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Irradiation of N-aryl O-aryl carbamates has been carried out in H2O/CH3CN (1 : 1 v/v) solutions at λ>290 nm. When chlorine is on the N-aryl ring, halogen-substituted products are found. These photoproducts derive from the trapping of the intermediate radical cation by water and, even, by acetonitrile leading to phenols and N-arylacetamides (photo-Ritter products), respectively.  Unsubstituted N-aryl carbamates slowly  undergo photo-Fries reaction

Photochemical Behaviour of Carbamates Structurally Related to Herbicides in Aqueous Media: Nucleophilic Solvent Trapping versus Radical Reactions