Search results
Results from the WOW.Com Content Network
Chloroethane, commonly known as ethyl chloride, is a chemical compound with chemical formula CH 3 CH 2 Cl, once widely used in producing tetraethyllead, a gasoline additive. It is a colorless, flammable gas or refrigerated liquid with a faintly sweet odor. [11]
To convert from / to / ... Ethane: 5.562 0.0638 Ethanethiol: 11.39 0.08098 ... Hydrogen chloride: 3.716 0.04081 Hydrogen cyanide [2] 11.29
In the laboratory it is occasionally used as a source of chlorine, with elimination of ethene and chloride. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethane . Historically, before leaded petrol was phased out, chloroethanes were used as an additive in petrol to prevent lead buildup in engines.
The conditions for Stille's experiments differ significantly from industrial process conditions. Other studies using normal industrial Wacker conditions (except with high chloride and high copper chloride concentrations) also yielded products that inferred nucleophilic attack was an anti-addition reaction. [15]
Numerous attempts have been made to convert ethane directly to vinyl chloride. [2] Ethane, which is even more readily available than ethylene, is a potential precursor to vinyl chloride. The conversion of ethane to vinyl chloride has been demonstrated by various routes: [2] High-temperature chlorination: H 3 C−CH 3 + 2 Cl 2 → H 2 C=CHCl + 3 HCl
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]
Ethylene chloride is a chemical name that can refer to either of the following compounds: 1,2-dichloroethane: formula C 2 H 4 Cl 2: vinyl chloride: formula C 2 H 3 Cl
Here ethyl chloride reacts with potassium hydroxide, typically in a solvent such as ethanol, giving ethylene. Likewise, 1-chloropropane and 2-chloropropane give propene. Zaitsev's rule helps to predict regioselectivity for this reaction type.