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  2. Neopentyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_alcohol

    Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. [3] It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride . Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with ...

  3. Neophyl chloride - Wikipedia

    en.wikipedia.org/wiki/Neophyl_chloride

    C 6 H 5 C(CH 3) 2 CH 2 OH + SOCl 2 → C 6 H 5 C(CH 3) 2 CH 2 Cl + HCl + SO 2. It is easily prepared on a large scale from benzene and methallyl chloride by an electrophilic aromatic substitution reaction, using sulfuric acid as the catalyst: [4] The reaction is an example of an electrophilic aromatic substitution reaction. H 2 C=C(CH 3)CH 2 Cl ...

  4. IUPAC nomenclature of chemistry - Wikipedia

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

    The main structure of chemical names according to IUPAC nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry (Red Book) IUPAC nomenclature of organic chemistry (Blue Book)

  5. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).

  6. 1-Bromo-2,2-dimethylpropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-2,2-dimethylpropane

    Preferred IUPAC name. 1-bromo-2,2-dimethylpropane [1] Other names ... "Isomerization of Neopentyl Chloride and Neopentyl Bromide by a 1,2-Interchange of a Halogen ...

  7. 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

  8. 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.

  9. Neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol...

    Neopentyl glycol diglycidyl ether (NPGDGE) is an organic chemical in the glycidyl ether family. It is aliphatic and a colorless liquid. It has the formula C 11 H 20 O 4 and the CAS registry number of 17557-23-2. [2] It has two oxirane groups per molecule. [3] Its principle use is in modifying epoxy resins. [4] It is REACH registered. [5]