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Boiling point: 102 to 103 °C (216 to 217 °F; 375 to 376 K) ... [2] [3] It can also be synthesized as a side product of the dehydration of 2-methylcyclohexanol into ...
Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: ... [2] Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80. ...
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.
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Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. Methylcyclohexane, as a component of a mixture, is usually dehydrogenated to toluene, which increases the octane rating of gasoline.
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.
Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.
In the presence of a Cinchona alkaloid, bromination of an alkene can leads to optically active dibromides. [2] For 4-methylcyclohexene, the ( S )-configuration leads to two different products: the bromines can add at the axial positions, giving the orientation (1 S ,3 R ,4 R ), or at the equatorial positions, giving the orientation (1 S ,3 S ,4 ...