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  2. Acetylene - Wikipedia

    en.wikipedia.org/wiki/Acetylene

    Acetylene (systematic name: ethyne) is the chemical compound with the formula C 2 H 2 and structure H−C≡C−H. It is a hydrocarbon and the simplest alkyne. [8] This colorless gas is widely used as a fuel and a chemical building block. It is unstable in its pure form and thus is usually handled as a solution. [9]

  3. 2-Butyne - Wikipedia

    en.wikipedia.org/wiki/2-butyne

    Symmetry analysis using the Molecular Symmetry Group [4] [5] G 36 shows that one would need to analyse its high resolution rotation-vibration Raman spectrum to determine its equilibrium structure. 2-Butyne (dimethylethyne) forms with 5-decyne (dibutylethyne), 4-octyne (dipropylethyne) and 3-hexyne (diethylethyne) a group of symmetric alkynes.

  4. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    The π-bond in the ethylene molecule is responsible for its useful reactivity. The double bond is a region of high electron density, thus it is susceptible to attack by electrophiles. Many reactions of ethylene are catalyzed by transition metals, which bind transiently to the ethylene using both the π and π* orbitals. [citation needed]

  5. Propyne - Wikipedia

    en.wikipedia.org/wiki/Propyne

    In propyne, these two signals have almost exactly the same chemical shifts, leading to overlap of the signals, and the 1 H NMR spectrum of propyne, when recorded in deuteriochloroform on a 300 MHz instrument, consists of a single signal, a sharp singlet resonating at 1.8 ppm.

  6. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    A 3D model of ethyne (), the simplest alkyneIn organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. [1] The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula C n H 2n−2.

  7. 1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-dichloroethylene

    1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2.The two compounds are isomers, each being colorless liquids with a sweet odor.

  8. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    In ethene, the two carbon atoms form a σ bond by overlapping one sp 2 orbital from each carbon atom. The π bond between the carbon atoms perpendicular to the molecular plane is formed by 2p–2p overlap. Each carbon atom forms covalent C–H bonds with two hydrogens by s–sp 2 overlap, all with 120° bond angles. The hydrogen–carbon bonds ...

  9. Silver acetylide - Wikipedia

    en.wikipedia.org/wiki/Silver_acetylide

    The compound can be regarded as a silver salt of the weak acid, acetylene. The salt's anion consists of two carbon atoms linked by a triple bond, thus, its structure is [Ag +] 2 [− C≡C −]. The alternate name "silver carbide" is rarely used, although the analogous calcium compound CaC 2 is called calcium carbide. Silver acetylide is a ...

  1. Related searches draw the structure of ethyne that forms the following acid bond with two

    double bond of ethyleneacetylene bonds
    p bond of ethyleneethylene hydrocarbons