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  2. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    Internal alkynes feature carbon substituents on each acetylenic carbon. Symmetrical examples include diphenylacetylene and 3-hexyne. They may also be asymmetrical, such as in 2-pentyne. Terminal alkynes have the formula RC≡CH, where at least one end of the alkyne is a hydrogen atom. An example is methylacetylene (propyne using IUPAC ...

  3. Transition metal alkyne complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkyne...

    Transition metal alkyne complexes are often formed by the displacement of labile ligands by the alkyne. For example, a variety of cobalt-alkyne complexes arise by the reaction of alkynes with dicobalt octacarbonyl. [2] Co 2 (CO) 8 + R 2 C 2 → (R 2 C 2)Co 2 (CO) 6 + 2 CO. Many alkyne complexes are produced by reduction of metal halides: [3]

  4. Category:Alkynes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkynes

    Alkyne derivatives (7 C, 86 P) Alkynyl groups (4 P) P. Polyynes (1 C, 9 P) Pages in category "Alkynes" The following 27 pages are in this category, out of 27 total.

  5. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    an organic compound; simplest example of the ketones: Acetylene: a hydrocarbon and the simplest alkyne; widely used as a fuel and chemical building block Ammonia: inorganic; the precursor to most nitrogen-containing compounds; used to make fertilizer Ammonium hydroxide: aqueous ammonia; used in traditional qualitative inorganic analysis

  6. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    1.557 454 318 575 50 × 10 20: 3.373 536 543 484 52 × 10 23: C 55 H 112: n-pentapentacontane: 56 4.191 495 711 934 12 × 10 20: 1.060 278 034 376 26 × 10 24: C 56 H 114: n-hexapentacontane: 57 1.128 939 578 361 33 × 10 21: 3.335 014 088 191 92 × 10 24: C 57 H 116: n-heptapentacontane: 58 3.043 043 571 906 83 × 10 21: 1.049 801 595 284 36 ...

  7. Cycloalkyne - Wikipedia

    en.wikipedia.org/wiki/Cycloalkyne

    Large alkyne-containing carbocycles may be virtually unstrained, while the smallest constituents of this class of molecules may experience so much strain that they have yet to be observed experimentally. [1] Cyclooctyne (C 8 H 12) is the smallest cycloalkyne capable of being isolated and stored as a stable compound. [2]

  8. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    The hexynes are a subgroup from the group of alkynes. It consists of several isomeric compounds having the formula C 6 H 10. The linear and branched members are: 1-Hexyne (n-butylacetylene) 2-Hexyne (methylpropylacetylene) 3-Hexyne (diethylacetylene) 3-methylpent-1-yne; 4-methylpent-1-yne; 4-methylpent-2-yne; 3,3-dimethylbut-1-yne

  9. Aryne - Wikipedia

    en.wikipedia.org/wiki/Aryne

    Arynes are examples of didehydroarenes (1,2-didehydroarenes in this case), although 1,3- and 1,4-didehydroarenes are also known. [ 3 ] [ 4 ] [ 5 ] Arynes are examples of alkynes under high strain .