The dipolar elements (Bx, By, Bz) of the α-hydrogen hyperfine coupling tensor (αA) are used to calculate unpaired spin density (ρ) and bond lengths (RH) by using the two center dipole equations derived by Gordy (Ref. 1). Bz is used as a measure of ρ in the equation Bz=Qdipz ρ with Qdipz =38.7 MHz. The αH-C bond length of electron gain π radicals and alkyl radicals are found to be 0.05–0.10 Å shorter than in comparable nonradicals while in electron loss π radicals the bond lengths are longer by 0.04–0.09 Å. The two center dipole formalism appears to be useful as an analytical method for distinguishing electron loss π radicals from electron gain π radicals. It is suggested that the isotropic component of αH hfc is affected by spin density β to the αH of interest, accounting for a significant portion of the variability in QHCH in the McConnel (Ref. 2) equation, αA =QHCHρ.