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  2. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    A generic 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. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Alternatively, an ether chain can be named as an alkane in which one carbon is replaced by an oxygen, a replacement denoted by the prefix "oxa". For example, CH 3 OCH 2 CH 3 could also be called 2-oxabutane, and an epoxide could be called oxacyclopropane.

  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. Nomenclature of Organic Chemistry - Wikipedia

    en.wikipedia.org/wiki/Nomenclature_of_Organic...

    Nomenclature of Organic Chemistry, commonly referred to by chemists as the Blue Book, is a collection of recommendations on organic chemical nomenclature published at irregular intervals by the International Union of Pure and Applied Chemistry (IUPAC).

  6. Geneva Rules - Wikipedia

    en.wikipedia.org/wiki/Geneva_Rules

    The Geneva rules for nomenclature were described in 62 paragraphs. [2] Some of these rules were: Saturated hydrocarbons would have names ending in -ane. The traditional names of the first 4 in the series was to be kept (methane, ethane, propane and butane)

  7. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    Heterocyclic organic compounds can be usefully classified based on their electronic structure. The saturated organic heterocycles behave like the acyclic derivatives. Thus, piperidine and tetrahydrofuran are conventional amines and ethers, with modified steric profiles. Therefore, the study of organic heterocyclic chemistry focuses on organic ...

  8. Category:Epoxides - Wikipedia

    en.wikipedia.org/wiki/Category:Epoxides

    An epoxide is a cyclic ether with three ring atoms. ... Pages in category "Epoxides" The following 154 pages are in this category, out of 154 total.

  9. Preferred IUPAC name - Wikipedia

    en.wikipedia.org/wiki/Preferred_IUPAC_name

    In chemical nomenclature, a preferred IUPAC name (PIN) is a unique name, assigned to a chemical substance and preferred among all possible names generated by IUPAC nomenclature. The "preferred IUPAC nomenclature" provides a set of rules for choosing between multiple possibilities in situations where it is important to decide on a unique name.