Abstract
Standard nomenclature is well known, but it may be noted that (a) iso- (to denote terminal CHMe2) is restricted to C3–C6, t- (tertiary) to C4 and C5, and s- (secondary) to C4*, (b) such modified names may never be used for substituted derivatives of the compounds or radicals, e.g., CHMe2·CHCl- is 1-chloro-2-methylpropyl, and (c) the free valency of radicals always has number 1, e.g., Prn 2CH- is 1-propylbutyl and not 4-heptyl.
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References
IUPAG Nomenclature of Organic Chemistry, 1957, Sections A and B. Butterworths, London, 2nd edn., 1966.
IUPAG Nomenclature of Organic Chemistry, 1965, Section G. Butterworths, London, 1965.
Stelzneb, R., Literatur-Register der organischen Chemie, Springer, Berlin, 1931, Vol. III, 1914–15, pp. 22–24.
von Bayer, A., Ber. dtsch. chem. Ges., 1900, 33, 3771; alse ref. 1.
Hantzsch, A. and Weber, J. H., Ber. dtsch. chem. Ges., 1887, 20, 3119;
Widman, O., J.prakt. Chem., 1888, [2], 38, 185; also ref. 1.
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Cahn, R.S. (1968). Organic: Skeletal Types. In: An Introduction to Chemical Nomenclature. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-6598-1_7
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DOI: https://doi.org/10.1007/978-1-4899-6598-1_7
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