The 60 MHz1H NMR spectra of racemic vinclozolin,1, have been studied at 28° in CDC13solution with the chiral reagent tris[3-(heptafluoropropylhydroxymethylene)-d-camphorato]europium(III),2, by incremental additions of (6,6,7,7,8,8,8-heptafluoro-2,2-di-methyl-3,5-octanedionato)silver(I),3.Although the solution of1with2displayed substantial downfield lanthanide-induced shifts, Δδ, and enantiomeric shift differences, ΔΔδ, for selected nuclei, relative to the spectrum of unshifted1, additions of3to the solution of1and2were unexpectedly found to dramatically reduce the magnitudes of both Δδ and ΔΔδ.