The multiresonant coherent multidimensional spectroscopy study of D(2)O in AOT micelles reveals two unexpected features in addition to those expected for D(2)O. These features appear when the excitation pulse time ordering defines either fully coherent Liouville pathways or partially coherent pathways where there are intermediate populations. The features shift as the excitation pulse ordering changes between the two sets of pathways. They are attributed to the asymmetric stretch mode of CO(2) that is formed by the infrared excited decarboxylation of AOT. The cross-peaks' intensity is enhanced when the excitation pulse is resonant with the CO(2) P and R branches for the fully coherent pathways, but they are depressed at the P and R branch resonances for the partially coherent pathways. The enhancement is attributed to the simultaneous production of CO(2) during the first excitation pulse when it is resonant with both the CO(2) and the D(2)O. The depression is attributed to the absorption of the last excitation pulse by the CO(2) produced by the previous two excitation pulses. We believe that the decarboxylation occurs because of energy transfer from multiply excited D(2)O molecules. It may cause a Norrish type I alpha-cleavage in the AOT that is followed by a Hunsdiecker reaction beta-scission of the radical to form the CO(2). This experiment demonstrates the marriage of infrared induced chemistry and multiresonant coherent multidimensional spectroscopy into a single nonlinear process.