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  2. 3,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/3,3-Dimethylpentane

    A method to produce 3,3-dimethylpentane is to react tert-amyl chloride (CH 3 CH 2 (CH 3)C 2 Cl) with propionaldehyde producing 3,3-dimethylpentan-2-ol. This is then dehydrated to produce 3,3-dimethylpent-2-ene, which when hydrogenated produces some 3,3-dimethylpentane, but also 2,3-dimethylpentane. [2]

  3. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    The boiling point of 89.7 °C is 0.3 °C higher than the value of 89.4 °C predicted by Wiener's formula, based on the structure of the molecule and the boiling point of n-heptane. [2] [3] The speed of sound at 3 MHz is 1149.5 m/s at 20 °C and 889.5 m/s at 80 °C. [7] [8] [9]

  4. 2,2-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylpentane

    2,2-Dimethylpentane can form a clathrate hydrate with helper gas molecules. The type of clathrate formed is called "clathrate H". 2,2-Dimethylpentane was the first compound for which the structure was determined. The clathrate has 34 molecules of water per molecule, and also has xenon and hydrogen sulfide as helper molecules.

  5. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    The branched isomers are 2-methylbut-1-ene, 3-methylbut-1-ene (isopentene), and 2-methylbut-2-ene (isoamylene). Isoamylene is one of the three main byproducts of deep catalytic cracking (DCC), which is very similar to the operation of fluid catalytic cracking (FCC).

  6. 1,2,3,4,5-Pentakis (4-butylphenyl)-1,3-cyclopentadiene ...

    en.wikipedia.org/wiki/1,2,3,4,5-Pentakis(4-butyl...

    1,2,3,4,5-Pentakis(4-butylphenyl)-1,3-cyclopentadiene is an organochemical compound from the diene group and a cyclopentadiene derivative. The anion of this compound is used as a sterically demanding ligand, often abbreviated as Cp [BIG] , in the organometallic chemistry of sandwich compounds .

  7. 2,4-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,4-Dimethylpentane

    2,4-Dimethylpentane is an alkane with the chemical formula [(H 3 C) 2 CH] 2 CH 2. This colorless hydrocarbon is produced in large quantities in oil refineries. It results from the alkylation of isobutane by propylene. [1] Often referred to as "alkylate", it is blended with other gasoline components to give a high octane fuel.

  8. Tetramethylethylene - Wikipedia

    en.wikipedia.org/wiki/Tetramethylethylene

    It can be prepared by base-catalyzed isomerization of 2,3-dimethyl-1-butene. [2] Another route involves direct dimerization of propylene. [3] It can also be produced by photolysis of tetramethylcyclobutane-1,3-dione. [4]

  9. 2,3,4-Trimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3,4-Trimethylpentane

    Download as PDF; Printable version; In other projects Wikimedia Commons; ... Appearance. move to sidebar hide. 2,3,4-Trimethylpentane Skeletal formula of 2,3,4 ...