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Structure of the chloromethyl group. In organic chemistry, the chloromethyl group is a functional group that has the chemical formula −CH 2 −Cl. The naming of this group is derived from the methyl group (which has the formula −CH 3), by replacing one hydrogen atom by a chlorine atom. Compounds with this group are a subclass of the ...
c 6 h 5 ch 2 cl + 2 koh + 2 [o] → c 6 h 5 cook + kcl + h 2 o Benzyl chloride may be used in the synthesis of amphetamine-class drugs, and for this reason, sales of benzyl chloride are monitored as a List II drug precursor chemical by the US Drug Enforcement Administration .
Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.
Structure and properties Index of refraction, n D: 1.5241 Abbe number? Dielectric constant, ε r: 5.6895 at 293.2 K Bond strength? Bond length? Bond angle? Magnetic susceptibility, χ m: 69.5 x10 −6 cm 3 mol −1: Surface tension, 34.78 dyn/cm at 10°C 32.99 dyn/cm at 25°C 30.02 dyn/cm at 50°C 27.04 dyn/cm at 75°C 24.06 dyn/cm at 100°C
The half-life of this substance in terms of volatilization in the river, lagoon and lake is 2.1 h, 25 h and 18 days, respectively. [ 20 ] [ 21 ] The amount of methyl chloride in the stratosphere is estimated to be 2 × 10 6 tonnes per year, representing 20–25% of the total amount of chlorine that is emitted to the stratosphere annually.
Epichlorohydrin (abbreviated ECH) is an organochlorine compound and an epoxide.Despite its name, it is not a halohydrin.It is a colorless liquid with a pungent, garlic-like odor, moderately soluble in water, but miscible with most polar organic solvents. [4]
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H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.