

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

blur-text-image
Question Has Been Solved by an Expert!

Get step-by-step solutions from verified subject matter experts

Step: 2 Unlock
Step: 3 Unlock

Document Format (1 attachment)

Word file Icon

924-C-OC-A (1200).docx

120 KBs Word File

Students Have Also Explored These Related Organic Chemistry Questions!