When determining the reducing character of hydrides in the nitrogen family (Group 15), we prioritize bond enthalpy over basic strength because bond enthalpy is a more accurate representation of the energy required to break the bond between the element and hydrogen. The bond enthalpy reflects the strength of the bond and the energy required to remove the hydrogen atom.
In the context of reducing character, a stronger reducing agent is one that more readily donates electrons or removes hydrogen atoms. A hydride with a lower bond enthalpy requires less energy to break the bond and release hydrogen, making it a stronger reducing agent.
While basic strength can indicate the availability of electrons, it does not directly correlate with the reducing character of hydrides. Basic strength is more relevant when considering proton acceptability in acid-base reactions.
Therefore, in the case of Group 15 hydrides (such as NH3, PH3, AsH3, and SbH3), bond enthalpy is considered the more appropriate factor to analyze reducing character, as it gives a clearer picture of the energy required for the hydride to act as a reducing agent.