Hi there,
I was investigating tetrahydrofuran as a solvent that I was planning on mixing with an acid. According to Reichardt (2005) p. 107, tetrahydrofuran undergoes tautomerism to an enol. Would this cause tetrahydrofuran to break down say in the presence of an acid? I was just wondering because I would need the tetrahydrofuran to remain intact as a solvent.
Reference
Reichardt, C. Solvents and solvent effects in organic chemistry, 3rd ed. 2005. Wiley.