The complete set of deuterium-induced intrinsic ' ' C NMR isotope shifts, "A("C), for norbornane have been determined from the isotopomeric monodeuteriated systems, and the results are discussed with respect to structure. No correlation is found between 'A values and the s character of the CD bond hybrid. For vicinal isotope effects, however, a quantitative correlation with the dihedral angles of the intervening "C-C-C-D bond fragment can be formulated: