Search results
Results from the WOW.Com Content Network
[1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.
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.
CH 4 + Cl 2 → CH 3 Cl + HCl CH 3 Cl + Cl 2 → CH 2 Cl 2 + HCl CH 2 Cl 2 + Cl 2 → CHCl 3 + HCl CHCl 3 + Cl 2 → CCl 4 + HCl. The output of these processes is a mixture of chloromethane, dichloromethane, chloroform, and carbon tetrachloride as well as hydrogen chloride as a byproduct. These compounds are separated by distillation.
Most compounds considered to be Lewis acids require an activation step prior to formation of the adduct with the Lewis base. Complex compounds such as Et 3 Al 2 Cl 3 and AlCl 3 are treated as trigonal planar Lewis acids but exist as aggregates and polymers that must be degraded by the Lewis base. [10] A simpler case is the formation of adducts ...
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 ...
Structure and properties Index of refraction, [1] n D: 1.4448 Abbe number? Dielectric constant, [2] ε r: 10.5 ε 0 at 20 °C Bond strength? Bond length? Bond angle? Magnetic susceptibility? Surface tension [3] 40.05 mN/m at 10 °C 38.75 mN/m at 20 °C 28.4 mN/m at 100 °C Viscosity [4] 1.1322 mPa·s at 0 °C 0.8385 mPa·s at 20 °C 0.6523 mPa ...
Benzyl chloride is prepared industrially by the gas-phase photochemical reaction of toluene with chlorine: [3] C 6 H 5 CH 3 + Cl 2 → C 6 H 5 CH 2 Cl + HCl. In this way, approximately 100,000 tonnes are produced annually. The reaction proceeds by the free radical process, involving the intermediacy of free chlorine atoms. [4]
In this way, the anti-Markovnikov product is obtained. [2] Alternatively, n‑propanol may be substitutively brominated. [3] The latter reaction is also viable laboratory synthesis. One laboratory technique for substitutive bromination treats propanol with a mixture of hydrobromic and sulfuric acids: CH 3 CH 2 CH 2 OH + HBr → CH 3 CH 2 CH 2 ...