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Regioselectivity

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In organic chemistry, regioselectivity is the preference of chemical bonding or breaking in one direction over all other possible directions.[1][2] It can often apply to which of many possible positions a reagent will affect, such as which proton a strong base will abstract from an organic molecule, or where on a substituted benzene ring a further substituent will be added.

A specific example is a halohydrin formation reaction with 2-propenylbenzene:[3]

Regioselectivity in halohydrin formation

Because of the preference for the formation of one product over another, the reaction is selective. This reaction is regioselective because it selectively generates one constitutional isomer rather than the other.

Various examples of regioselectivity have been formulated as rules for certain classes of compounds under certain conditions, many of which are named. Among the first introduced to chemistry students are Markovnikov's rule for the addition of protic acids to alkenes, and the Fürst-Plattner rule for the addition of nucleophiles to derivatives of cyclohexene, especially epoxide derivatives.[4][5]

Regioselectivity in ring-closure reactions is subject to Baldwin's rules. If there are two or more orientations that can be generated during a reaction, one of them is dominant (e.g., Markovnikov/anti-Markovnikov addition across a double bond)

Regioselectivity can also be applied to specific reactions such as addition to pi ligands.

Selectivity also occurs in carbene insertions, for example in the Baeyer-Villiger reaction. In this reaction, an oxygen is regioselectively inserted near an adjacent carbonyl group. In ketones, this insertion is directed toward the carbon which is more highly substituted (i.e. according to Markovnikov's rule). For example, in a study involving acetophenones, this oxygen was preferentially inserted between the carbonyl and the aromatic ring to give acetyl aromatic esters instead of methyl benzoates.[6]

See also

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References

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  1. ^ March, Jerry (1985). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (3rd ed.). New York: Wiley. ISBN 9780471854722. OCLC 642506595.
  2. ^ http://www.chem.ucalgary.ca/courses/351/Carey5th/Ch06/ch6-0-1.html Regioselectivity & Stereoselectivity
  3. ^ Regioselectivity in Organic Synthesis: Preparation of the Bromohydrin of alpha-Methylstyrene Brad Andersh, Kathryn N. Kilby, Meghan E. Turnis, and Drew L. Murphy 102 Journal of Chemical Education • Vol. 85 No. 1 January 2008
  4. ^ W. Markownikoff (1870). "Ueber die Abhängigkeit der verschiedenen Vertretbarkeit des Radicalwasserstoffs in den isomeren Buttersäuren". Annalen der Pharmacie 153 (1): 228–259.
  5. ^ Fürst, A.; Plattner, P. A. Helv. Chim. Acta 1949, 32, 275
  6. ^ Palmer, Billy W.; Fry, Arthur (1970). "Variation of carbon-14 isotope effect with substituent and the mechanism of the m-chloroperbenzoic acid oxidation of laeled para-substituted acetophenones". Journal of the American Chemical Society. 92 (8): 2580–2581. doi:10.1021/ja00711a079.