Role of functional-group position in determining the interaction between structure-making and structure-breaking solutes. A microcalorimetric study of the interactions in aqueous solutions between positional isomers of alkan-m-ols and urea or biuret

Enthalpies of dilution of ternary aqueous solutions containing biuret or urea and positional isomers of alkan-m-ols have been determined by flow microcalorimetry at 298.15 K. Pairwise cross-interaction coefficients of the virial expansion of the excess enthalpies were evaluated. The values of the coefficients are positive, depending in a very complex manner on the length of the alkyl chain and on the position occupied by the hydroxy group along the alkyl chain. The behaviour of these systems seems to be determined by a balance between favourable hydrophilic-hydrophilic and repulsive hydrophilic-hydrophobic interactions. When the hydroxy group occupies more central positions, unfavourable interactions prevail and the cross coefficient for the alkanol bearing the longest alkyl chain is almost zero.