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  2. IUPAC nomenclature of organic chemistry - Wikipedia

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

    Ethers (R−O−R) consist of an oxygen atom between the two attached carbon chains. The shorter of the two chains becomes the first part of the name with the -ane suffix changed to -oxy, and the longer alkane chain becomes the suffix of the name of the ether.

  3. 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 ...

  4. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    In chemistry, a phenol ether (or aromatic ether) is an organic compound derived from phenol (C 6 H 5 OH), where the hydroxyl (-OH) group is substituted with an alkoxy (-OR) group. Usually phenol ethers are synthesized through the condensation of phenol and an organic alcohol ; however, other known reactions regarding the synthesis of ethers can ...

  5. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    Polymer nomenclature usually applies to idealized representations meaning minor structural irregularities are ignored. A polymer can be named in one of two ways. Source-based nomenclature can be used when the monomer can be identified. Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven.

  6. Alkoxy group - Wikipedia

    en.wikipedia.org/wiki/Alkoxy_group

    An ethoxy group (CH 3 CH 2 O−) is found in the organic compound ethyl phenyl ether (C 6 H 5 OCH 2 CH 3, also known as ethoxybenzene). Related to alkoxy groups are aryloxy groups, which have an aryl group singularly bonded to oxygen such as the phenoxy group (C 6 H 5 O−). An alkoxy or aryloxy group bonded to an alkyl or aryl (R−O−R') is ...

  7. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    Some sulfides are named by modifying the common name for the corresponding ether. For example, C 6 H 5 SCH 3 is methyl phenyl sulfide, but is more commonly called thioanisole, since its structure is related to that for anisole, C 6 H 5 OCH 3. The modern systematic nomenclature in chemistry for the trival name thioether is sulfane. [2]

  8. Category:Ethers - Wikipedia

    en.wikipedia.org/wiki/Category:Ethers

    Pages in category "Ethers" The following 200 pages are in this category, out of approximately 329 total. This list may not reflect recent changes.

  9. Crown ether - Wikipedia

    en.wikipedia.org/wiki/Crown_ether

    The first number in a crown ether's name refers to the number of atoms in the cycle, and the second number refers to the number of those atoms that are oxygen. Crown ethers are much broader than the oligomers of ethylene oxide; an important group are derived from catechol. Crown ethers strongly bind certain cations, forming complexes. The ...