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Trichloroethylene (TCE) is a halocarbon with the formula C 2 HCl 3, commonly used as an industrial metal degreasing solvent. It is a clear, colourless, non-flammable, volatile liquid with a chloroform-like pleasant mild smell [3] and sweet taste. [9] Its IUPAC name is trichloroethene. Trichloroethylene has been sold under a variety of trade names.
1,1,2-Trichloroethane, vinyl trichloride or 1,1,2-TCA, is an organochloride solvent with the molecular formula C 2 H 3 Cl 3 and the structural formula CH 2 Cl—CHCl 2.It is a colourless, sweet-smelling liquid that does not dissolve in water, but is soluble in most organic solvents.
Others from this series were Perklone (Tetrachloroethylene), Triklone (Trichloroethylene), Methoklone (Dichloromethane) and Genklene (1,1,1-Trichloroethane). [15] [16] CFC-113 is one of the three most popular CFCs, along with CFC-11 and CFC-12. [17] CFC-113 in laboratory analytics has been replaced by other solvents. [18]
1,1,1-Trichloroethane is an excellent solvent for many organic compounds and also one of the least toxic of the chlorinated hydrocarbons.It is generally considered non-polar, but owing to the good polarizability of the chlorine atoms, it is a superior solvent for organic compounds that do not dissolve well in hydrocarbons such as hexane.
This reaction was the first example of a carbon-carbon bond-forming reaction that followed a Pd(0)/Pd(II) catalytic cycle, the same catalytic cycle that is seen in other Pd(0)-catalyzed cross-coupling reactions. The Heck reaction is a way to substitute alkenes.
Trichloroethylene is a major byproduct, which is separated by distillation. Worldwide production was about 1 million metric tons (980,000 long tons; 1,100,000 short tons) in 1985. [11] Although in very small amounts, tetrachloroethylene occurs naturally in volcanoes along with trichloroethylene. [12]
Organic synthesis is an important chemical process that is integral to many scientific fields. Examples of fields beyond chemistry that require organic synthesis include the medical industry, pharmaceutical industry, and many more. Organic processes allow for the industrial-scale creation of pharmaceutical products.
Friedel–Crafts reactions have been used in the synthesis of several triarylmethane and xanthene dyes. [26] Examples are the synthesis of thymolphthalein (a pH indicator) from two equivalents of thymol and phthalic anhydride: A reaction of phthalic anhydride with resorcinol in the presence of zinc chloride gives the fluorophore fluorescein.