Kinetic studies of the reactions of some phenols and alkyl aryl ethers with dinitrogen pentoxide in perfluorocarbon solvents

The reaction of dinitrogen pentoxide in perfluorocarbon solvents with pheno ls and alkyl aryl ethers carrying halogeno ring-substituents results in nit rodehydrogenation. Rate measurements show that the preferred orientation of nitration is ortho > para > meta to the hydroxy group; the kinetic isotope effect, k(H)/k(D), has a value close to unity. Phenols show considerably h igher reactivity than similarly substituted alkyl phenyl ethers; and a mech anism is suggested involving initial interaction of N2O5 with the hydroxy f unction followed by reaction via cyclic transition states.