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Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.
Triple point: 279.48 K (6.33 °C), 5.388 kPa [3] Critical point: 554 K (281 °C), 4070 kPa Std enthalpy change of fusion, Δ fus H o: 2.68 kJ/mol crystal I → liquid Std entropy change of fusion, Δ fus S o: 9.57 J/(mol·K) crystal I → liquid Std enthalpy change of vaporization, Δ vap H o: 32 kJ/mol Std entropy change of vaporization, Δ ...
Cyclohexanone oxime can be prepared from the condensation reaction between cyclohexanone and hydroxylamine: [1]. C 5 H 10 CO + H 2 NOH → C 5 H 10 C=NOH + H 2 O. Alternatively, another industrial route involves the reaction of cyclohexane with nitrosyl chloride, which is a free-radical reaction.
Cyclohexane has two crystalline phases. The high-temperature phase I, stable between 186 K and the melting point 280 K, is a plastic crystal, which means the molecules retain some rotational degree of freedom. The low-temperature (below 186 K) phase II is ordered.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Cyclohexyl chloride can be prepared from cyclohexanol by ... This page is always in light mode. ... 118.60 g·mol −1: Density: 1 g/mL Melting point: −44 °C (− ...
Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.
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