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  2. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    A 3D model of ethyne , the simplest alkyne. In 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.

  3. 2-Butyne - Wikipedia

    en.wikipedia.org/wiki/2-butyne

    2-Butyne (dimethylacetylene, crotonylene or but-2-yne) is an alkyne with chemical formula CH 3 C≡CCH 3.Produced artificially, it is a colorless, volatile, pungent liquid at standard temperature and pressure.

  4. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    With aqueous pK a values of around 16–19, alcohols are, in general, slightly weaker acids than water. With strong bases such as sodium hydride or sodium they form salts [a] called alkoxides, with the general formula RO − M + (where R is an alkyl and M is a metal). R−OH + NaH → R−O − Na + + H 2 2 R−OH + 2 Na → 2 R−O − Na + + H 2

  5. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    In chemistry, a hydration reaction is a chemical reaction in which a substance combines with water. In organic chemistry, water is added to an unsaturated substrate, which is usually an alkene or an alkyne. This type of reaction is employed industrially to produce ethanol, isopropanol, and butan-2-ol. [1]

  6. 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]

  7. Sodium amide - Wikipedia

    en.wikipedia.org/wiki/Sodium_amide

    Usually two equivalents of sodium amide yields the desired alkyne. Three equivalents are necessary in the preparation of a terminal alkynes because the terminal CH of the resulting alkyne protonates an equivalent amount of base. Hydrogen chloride and ethanol can also be eliminated in this way, [11] as in the preparation of 1-ethoxy-1-butyne. [12]

  8. Cycloalkyne - Wikipedia

    en.wikipedia.org/wiki/Cycloalkyne

    Cycloalkynes have a general formula C n H 2n−4. Because of the linear nature of the C−C≡C−C alkyne unit, cycloalkynes can be highly strained and can only exist when the number of carbon atoms in the ring is great enough to provide the flexibility necessary to accommodate this geometry .

  9. 1-Pentyne - Wikipedia

    en.wikipedia.org/wiki/1-Pentyne

    1-Pentyne is an organic compound with the formula CH 3 CH 2 CH 2 C≡CH. It is a terminal alkyne , in fact the smallest that is liquid at room temperature. The compound is a common terminal alkyne substrate in diverse studies of catalysis.