38090
Is the intramolecular hydrogen bonding responsible for the conformational preference of trans-2-fluorocyclohexanol?
The occurrence of intramolecular hydrogen bond involving fluorine and hydroxyl group (F---H-O) for the trans-2-fluorocyclohexanol has been investigated through NMR and Infrared spectroscopy supported by theoretical calculations. The compound under investigation was synthesized and purified, after that its 1H, 13C and 19F NMR spectra were obtained in solvent of different polarities.