Glenn T. Hefter -1 4e-01 Ambient temperature 1 4 °C 1 -4 4.01e-04 Mole fraction - Liquid (1) 3 4.01 1 -1 1.74e-01 Relative mass - solution (1) 3 1.74 g₁/100 g sln 0 5.2e+00 Ambient temperature 2 5.2 °C 2 -4 4.17e-04 Mole fraction - Liquid (1) 3 4.17 1 -1 1.81e-01 Relative mass - solution (1) 3 1.81 g₁/100 g sln 1 1.00e+01 Ambient temperature 3 1.00 °C 3 -4 4.15e-04 Mole fraction - Liquid (1) 3 4.15 1 -1 1.80e-01 Relative mass - solution (1) 3 1.80 g₁/100 g sln 1 1.49e+01 Ambient temperature 3 1.49 °C 4 -4 4.10e-04 Mole fraction - Liquid (1) 3 4.10 1 -1 1.78e-01 Relative mass - solution (1) 3 1.78 g₁/100 g sln 1 2.10e+01 Ambient temperature 3 2.10 °C 5 -4 4.13e-04 Mole fraction - Liquid (1) 3 4.13 1 -1 1.79e-01 Relative mass - solution (1) 3 1.79 g₁/100 g sln 1 2.50e+01 Ambient temperature 3 2.50 °C 6 -4 4.13e-04 Mole fraction - Liquid (1) 3 4.13 1 -1 1.79e-01 Relative mass - solution (1) 3 1.79 g₁/100 g sln 1 2.56e+01 Ambient temperature 3 2.56 °C 7 -4 4.13e-04 Mole fraction - Liquid (1) 3 4.13 1 -1 1.79e-01 Relative mass - solution (1) 3 1.79 g₁/100 g sln 1 3.02e+01 Ambient temperature 3 3.02 °C 8 -4 4.24e-04 Mole fraction - Liquid (1) 3 4.24 1 -1 1.84e-01 Relative mass - solution (1) 3 1.84 g₁/100 g sln 1 3.49e+01 Ambient temperature 3 3.49 °C 9 -4 4.36e-04 Mole fraction - Liquid (1) 3 4.36 1 -1 1.89e-01 Relative mass - solution (1) 3 1.89 g₁/100 g sln 1 4.28e+01 Ambient temperature 3 4.28 °C 10 -4 4.61e-04 Mole fraction - Liquid (1) 3 4.61 1 -1 2.00e-01 Relative mass - solution (1) 3 2.00 g₁/100 g sln 1 Solubility, Solubility data series A round-bottmed flask containing about 4 mL of (1) and 400 mL of (2) was evacuated, suspended in a thermostat, shaken for 24h and then allowed to settle for at least another 24h. Next, desired quantities of the water layer were syphoned into 6 glass-stoppered Erlenmeyer flasks. These 6 flasks had previously been tared, partially filled with a suitable amount of diluent water, and reweighed. Weighed portions of the samples were inserted into a quartz cuvette and measured in a Beckman DU spectrophotometer. Absorbances were corrected for absorption of (1) onto the walls of the cuvette. The International Union of Pure and Applied Chemistry Bohon, R. L.; Claussen, W. F.; J. Am. Chem. Soc. 1951, 73, 1571-8. paper https://doi.org/10.1021/ja01148a047 7732-18-5 2 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Water Air-free conductivity water, no other details given. 71-43-2 1 C6H6 InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H UHOVQNZJYSORNB-UHFFFAOYSA-N 78.1118 Benzene Baker and Adamson, purified by recrystallization from ethanol, washing, filtering through silica gel then distilling. Purity was determined by refractometry (no values given). Benzene with Water