The Gauche effect characterizes any gauche rotamer which is actually more stable than the anti rotamer.This effect is present in 1,2-difluoroethane (H2FCCFH2) for which the gauche conformation is more stable by 2.4 to 3.4 kJ/mole in the gas phase. Another example is 1,2-dimethoxyethane. In stereochemistry, gauche interactions hinder bond rotation.