Ammonia/hydrogen blends have received some attention toward the development of new technologies focused on gas turbine combustion systems, as doping of hydrogen in ammonia enhances flame speed and stability while decreasing ignition energy. One of the challenges of these blends relies on the appropriate computational modeling of their combustion properties in combination with the complex hydrodynamics inherent to flow control techniques such as swirling flows, which are known to be the main method of flame stabilization in current gas turbines. Moreover, it is well-known that large reaction kinetic models are difficult to employ in these computational analyses, thus increasing the difficulty of obtaining reliable methods for the design of new combustors. Therefore, this research analyses a reduced chemical reaction mechanism, namely Okafor’s mechanism, comparing its performance and accuracy against obtained experiments. Emission measurements and non-intrusive laser techniques (LDA) were employed to validate models running on CHEMKIN-PRO flow reactors and RANS Complex Chemistry. Once validated, the study identified the main contributors and reaction kinetics of NH₂ and NO consumption, hence evaluating the process via production rates and sensitivity analysis of various important reactions. The results depicted positive correlation between NH₂ formation and heat release, N₂, H₂O, N₂O, NH, NNH, NO, O formation, whereas NH₃, N₂H₃ and NO₂ have shown negative correlation. Statistical correlations supported these findings but unfortunately were inconclusive to the impacts of vorticity and turbulence over the production/consumption of amidogen. Sensitivity analysis has shown NH₂ radicals and atomic N to be the main contributors of NO formation in the flame zone, although most of the NO formed in the flame zone shown to be consumed at the post-flame zone due to the presence of NH_x radicals and atomic N.