Experimental ionization energies I4s and I3d are listed for K[Ar]4s1, K[Ar]3d1, and Ca to Cu in the lowest states of M[Ar]4s23dn and M[Ar]4s13dn+1. In a plot comparing
-I4s(4s23dn) with -I3d(4s13dn+1), the lower one selects the ground state. Features of that plot are explained with a plot of the corresponding Hartree-Fock (HF) minus valence-exchange energies. A new definition is given for the effective charge Zf. HF orbital energies. A new definition is given for the effective charge Zf. HF orbital energies e4s and e3d are used in concert with I4s and I3d to answer four questions: Why does the 4s sublevel fill before 3d? Why is ionization easier for 4s than 3d? When 4s23dn has e3d < e4s, why doesn't 4s23dn -> 4s13dn+1? Why are Cr and Cu each 4s13dn+1 instead of 4s23dn?
More Information
Citation
Bills, James L. J. Chem. Educ.1998 75 589.
Keywords
Introductory/High School Chemistry, Inorganic Chemistry, Physical/Theoretical
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