William E. Acree, Jr. 2 3.090e+02 Ambient temperature 4 3.090 $\pu{K}$ -2 1.03e-02 Mole fraction - Liquid (1) 3 1.03 1 -1 9.897e-01 Mole fraction - Liquid (2) 4 9.897 1 1 2 3.156e+02 Ambient temperature 4 3.156 $\pu{K}$ -2 1.30e-02 Mole fraction - Liquid (1) 3 1.30 1 -1 9.870e-01 Mole fraction - Liquid (2) 4 9.870 1 2 2 3.238e+02 Ambient temperature 4 3.238 $\pu{K}$ -2 1.73e-02 Mole fraction - Liquid (1) 3 1.73 1 -1 9.827e-01 Mole fraction - Liquid (2) 4 9.827 1 3 2 3.328e+02 Ambient temperature 4 3.328 $\pu{K}$ -2 2.25e-02 Mole fraction - Liquid (1) 3 2.25 1 -1 9.775e-01 Mole fraction - Liquid (2) 4 9.775 1 4 2 3.434e+02 Ambient temperature 4 3.434 $\pu{K}$ -2 3.15e-02 Mole fraction - Liquid (1) 3 3.15 1 -1 9.685e-01 Mole fraction - Liquid (2) 4 9.685 1 5 1 Solubility, Solubility data series Constant temperature bath and a precision thermometer. Mixtures of known concentrations sealed in glass ampoules and placed in constant temperature to equilibrate. Samples were rotated while bath temperature slowly increased. Solubility determined by noting the temperature at which the last trace of solid solute disappeared. The International Union of Pure and Applied Chemistry McLaughlin, E.; Zainal, H. A.; J. Chem. Soc. 1959, 863-867. paper https://doi.org/10.1039/jr9590000863 71-43-2 2 C6H6 InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H UHOVQNZJYSORNB-UHFFFAOYSA-N 78.1118 Benzene “AnalaR”, was dried over sodium wire and freshly distilled before use. 120-12-7 1 C14H10 InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H MWPLVEDNUUSJAV-UHFFFAOYSA-N 178.229 Anthracene Purity, source and purification procedure not specified. Anthracene with Benzene