The reaction of 2-methoxy-1 nitronaphthalene with various Grignard reagents has been examined. Alkylmagnesium halides such as CH3MgBr, PhCH2MgBr, PhCH2CH2MgBr, C2H5MgBr, and i-C3H7MgBr give 1,6-addition products almost exclusively, while PhMgBr gives instead comparable amounts of 1,4- addition and reductive 1,2-addition products. Hex-5-enylmagnesium bromide reacts giving two 1,6- addition products, one containing a straight chain and the other one a cyclized alkyl fragment, where the ratio of the two decreases with decreasing temperature. The reactivity order (i-C3H7 > PhCH2≃ C2H5 > PhCH2CH2 > CH3) established by competitive reactions along with the reactivrty pattern shown by hex-5-enylmagnesium bromide was taken as clear evidence for a single-electron transfer (s.e.t.) process. A mechanism involving s.e.t. from Grignard reagent to nitroarene followed by collapse within the solvent cage of the two radicals thus formed (geminate combination) or, to a lesser extent, out of the cage (non-geminate combination), is suggested. The reaction of 1-nitronaphthalene with methyl-, isopropyl- and hex-5-enyl-magnesium bromides indicates that the distribution of isomeric 2- and 4- alkylated products is determined by the reactivity of the ring positions for both geminate and non-geminate combination. No firm mechanistic conclusions were reached regarding the reaction of PhMgBr.