William E. Acree, Jr. 2 2.902e+02 Ambient temperature 4 2.902 $\pu{K}$ -1 2.113e-01 Mole fraction - Liquid (1) 4 2.113 1 -1 7.887e-01 Mole fraction - Liquid (2) 4 7.887 1 1 2 2.920e+02 Ambient temperature 4 2.920 $\pu{K}$ -1 2.217e-01 Mole fraction - Liquid (1) 4 2.217 1 -1 7.783e-01 Mole fraction - Liquid (2) 4 7.783 1 2 2 2.960e+02 Ambient temperature 4 2.960 $\pu{K}$ -1 2.512e-01 Mole fraction - Liquid (1) 4 2.512 1 -1 7.488e-01 Mole fraction - Liquid (2) 4 7.488 1 3 2 2.982e+02 Ambient temperature 4 2.982 $\pu{K}$ -1 2.570e-01 Mole fraction - Liquid (1) 4 2.570 1 -1 7.430e-01 Mole fraction - Liquid (2) 4 7.430 1 4 2 3.016e+02 Ambient temperature 4 3.016 $\pu{K}$ -1 2.801e-01 Mole fraction - Liquid (1) 4 2.801 1 -1 7.199e-01 Mole fraction - Liquid (2) 4 7.199 1 5 2 3.028e+02 Ambient temperature 4 3.028 $\pu{K}$ -1 2.892e-01 Mole fraction - Liquid (1) 4 2.892 1 -1 7.108e-01 Mole fraction - Liquid (2) 4 7.108 1 6 2 3.083e+02 Ambient temperature 4 3.083 $\pu{K}$ -1 3.204e-01 Mole fraction - Liquid (1) 4 3.204 1 -1 6.796e-01 Mole fraction - Liquid (2) 4 6.796 1 7 1 Solubility, Solubility data series Constant temperature bath and a precision thermometer.<br>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 visual noting the same temperature at which the last trace of solid solute disappeared. The International Union of Pure and Applied Chemistry Srivastava, R. D.; Gupta, P. D.; J. Indian Chem. Soc. 1967, 44, 960-963. paper 85-01-8 1 C14H10 InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H YNPNZTXNASCQKK-UHFFFAOYSA-N 178.229 Phenanthrene Purity not given, British Drug Houses, United Kingdom, was recrystallized and sublimed. 98-95-3 2 C6H5NO2 InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H LQNUZADURLCDLV-UHFFFAOYSA-N 123.109 Nitrobenzene Purity not given, British Drug Houses, was dried over and distilled. Phenanthrene with Nitrobenzene