“…The p-type electron orbital of N is bound to the benzene ring, making the ethyl group at the N-position easily attacked due to electron delocalization. Therefore, hydroxyl radicals produced in the electrocatalytic oxidation first cause the N-de-ethylation of RhB to form product I (C 26 H 27 N 2 O 3 + , m / z = 415), product II (C 24 H 23 N 2 O 3 + , m / z = 387), product III (C 20 H 15 N 2 O 3 + , m / z = 331). , Subsequently, hydroxyl radicals attack the N-de-ethylation products to induce denitrification and decarboxylation reactions, thus forming product IV (C 20 H 15 NO 3 , m / z = 318) and product V (C 19 H 15 NO, m / z = 274) . Then, hydroxyl radicals continue to attack the structural center of RhB, leading to the destruction of the conjugated xanthene structure, e.g., the cleavage and ring-opening of product V form product VI (C 13 H 9 O, m / z = 181) and small molecule organic acids, such as product VII (C 7 H 6 O 4 , m / z = 154) and product VIII (C 7 H 6 O 2 , m / z = 122) …”