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  2. tert-Butyl chloride - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_chloride

    (ch 3) 3 coh + hcl → (ch 3) 3 ccl + h 2 o Because tert -butanol is a tertiary alcohol, the relative stability of the tert -butyl carbocation in the step 2 allows the S N 1 mechanism to be followed, whereas a primary alcohol would follow an S N 2 mechanism.

  3. Isobutyl chloride - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_chloride

    Hazard statements. H225: Precautionary statements. P210: Flash point: ... Isobutyl chloride (1-chloro-2-methylpropane) is an organochlorine compound.

  4. Butyl chloride - Wikipedia

    en.wikipedia.org/wiki/Butyl_chloride

    Isobutyl chloride (1-chloro-2-methylpropane) tert-Butyl chloride (2-chloro-2-methylpropane) This page was last edited on 25 November ...

  5. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    For example, the industrial production of chloroethane proceeds by the reaction of ethylene with HCl: 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.

  6. Methylchloroisothiazolinone - Wikipedia

    en.wikipedia.org/wiki/Methylchloroisothiazolinone

    In pure form or in high concentrations, methylchloroisothiazolinone is a skin and membrane irritant and causes chemical burns. In the United States, maximum authorized concentrations are 15 ppm in rinse-offs (of a mixture in the ratio 3:1 of 5-chloro-2-methylisothiazol 3(2H)-one and 2-methylisothiazol-3 (2H)-one). [6]

  7. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    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.

  8. Chlormethine - Wikipedia

    en.wikipedia.org/wiki/Chlormethine

    The effect of vesicant (blister) agents in the form of mustard gas (sulfur mustard, Bis(2-chloroethyl) sulfide) on bone marrow and white blood cells had been known since the First World War. [16] In 1935 several lines of chemical and biological research yielded results that would be explored after the start of the Second World War.

  9. Indoxacarb - Wikipedia

    en.wikipedia.org/wiki/Indoxacarb

    Indoxacarb is the active ingredient in a number of household insecticides, including cockroach and ant baits, and can remain active after digestion. [10] In 2012 DuPont's Professional Products including the line of Advion and Arilon products was purchased by Syngenta. [11]

  1. Related searches 2-chloro-2-methylpropane hazards information examples solution side effects

    chloro 2 methylpropane sdsmethylpropane sds sheet