“…In this study, the degradation of boscalid is likely due to attack of hydroxyl radicals at −H in the three rings (benzene and pyridine rings) leading to four mono and di hydroxylated products and other carboxylic acids (Lagunas-Allué, Martínez-Soria, Sanz-Asensio, Salvador, Ferronato, & Chovelon, 2010). Furthermore, the suggested degradation of imidacloprid is due to the reaction of hydroxyl radicals to form 6-chloronicotinic aldehyde and 6-chloronicotinic acid (Agüera, Almansa, Malato, Maldonado, & Fernández-Alba, 1998;Malato, et al, 2001). …”