enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Neopentane - Wikipedia

    en.wikipedia.org/wiki/Neopentane

    The preferred IUPAC name is the systematic name 2,2-dimethylpropane, but the substituent numbers are superfluous because it is the only possible “dimethylpropane”. A neopentyl group attached to a generic group R. A neopentyl substituent, often symbolized by "Np", has the structure Me 3 C–CH 2 – for instance neopentyl alcohol (Me 3 CCH 2 OH

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    For secondary amines (of the form R−NH−R), the longest carbon chain attached to the nitrogen atom becomes the primary name of the amine; the other chain is prefixed as an alkyl group with location prefix given as an italic N: CH 3 NHCH 2 CH 3 is N-methylethanamine.

  4. Glycan nomenclature - Wikipedia

    en.wikipedia.org/wiki/Glycan_nomenclature

    Glycan nomenclature is the systematic naming of glycans, which are carbohydrate-based polymers made by all living organisms. In general glycans can be represented in (i) text formats, these include commonly used CarbBank, IUPAC name, and several other types; and (ii) symbol formats, these are consisting of Symbol Nomenclature For Glycans and Oxford Notations.

  5. IUPAC nomenclature of chemistry - Wikipedia

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

    IUPAC nomenclature is used for the naming of chemical compounds, based on their chemical composition and their structure. [1] For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain.

  6. Neopentyl glycol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol

    Neopentyl glycol (IUPAC name: 2,2-dimethylpropane-1,3-diol) is an organic chemical compound. It is used in the synthesis of polyesters , paints , lubricants , and plasticizers . When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water.

  7. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    In its open-chain form, the glucose molecule has an open (as opposed to cyclic) unbranched backbone of six carbon atoms, where C-1 is part of an aldehyde group H(C=O)−. Therefore, glucose is also classified as an aldose, or an aldohexose. The aldehyde group makes glucose a reducing sugar giving a positive reaction with the Fehling test.

  8. International Union of Pure and Applied Chemistry - Wikipedia

    en.wikipedia.org/wiki/International_Union_of...

    IUPAC organic nomenclature has three basic parts: the substituents, carbon chain length, and chemical affix. [13] The substituents are any functional groups attached to the main carbon chain. The main carbon chain is the longest possible continuous chain. The chemical affix denotes what type of molecule it is.

  9. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The numbers are included in the name to avoid ambiguity about the position of the groups, and "tri" indicates that there are three identical methyl groups. If one of the methyl groups attached to the third carbon atom were instead an ethyl group, then the name would be 3-ethyl-2,3-dimethylpentane.