enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Crotyl chloride - Wikipedia

    en.wikipedia.org/wiki/Crotyl_chloride

    1-Chloro-2-butene, 1-chlorobut-2-ene, 2-butenyl chloride, gamma-methylallyl chloride ... 90.55 g·mol −1 Appearance Liquid Density: ... Crotyl chloride is an ...

  3. Crotyl group - Wikipedia

    en.wikipedia.org/wiki/Crotyl_group

    Crotyl groups attached to R. A crotyl group is an organic functional group with the formula RCH 2 CH=CHCH 3. [1] Systematically, it is called a but-2-en-1-yl group and exhibits geometric isomerism, being either cis (Z) or trans (E).

  4. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    When 1 mole of HCl adds to 1 mole of 1,3-butadiene, in addition to the ordinarily expected product 3-chloro-1-butene, we also find 1-chloro-2-butene. Isotope labelling experiments have shown that what happens here is that the additional double bond shifts from 1,2 position to 2,3 position in some of the product.

  5. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    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.

  6. Allylic rearrangement - Wikipedia

    en.wikipedia.org/wiki/Allylic_rearrangement

    In the similar substitution of 1-chloro-3-methyl-2-butene, the secondary 2-methyl-3-buten-2-ol is produced in a yield of 85%, while that for the primary 3-methyl-2-buten-1-ol is 15%. Allylic shifts occur because the transition state is an allyl intermediate. In other respects they are similar to classical nucleophilic substitution, and admit ...

  7. 1,4-Dichlorobut-2-ene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobut-2-ene

    The first step is the liquid- or vapour-phase chlorination of butadiene to a mixture of 3,4-dichlorobut-1-ene and 1,4-dichlorobut-2-ene (both isomers). In the second step, the mixture of 1,4-dichlorobut-2-ene and 3,4-dichlorobut-1-ene is isomerized to 3,4-dichlorobut-1-ene by heating to temperatures of 60–120 °C in the presence of a catalyst.

  8. 1,4-Dichlorobutane - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobutane

    1,4-Dichlorobutane is a chloroalkane with the molecular formula (CH 2 CH 2 Cl) 2. It is one of several structural isomers of dichlorobutane. They are all colorless liquids of low flammabiltity and of interest for specialized synthetic uses.

  9. List of gases - Wikipedia

    en.wikipedia.org/wiki/List_of_gases

    1-Chloro-1,1,2,2-tetrafluoropropane [125] CF 2 ClCF 2 CH 3: 20 150.5 421-75-0 Perfluorooxaspiro[2.3]hexane [87] C 5 F 8 O 18-21 228 pentafluoroethylsulfinyl fluoride [71] C 2 F 5 S(O)F 20 186 20621-31-2 3-Methyl-1-butene: CH 2 =CHCH(CH 3) 2: 20.1 −168.41 70 563-45-1 Acetaldehyde: CH 3 CHO 20.2 −123.37 44 75-07-0 Chlorotetrafluoro ...