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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. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2.It is a colourless, flammable gas with a faint "sweet and musky" odour when pure. [7] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds).

  4. 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.

  5. Propyne - Wikipedia

    en.wikipedia.org/wiki/Propyne

    Propyne has been detected in multiple astrophysical objects following its first observation in 1973 in the galactic center giant molecular cloud Sgr B2 using radio astronomy techniques. [11] Propyne has been proposed to act as a precursor molecule to the formation of PAHs in space, such as indene .

  6. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    This colourless gas has a strong ammonia-like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines. Ethylamine is widely used in chemical industry and organic synthesis. [4] It is a DEA list I chemical by 21 CFR § 1310.02.

  7. Alkynylation - Wikipedia

    en.wikipedia.org/wiki/Alkynylation

    In organic chemistry, alkynylation is an addition reaction in which a terminal alkyne (−C≡CH) is added to a carbonyl group (C=O) to form an α-alkynyl alcohol (R 2 C(−OH)−C≡C−R). [1] [2] When the acetylide is formed from acetylene (HC≡CH), the reaction gives an α-ethynyl alcohol. This process is often referred to as ethynylation.

  8. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    Hydration is an important process in many other applications; one example is the production of Portland cement by the crosslinking of calcium oxides and silicates that is induced by water. Hydration is the process by which desiccants function. CuSO 4 ·5H 2 O is bright blue and has a rather different structure from its colourless anhydrous ...

  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 ...

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