Excess molar enthalpies (H-E) at 298.15 K of N,N-dimethylformamide with a s
eries of ketones: methyl ethyl ketone (MEK), methyl propyl ketone (MIPK), d
iethyl ketone (DEK), methyl isobutyl ketone (MIBK), cyclopentanone (CP) and
cyclohexanone (CH) have been measured by using a Parr 1451 solution calori
meter, as a function of mole fraction of the N,N-dimethylformamide. The exp
erimental H-E values are positive for ail binary mixtures over the entire r
ange of composition. The excess enthalpies of the above mentioned binary sy
stems, were used to discuss interactions between the ketonic (>CO) and DMF
molecules. The results are interpreted to gain insight into the changes in
molecular association equilibria and structural effects in these systems. W
hen the compounds are mixed, the changes that occur in association equilibr
ia are evidently rupture of the hydrogen bonds in pure compounds and the fo
rmation of OH... CO hydrogen bonds between the compounds. (C) 1999 Elsevier
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