Is a metal chelate symmetric, with the motion of the metal described by a single-well potential, or is it asymmetric, in a double-well potential? For hydrogen, this is the familiar question of the symmetry of a hydrogen bond. The molecular symmetry of MLn complexes (M = Li, Na, K, Al, Pd, Rh, Si Sn, Ge, Sb, etc.; L is the anion of 3-hydroxy-2-phenylpropenal) in solution is now probed with the method of isotopic perturbation of equilibrium. A statistical mixture of 3-hydroxy-2-phenylpropenal-d(0), -1-d, and -1,3-d(2) was synthesized and converted to various metal complexes. Some complexes show two aldehydic signals, which means that their ligands are monodentate. For LiL, NaL, and KL, the C-13 NMR isotope shifts, delta(CH(D)) - delta(CH(H)), for the aldehydic Ch groups are small and negative, consistent with L- being a resonance hybrid. They are small and positive for AIL(3), PdL2, Rh(CO)(2)L, SiX3L, SiL3+X-, (CF3)(3)GeL, SbCl4L, (EtO)(4)TaL, and (EtO)(4)NbL. The positive isotope shifts are unusual, but since they are small and temperature independent, they are intrinsic and indicate that these metal chelates are symmetric, as expected. Large positive isotope shifts, up to 400 ppb, are observed for Ph3GeL, Me3GeL, Ph2GeL2, Bu3SnL, and Ph4SbL. However, it is likely that these are monodentate complexes undergoing rapid metal migration, as judged from the X-ray crystal structures of Ph3SnL and Ph(4)ShL. NMR experiments indicate an intermolecular mechanism for exchange, which may be a bimolecular double metal transfer. It is remarkable that the isotope shifts in these five complexes demonstrate that they are asymmetric structures, even though they appear from other NMR evidence to be symmetric chelates.