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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]
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.
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 Williamson reaction is of broad scope, is widely used in both laboratory and industrial synthesis, and remains the simplest and most popular method of preparing ethers. Both symmetrical and asymmetrical ethers are easily prepared. The intramolecular reaction of halohydrins in particular, gives epoxides.
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 ...
Stephen aldehyde synthesis, a named reaction in chemistry, was invented by Henry Stephen (OBE/MBE).This reaction involves the preparation of aldehydes (R-CHO) from nitriles (R-CN) using tin(II) chloride (SnCl 2), hydrochloric acid (HCl) and quenching the resulting iminium salt ([R-CH=NH 2] + Cl −) with water (H 2 O).
First, the mixture is treated with anhydrous hydrogen chloride in a Pinner reaction, producing crystals of acetimido ethyl ether hydrochloride: H 3 C−C≡N + C 2 H 5 OH + HCl → H 3 C−C(=NH·HCl)−OC 2 H 5. The imino ether salt is then treated with an excess of ammonia in dry ethanol, converting the ether to the amidine:
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 ...