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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

    1-Chloro-2-methylpropane. ... Hazard statements. H225: Precautionary statements. ... This page was last edited on 3 September 2024, at 20:38 (UTC).

  4. Butyl chloride - Wikipedia

    en.wikipedia.org/wiki/Butyl_chloride

    tert-Butyl chloride (2-chloro-2-methylpropane) Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.

  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 + 12 O 2 → ClCH 2 CH 2 Cl + H 2 O.

  6. Isobutylene - Wikipedia

    en.wikipedia.org/wiki/Isobutylene

    Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula (CH 3) 2 C=CH 2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene . It is a colorless flammable gas, and is of considerable industrial value.

  7. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert -butyl group attached to a bromide substituent.

  8. 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]

  9. Isopropyl chloride - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_chloride

    Isopropyl chloride is an organic compound with the chemical formula (CH 3) 2 CHCl. It is a colourless to slightly yellow, volatile, flammable liquid with a sweet, ether-like (almost like petroleum) odour. It is used as an industrial solvent. It is produced industrially by the addition of HCl to propylene: [1] CH 3 CH=CH 2 + HCl → (CH 3) 2 CHCl