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  2. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F). It is widely used as a cheap, relatively safe, largely unreactive, and easily evaporated non-polar solvent, and modern gasoline blends contain about 3% hexane. [8]

  3. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    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 hydride ...

  4. 3-Hexyne - Wikipedia

    en.wikipedia.org/wiki/3-Hexyne

    3-Hexyne is the organic compound with the formula C 2 H 5 CCC 2 H 5. This colorless liquid is one of three isomeric hexynes. 3-Hexyne forms with 5-decyne, 4-octyne, and 2-butyne a series of symmetric alkynes. It is a reagent in organometallic chemistry. [1] Structure of the coordination complex NbCl 3 (dimethoxyethane)(3-hexyne). [2]

  5. Hexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Hexane_(data_page)

    van der Waals' constants [3] a = 2471 L 2 kPa/mol 2 b = 0.1735 liter per mole Vapor pressure of liquid ... log 10 of Hexane vapor pressure. Uses formula: ...

  6. C6H14 - Wikipedia

    en.wikipedia.org/wiki/C6H14

    3-Methylpentane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  7. 3-Methylhexane - Wikipedia

    en.wikipedia.org/wiki/3-Methylhexane

    3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane . The molecule is chiral , and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane .

  8. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    The former result from the overlap of an sp 3 orbital of carbon with the 1s orbital of a hydrogen; the latter by the overlap of two sp 3 orbitals on adjacent carbon atoms. The bond lengths amount to 1.09 × 10 −10 m for a C–H bond and 1.54 × 10 −10 m for a C–C bond.

  9. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    3,3-dimethylbut-1-yne This page was last edited on 22 May 2021, at 18:45 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...