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  2. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen. This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers. They are produced on a large scale for many applications.

  3. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Ethylene oxide is an organic compound with the formula C 2 H 4 O. It is a cyclic ether and the simplest epoxide: a three-membered ring consisting of one oxygen atom and two carbon atoms. Ethylene oxide is a colorless and flammable gas with a faintly sweet odor.

  4. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    A cyclic ether and high-boiling solvent (b.p. 101.1 °C). Tetrahydrofuran (THF) A cyclic ether, one of the most polar simple ethers that is used as a solvent. Anisole (methoxybenzene) An aryl ether and a major constituent of the essential oil of anise seed. Crown ethers: Cyclic polyethers that are used as phase transfer catalysts. Polyethylene ...

  5. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    The general chemical equation for the hydration of alkenes is the following: RRC=CH 2 + H 2 O → RRC(OH)-CH 3. A hydroxyl group (OH −) attaches to one carbon of the double bond, and a proton (H +) adds to the other. The reaction is highly exothermic. In the first step, the alkene acts as a nucleophile and attacks the proton, following ...

  6. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    The molecular formula C 3 H 6 O may refer to: Chemistry portal; ... Ethers. methyl vinyl ether or ... -methyl oxirane, CAS number 16088-62-3

  7. Cyclohexene oxide - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene_oxide

    Cyclohexene oxide is produced in epoxidation reaction from cyclohexene. The epoxidation can take place either in a homogeneous reaction by peracids [2] or heterogeneous catalysis (e.g. silver and molecular oxygen).

  8. Ring-opening polymerization - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_polymerization

    In polymer chemistry, ring-opening polymerization (ROP) is a form of chain-growth polymerization in which the terminus of a polymer chain attacks cyclic monomers to form a longer polymer (see figure). The reactive center can be radical, anionic or cationic. Ring-opening of cyclic monomers is often driven by the relief of bond-angle strain.

  9. C3H4O - Wikipedia

    en.wikipedia.org/wiki/C3H4O

    C 3 H 4 O is a chemical formula that represents each of several actual and hypothetical compounds that differ in structure, but each consist of three atoms of carbon, four of hydrogen, and one of oxygen. The following compounds are among them: