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  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 differences between cis and trans isomers can be larger if polar bonds are present, as in the 1,2-dichloroethenes. 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 ...

  4. 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.

  5. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    It is opposed to stereoisomerism, in which the atoms and bonding scheme are the same, but only the relative spatial arrangement of the atoms is different. [5] [6] Examples of the latter are the enantiomers, whose molecules are mirror images of each other, and the cis and trans versions of 2-butene.

  6. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    The most stable trans-isomers of 10 ring or greater cycloalkenes exhibit 4 irregularities from standard geometric norms. The first irregularity is twisted planes of substituents along the C=C. Using C=C as the stable axis, 2 substituents of 1 carbon can be visualized on the same plane, equally applied to the other carbon.

  7. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    The most common one in nature (myo-inositol) has the hydroxyls on carbons 1, 2, 3 and 5 on the same side of that plane, and can therefore be called cis-1,2,3,5-trans-4,6-cyclohexanehexol. And each of these cis - trans isomers can possibly have stable "chair" or "boat" conformations (although the barriers between these are significantly lower ...

  8. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    Other organic compounds have the formula C 4 H 8, namely cyclobutane and methylcyclopropane, but are not alkenes and do not fall under the name butene. There are also cyclic alkenes with four carbon atoms overall such as cyclobutene and two isomers of methylcyclopropene, but they do not have the formula C 4 H 8 and are not discussed here.

  9. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Number of C atoms Number of isomers [3] [4] 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 ...