Enantiopure diphenylprolinols were synthesized from a commercially available starting material. The utility of ¹H NMR spectroscopy for the differentiation of enantiomers using these chiral compounds as CSAs is stated, and their capacity acting as receptors for various carboxylic acids via hydrogen bonding is exploited. A linear relationship has been observed between the experimental and observed values of ee indicating the possible use of these compounds for quick and reliable analysis of enantiomerically enriched samples of various mandelic acids. From the experiments performed a preliminary conclusion indicated that the diphenylprolinol 1b with the free NH and OH is most effective in the chiral discrimination of carboxylic acids in ¹H NMR.