Marie C. Haulait-Pirson 2 2.7826e+02 Ambient temperature 5 2.7826 $\pu{K}$ -5 6.141e-05 Mole fraction - Liquid (1) 4 6.141 1 -2 2.800e-02 Relative mass - solution (2) 4 2.800 g₁/100 g₂ 1 2 2.8836e+02 Ambient temperature 5 2.8836 $\pu{K}$ -5 6.546e-05 Mole fraction - Liquid (1) 4 6.546 1 -2 2.985e-02 Relative mass - solution (2) 4 2.985 g₁/100 g₂ 2 2 2.9826e+02 Ambient temperature 5 2.9826 $\pu{K}$ -5 6.557e-05 Mole fraction - Liquid (1) 4 6.557 1 -2 2.990e-02 Relative mass - solution (2) 4 2.990 g₁/100 g₂ 3 2 3.0836e+02 Ambient temperature 5 3.0836 $\pu{K}$ -5 6.634e-05 Mole fraction - Liquid (1) 4 6.634 1 -2 3.025e-02 Relative mass - solution (2) 4 3.025 g₁/100 g₂ 4 2 3.1836e+02 Ambient temperature 5 3.1836 $\pu{K}$ -5 6.809e-05 Mole fraction - Liquid (1) 4 6.809 1 -2 3.105e-02 Relative mass - solution (2) 4 3.105 g₁/100 g₂ 5 1 Solubility, Solubility data series 10 mL of (2) were placed along with 4-10 drops (1) in 10 mL serum bottles, which were then tightly capped, and placed in the rotating basket and rotated for 24 hours. The bottles were then hand shaken to remove (1) droplets from the stoppers and then replaced in the bath with tops down for an additional 24 hours. The solute concentrations were determined by use of a flame-ionization gas chromatograph. Many details about equipment, operating conditions and calculation are given in the paper. The International Union of Pure and Applied Chemistry Pierotti, R. A.; Liabastre, A. A.; "Structure and properties of water solutions. " U. S. Nat. Tech. Inform. Serv.; PB Rep.; 1972, No. 21163, 113 p. report 110-83-8 1 C6H10 InChI=1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2 HGCIXCUEYOPUTN-UHFFFAOYSA-N 82.1436 Cyclohexene Eastman Organic Chemicals, No. 1043; washed with water to remove stabilizing agent. 7732-18-5 2 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Water laboratory distilled water Cyclohexene with Water