enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/1-Butene

    1-Butene (IUPAC name: But-1-ene, also known as 1-butylene) is the organic compound with the formula CH 3 CH 2 CH=CH 2. It is a colorless gas. But-1-ene is an alkene easily condensed to give a colorless liquid. It is classified as a linear alpha-olefin (terminal alkene). [2] It is one of the isomers of butene (butylene). It is a precursor to ...

  3. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    The cis isomer in this case has a boiling point of 60.3 °C, while the trans isomer has a boiling point of 47.5 °C. [6] In the cis isomer the two polar C–Cl bond dipole moments combine to give an overall molecular dipole, so that there are intermolecular dipole–dipole forces (or Keesom forces), which add to the London dispersion forces and ...

  4. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride; methylethyl methane 5 3 3 C 5 H 12 ...

  5. Isobutylene - Wikipedia

    en.wikipedia.org/wiki/Isobutylene

    1-Butene cis-2-Butene trans-2-Butene: Related compounds. Isobutane: ... It is a four-carbon branched alkene (olefin), one of the four isomers of butylene. It is a ...

  6. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    Butene, also known as butylene, is an alkene with the formula C 4 H 8.The word butene may refer to any of the individual compounds. They are colourless gases that are present in crude oil as a minor constituent in quantities that are too small for viable extraction.

  7. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    Trans-alkenes are about 1 kcal/mol more stable than cis-alkenes. An example of this effect is cis- vs trans-2-butene. The difference is attributed to unfavorable non-bonded interactions in the cis isomer. Terminal alkenes isomerize to internal alkenes in the presence of metal catalysts.

  8. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For example, of the isomers of butene, the two methyl groups of (Z)-but-2-ene (a.k.a. cis-2-butene) appear on the same side of the double bond, and in (E)-but-2-ene (a.k.a. trans-2-butene) the methyl groups appear on opposite sides. These two isomers of butene have distinct properties.

  9. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Multiple double bonds take the form -diene, -triene, etc., with the size prefix of the chain taking an extra "a": CH 2 =CHCH=CH 2 is buta-1,3-diene. Simple cis and trans isomers may be indicated with a prefixed cis-or trans-: cis-but-2-ene, trans-but-2-ene. However, cis-and trans-are relative descriptors.