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DCM is produced by treating either chloromethane or methane with chlorine gas at 400–500 °C. At these temperatures, both methane and chloromethane undergo a series of reactions producing progressively more chlorinated products.
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.
Ethylene dichloride (EDC) Methylene chloride: Methyl ethyl ketone (MEK) Vinyl trichloride: Polycarbonate (PC) Ethylene dichloride (EDC) Methylene chloride: Methyl ethyl ketone (MEK) Polystyrene (PS) Acetone: Ethylene dichloride (EDC) Methylene chloride: Methyl ethyl ketone (MEK) Toluene: Xylene: Polyvinyl chloride (PVC) Acetone: Cyclohexane ...
Phase behavior Triple point? K (? °C), ? Pa Critical point [6]: 510 K (237 °C), 6100 kPa Std enthalpy change of fusion, Δ fus H o +6.160 kJ/mol Std entropy change
Rochow's synthesis involved passing methyl chloride through a heated tube packed with ground silicon and copper(I) chloride. [2] The current industrial method places finely ground silicon in a fluidized bed reactor at about 300 °C.
Dichloroacetic acid (DCA), sometimes called bichloroacetic acid (BCA), is the organic compound with formula CHCl 2 CO 2 H.It is an analogue of acetic acid, in which 2 of the 3 hydrogen atoms of the methyl group have been replaced by chlorine atoms.
Methanesulfonyl chloride is mainly used to give methanesulfonates by its reaction with alcohols in the presence of a non-nucleophilic base. [8] In contrast to the formation of toluenesulfonates from alcohols and p-toluenesulfonyl chloride in the presence of pyridine, the formation of methanesulfonates is believed to proceed via a mechanism wherein methanesulfonyl chloride first undergoes an ...
Dichlorocarbene is an intermediate in the carbylamine reaction.In this conversion, a dichloromethane solution of a primary amine is treated with chloroform and aqueous sodium hydroxide in the presence of catalytic amount of the phase-transfer catalyst.