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  2. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    2 Alkenes. Toggle the table of contents. ... Download as PDF; Printable version; In other projects ... By using this site, ...

  3. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    C 2 H 6: C 2 H 4: C 2 H 2: Class alkane: alkane: alkene: alkyne: Structure Hybridisation of carbon sp 3: sp 3: sp 2: sp C-H bond length 1.087 Å: 1.094 Å: 1.087 Å: 1.060 Å: Proportion of ethane C-H bond length 99% 100% 99% 97% Structure determination method microwave spectroscopy: microwave spectroscopy microwave spectroscopy infrared ...

  4. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    In acetylene, the H–C≡C bond angles are 180°. By virtue of this bond angle, alkynes are rod-like. Correspondingly, cyclic alkynes are rare. Benzyne cannot be isolated. . The C≡C bond distance of 118 picometers (for C 2 H 2) is much shorter than the C=C distance in alkenes (132 pm, for C 2 H 4) or the C–C bond in alkanes (153 p

  5. Category:Alkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkanes

    Download as PDF; Printable version; ... An alkane is an acyclic saturated hydrocarbon. See Alkane. ... By using this site, ...

  6. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    CH 4 + O 22 H 2 O + C. See the alkane heat of formation table for detailed data. The standard enthalpy change of combustion, Δ c H ⊖, for alkanes increases by about 650 kJ/mol per CH 2 group. Branched-chain alkanes have lower values of Δ c H ⊖ than straight-chain alkanes of the same number of carbon atoms, and so can be seen to be ...

  7. 1-Decyne - Wikipedia

    en.wikipedia.org/wiki/1-Decyne

    1-Decyne is the organic compound with the formula C 8 H 17 C≡CH. It is a terminal alkyne.A colorless liquid, 1-decyne is used as a model substrate when evaluating methodology in organic synthesis.

  8. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ] [ 2 ] Number of C atoms

  9. Alkyne trimerisation - Wikipedia

    en.wikipedia.org/wiki/Alkyne_trimerisation

    An alkyne trimerisation is a [2+2+2] cycloaddition reaction in which three alkyne units (C≡C) react to form a benzene ring. The reaction requires a metal catalyst. The process is of historic interest as well as being applicable to organic synthesis. [1] Being a cycloaddition reaction, it has high atom economy.