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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]
The chemical compound 1,2-dichloroethane, commonly known as ethylene dichloride (EDC), is a chlorinated hydrocarbon. It is a colourless liquid with a chloroform -like odour . The most common use of 1,2-dichloroethane is in the production of vinyl chloride , which is used to make polyvinyl chloride (PVC) pipes, furniture and automobile ...
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.
Iron(III) chloride is produced commercially by oxychlorination (and other methods). For example, dissolution of iron ores in hydrochloric acid gives a mixture of ferrous and ferric chlorides: [4] Fe 3 O 4 + 8 HCl → FeCl 2 + 2 FeCl 3 + 4 H 2 O. The iron(II) chloride is converted to the iron(III) derivative by treatment with oxygen and ...
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
Tetraethyllead was produced from ethyl chloride and a sodium–lead alloy: [11] [12] 4 NaPb + 4 CH 3 CH 2 Cl → Pb(CH 3 CH 2 ) 4 + 4 NaCl + 3 Pb Reductive dechlorination is rarely useful in chemical synthesis, but is a key step in the biodegradation of several organochlorine persistent pollutants .
The major products were ethyl chloride, tetrachlorocarbon and dichloromethane. [7] Because of concerns about health and environmentally relevant problems such as the ozone depletion behavior of light volatile chlorine compounds, the chemical industry developed alternative procedures that did not require chlorinated compounds. As a result of the ...
Extractive distillation with water removes the lights ends having lower boiling points than acetaldehyde (chloromethane, chloroethane, and carbon dioxide) at the top, while water and higher-boiling byproducts, such as acetic acid, crotonaldehyde or chlorinated acetaldehydes, are withdrawn together with acetaldehyde at the bottom. [27]