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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 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]
The primary advantages of Fischer esterification compared to other esterification processes are based on its relative simplicity. Straightforward acidic conditions can be used if acid-sensitive functional groups are not an issue; sulfuric acid can be used; weaker acids can be used with a tradeoff of longer reaction times.
It adopts a face-sharing bioctahedral structure with a Nb(III)=Nb(III) bond, spanned by two chloride and one dimethylsulfide ligands. The complex Pt 2 Me 4 (μ-SMe 2 ) 2 is a source of "PtMe 2 ". [ 10 ]
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Oxychlorination is employed in the conversion of ethylene into vinyl chloride. In the first step in this process, ethylene undergoes oxychlorination to give ethylene chloride: CH 2 =CH 2 + 2 HCl + ½ O 2 → ClCH 2 CH 2 Cl + H 2 O. Oxychlorination is of special importance in the making of 1,2-dichloroethane, which is then converted into vinyl ...