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  2. Cyclobutane - Wikipedia

    en.wikipedia.org/wiki/Cyclobutane

    Cyclobutane is a cycloalkane and organic compound with the formula (CH 2) 4. Cyclobutane is a colourless gas and is commercially available as a liquefied gas. Derivatives of cyclobutane are called cyclobutanes. Cyclobutane itself is of no commercial or biological significance, but more complex derivatives are important in biology and ...

  3. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Ball-and-stick model of cyclobutane In organic chemistry , the cycloalkanes (also called naphthenes , but distinct from naphthalene ) are the monocyclic saturated hydrocarbons . [ 1 ] In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains ), and all of ...

  4. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Acyclic aliphatic/non-aromatic compound Cyclic aliphatic/non-aromatic compound (cyclobutane)In organic chemistry, hydrocarbons (compounds composed solely of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (/ ˌ æ l ɪ ˈ f æ t ɪ k /; G. aleiphar, fat, oil).

  5. Category:Cyclobutanes - Wikipedia

    en.wikipedia.org/wiki/Category:Cyclobutanes

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  6. Butane - Wikipedia

    en.wikipedia.org/wiki/Butane

    Normal butane can be used for gasoline blending, as a fuel gas, fragrance extraction solvent, either alone or in a mixture with propane, and as a feedstock for the manufacture of ethylene and butadiene, a key ingredient of synthetic rubber. Isobutane is primarily used by refineries to enhance (increase) the octane number of motor gasoline.

  7. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    Cycloalkanes, the simplest carbocycles, including cyclopropane, cyclobutane, cyclopentane, and cyclohexane. Note, elsewhere an organic chemistry shorthand is used where hydrogen atoms are inferred as present to fill the carbon's valence of 4 (rather than their being shown explicitly).

  8. Thorpe–Ingold effect - Wikipedia

    en.wikipedia.org/wiki/Thorpe–Ingold_effect

    An example of this is an olefin metathesis reaction: [4] In the field of peptide foldamers, amino acid residues containing quaternary carbons such as 2-aminoisobutyric acid are used to promote formation of certain types of helices. [5] One proposed explanation for this effect is that the increased size of the substituents increases the angle ...

  9. Cyclobutanes - Wikipedia

    en.wikipedia.org/?title=Cyclobutanes&redirect=no

    This page was last edited on 15 May 2006, at 07:29 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply ...