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The first title benzoyl amide, C17H20CINO5 (3a), crystallizes in the monoclinic space group P21/c with Z = 4 and the second, C19H24CINO5 (3b), also crystallizes in P21/c with Z = 8 (Z' = 2), thus there are two independent molecules in the asymmetric unit. In 3a, the phenyl ring makes a dihedral angle of 50.8 (3)° with the amide moiety with the C O group on the same side of the molecule as the C--Cl group. One methoxy group is almost in the plane of the benzene ring, while the ethoxy and other methoxy substituent are arranged on opposite sides of the ring with the ethoxy group occupying the same side of the ring as the C=O group in the amide moiety. For one of the two molecules in 3b, both the amide and 5,5-dimethyl-3-oxocyclohex-1-en-1-yl moieties are disordered over two sets of sites with occupancies of 0.551 (2)/0.449 (2) with the major difference between the two conformers being due to the conformation adopted by the cyclohex-2-en-1-one ring. The three molecules in 3b (i.e., the undisordered molecule and the two disorder components) differ in the arrangement of the subsituents on the phenyl ring and the conformation adopted by their 5,5-dimethyl-3-oxocyclohex-1-en-1-yl moieties. In the crystal of 3a, N--H…O hydrogen bonds link the molecules into a zigzag chain propagating in the [001] direction. For 3b a combination of C--H…O and N--H…O intermolecular interactions link the molecules into a zigzag ribbon propagating in the [001] direction. [ABSTRACT FROM AUTHOR]