M. Elizabeth Derrick, H. Lawrence Clever 2 2.7315e+02 Ambient temperature 5 2.7315 $\pu{K}$ -2 1.520e-02 Mole fraction - Liquid (1) 4 1.520 1 0 4.843e+00 Ostwald coefficient 4 4.843 1 0 4.843e+00 Bunsen Coefficient 4 4.843 $\pu{cm3(g) cm-3(l) atm-1}$ 1 2 2.7815e+02 Ambient temperature 5 2.7815 $\pu{K}$ -2 1.420e-02 Mole fraction - Liquid (1) 4 1.420 1 0 4.572e+00 Ostwald coefficient 4 4.572 1 0 4.490e+00 Bunsen Coefficient 4 4.490 $\pu{cm3(g) cm-3(l) atm-1}$ 2 2 2.8315e+02 Ambient temperature 5 2.8315 $\pu{K}$ -2 1.325e-02 Mole fraction - Liquid (1) 4 1.325 1 0 4.308e+00 Ostwald coefficient 4 4.308 1 0 4.156e+00 Bunsen Coefficient 4 4.156 $\pu{cm3(g) cm-3(l) atm-1}$ 3 2 2.8815e+02 Ambient temperature 5 2.8815 $\pu{K}$ -2 1.240e-02 Mole fraction - Liquid (1) 4 1.240 1 0 4.074e+00 Ostwald coefficient 4 4.074 1 0 3.862e+00 Bunsen Coefficient 4 3.862 $\pu{cm3(g) cm-3(l) atm-1}$ 4 2 2.9315e+02 Ambient temperature 5 2.9315 $\pu{K}$ -2 1.160e-02 Mole fraction - Liquid (1) 4 1.160 1 0 3.847e+00 Ostwald coefficient 4 3.847 1 0 3.585e+00 Bunsen Coefficient 4 3.585 $\pu{cm3(g) cm-3(l) atm-1}$ 5 2 2.9815e+02 Ambient temperature 5 2.9815 $\pu{K}$ -2 1.088e-02 Mole fraction - Liquid (1) 4 1.088 1 0 3.640e+00 Ostwald coefficient 4 3.640 1 0 3.335e+00 Bunsen Coefficient 4 3.335 $\pu{cm3(g) cm-3(l) atm-1}$ 6 2 3.0315e+02 Ambient temperature 5 3.0315 $\pu{K}$ -2 1.028e-02 Mole fraction - Liquid (1) 4 1.028 1 0 3.473e+00 Ostwald coefficient 4 3.473 1 0 3.129e+00 Bunsen Coefficient 4 3.129 $\pu{cm3(g) cm-3(l) atm-1}$ 7 2 3.0815e+02 Ambient temperature 5 3.0815 $\pu{K}$ -3 9.641e-03 Mole fraction - Liquid (1) 4 9.641 1 0 3.285e+00 Ostwald coefficient 4 3.285 1 0 2.912e+00 Bunsen Coefficient 4 2.912 $\pu{cm3(g) cm-3(l) atm-1}$ 8 2 3.1315e+02 Ambient temperature 5 3.1315 $\pu{K}$ -3 9.144e-03 Mole fraction - Liquid (1) 4 9.144 1 0 3.142e+00 Ostwald coefficient 4 3.142 1 0 2.741e+00 Bunsen Coefficient 4 2.741 $\pu{cm3(g) cm-3(l) atm-1}$ 9 1 2 2.7315e+02 Ambient temperature 5 2.7315 $\pu{K}$ -2 1.524e-02 Mole fraction - Liquid (1) 4 1.524 1 1 2 2.8315e+02 Ambient temperature 5 2.8315 $\pu{K}$ -2 1.323e-02 Mole fraction - Liquid (1) 4 1.323 1 2 2 2.8815e+02 Ambient temperature 5 2.8815 $\pu{K}$ -2 1.237e-02 Mole fraction - Liquid (1) 4 1.237 1 3 2 2.9315e+02 Ambient temperature 5 2.9315 $\pu{K}$ -2 1.160e-02 Mole fraction - Liquid (1) 4 1.160 1 4 2 2.9815e+02 Ambient temperature 5 2.9815 $\pu{K}$ -2 1.089e-02 Mole fraction - Liquid (1) 4 1.089 1 5 2 3.0315e+02 Ambient temperature 5 3.0315 $\pu{K}$ -2 1.025e-02 Mole fraction - Liquid (1) 4 1.025 1 6 2 3.1315e+02 Ambient temperature 5 3.1315 $\pu{K}$ -3 9.14e-03 Mole fraction - Liquid (1) 3 9.14 1 7 2 Solubility, Solubility data series The apparatus consists of a gas buret, a solvent reservoir, and an absorption pipet. The volume of the pipet is determined at various meniscus heights by weighing a quantity of water. The meniscus height is read with a cathetometer.<p>The dry gas is introduced into the degassed solvent. The gas and solvent are mixed with a magnetic stirrer until saturation. Care is taken to prevent solvent vapor from mixing with the solute gas in the gas buret. The volume of gas is determined from the gas buret readings, the volume of solvent is determined from the meniscus height in the absorption pipet. The International Union of Pure and Applied Chemistry Horiuti, J.; Sci. Pap. Inst. Phys. Chem. Res. (Jpn) 1931/32, 17, 125 - 256. paper 67-64-1 2 C3H6O InChI=1S/C3H6O/c1-3(2)4/h1-2H3 CSCPPACGZOOCGX-UHFFFAOYSA-N 58.0791 Acetone Acetone. Nippon Pure Chemical Co. or Merck. Extra pure grade. Recrystallized with sodium sulfite and stored over calcium chloride. Fractionated, BP (760 mmHg) = 56.09&deg;C. 74-85-1 1 C2H4 InChI=1S/C2H4/c1-2/h1-2H2 VGGSQFUCUMXWEO-UHFFFAOYSA-N 28.0532 Ethene Ethene. Prepared by dropping ethanol into orthophosphoric acid. The gas was cooled, passed through several wash solutions, dried, and fractionated from liquid air several times. Ethene with 2-Propanone or acetone