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  2. Chlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Chlorotoluene

    A laboratory route to 2- and 4-chlorotoluene proceeds from 2- and 4-toluidines (i.e. 2- and 4-aminotoluene). These compounds are diazotized followed by treatment with cuprous chloride. [1] Industrially, the diazonium method is reserved for 3-chlorotoluene. The industrial route to 2- and 4-chlorotoluene entails direct reaction of toluene with ...

  3. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl chloride, or α-chlorotoluene, is an organic compound with the formula C 6 H 5 CH 2 Cl. This colorless liquid is a reactive organochlorine compound that is a widely used chemical building block .

  4. Alkylidene group - Wikipedia

    en.wikipedia.org/wiki/Alkylidene_group

    For example, the isopropyl group (IUPAC: prop-2-yl) −CH(CH 3) 2 corresponds to the isopropylidene group =C(CH 3) 2 (IUPAC: prop-2-ylidene). The group is not typically used in common names of branched alkenes - e.g. 3-methylenepentane, the simplest compound that systematically includes an alkylidene group, [Note 1] is commonly known as 2-ethyl ...

  5. o-Toluidine - Wikipedia

    en.wikipedia.org/wiki/O-Toluidine

    o-Toluidine (ortho-toluidine) is an organic compound with the chemical formula CH 3 C 6 H 4 NH 2. It is the most important of the three isomeric toluidines . It is a colorless liquid although commercial samples are often yellowish.

  6. Laboratory safety - Wikipedia

    en.wikipedia.org/wiki/Laboratory_safety

    Many laboratories contain significant risks, and the prevention of laboratory accidents requires great care and constant vigilance. [1] [2] Examples of risk factors include high voltages, high and low pressures and temperatures, corrosive and toxic chemicals and chemical vapours, radiation, fire, explosions, and biohazards including infective organisms and their toxins.

  7. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    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. In the laboratory, the related reaction involving zinc chloride in concentrated ...

  8. Photochlorination - Wikipedia

    en.wikipedia.org/wiki/Photochlorination

    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 ...

  9. 2-Chlorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobenzoic_acid

    2-Chlorobenzoic acid is an organic compound with the formula ClC 6 H 4 CO 2 H. It is one of three isomeric chlorobenzoic acids , the one that is the strongest acid. This white solid is used as a precursor to a variety of drugs, food additives, and dyes.