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  2. Neophyl chloride - Wikipedia

    en.wikipedia.org/wiki/Neophyl_chloride

    Neophyl chloride is a neopentyl halide which means it is subject to the neopentyl effect. This effect makes S N 2 nucleophilic substitution highly unlikely because of steric interactions due to the branching of the β-carbon. No rotamer of the molecule would allow a backside attack of the α carbon.

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...

  4. 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.

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    IUPAC Nomenclature ensures that each compound (and its various isomers) have only one formally accepted name known as the systematic IUPAC name. However, some compounds may have alternative names that are also accepted, known as the preferred IUPAC name which is generally taken from the common name of that compound. Preferably, the name should ...

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

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

    Names Preferred IUPAC name. 1-bromo-2,2 ... "Isomerization of Neopentyl Chloride and Neopentyl Bromide by a 1,2-Interchange of a Halogen Atom and a Methyl Group". ...

  7. 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.

  8. IUPAC nomenclature of inorganic chemistry 2005 - Wikipedia

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

    Apart from a reorganisation of the content, there is a new section on organometallics and a formal element list to be used in place of electronegativity lists in sequencing elements in formulae and names. The concept of a preferred IUPAC name (PIN), a part of the revised blue book for organic compound naming, has not yet been adopted for ...

  9. 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 ...