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molecular rearrangement

Also contains definition of: principle of minimum structural change

The term is traditionally applied to any reaction that involves a change of connectivity (sometimes including hydrogen), and violates the so-called 'principle of minimum structural change'. According to this oversimplified principle, chemical species do not isomerize in the course of a transformation, e.g. substitution, or the change of a functional group of a chemical species into a different functional group is not expected to involve the making or breaking of more than the minimum number of bonds required to effect that transformation. For example, any new substituents are expected to enter the precise positions previously occupied by displaced groups. The simplest type of rearrangement is an intramolecular reaction in which the product is isomeric with the reactant (one type of 'intramolecular isomerization'). An example is the first step of the Claisen rearrangement:
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The definition of molecular rearrangement includes changes in which there is a migration of an atom or bond (unexpected on the basis of the principle of minimum structural change), as in the reaction:
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where the rearrangement stage can formally be represented as the '1,2-shift' of hydride between adjacent carbon atoms in the carbocation:
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Such migrations occur also in radicals, e.g.:
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The definition also includes reactions in which an entering group takes up a different position from the leaving group, with accompanying bond migration. An example of the latter type is the 'allylic rearrangement':
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A distinction is made between 'intramolecular rearrangements' (or 'true molecular rearrangements') and ' intermolecular rearrangements' (or 'apparent rearrangements'). In the former case the atoms and groups that are common to a reactant and a product never separate into independent fragments during the rearrangement stage (i.e. the change is intramolecular), whereas in an 'intermolecular rearrangement' a migrating group is completely free from the parent molecule and is re-attached to a different position in a subsequent step, as in the Orton reaction:
M03997-6
Source:
PAC, 1994, 66, 1077 (Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)) on page 1142
InChI=1/C9H10O/c1-2-8-10-9-6-4-3-5-7-9/h2-7H,1,8H2
POSICDHOUBKJKP-UHFFFAOYAP
InChI=1/C9H10O/c1-2-5-8-6-3-4-7-9(8)10/h2-4,6-8H,1,5H2
SMCGDSTZXIBJCB-UHFFFAOYAQ
InChI=1/C9H10O/c1-2-5-8-6-3-4-7-9(8)10/h2-4,6-7,10H,1,5H2
QIRNGVVZBINFMX-UHFFFAOYAY
InChI=1/C5H9Br/c1-5(2)3-4-6/h3H,4H2,1-2H3
LOYZVRIHVZEDMW-UHFFFAOYAP
InChI=1/H2O/h1H2/p-1/fHO/h1h/q-1
XLYOFNOQVPJJNP-GDBKARAACO
InChI=1/C5H10O/c1-4-5(2,3)6/h4,6H,1H2,2-3H3
HNVRRHSXBLFLIG-UHFFFAOYAW
InChI=1/BrH/h1H/p-1/fBr/h1h/q-1
CPELXLSAUQHCOX-ZMJNGJBWCE
InChI=1/C8H8ClNO/c1-7(11)10(9)8-5-3-2-4-6-8/h2-6H,1H3
QNVKMXGRFVLMBM-UHFFFAOYAF
InChI=1/ClH/h1H
VEXZGXHMUGYJMC-UHFFFAOYAT
InChI=1/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)/f/h9H
FZERHIULMFGESH-BGGKNDAXCW
InChI=1/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)/f/h9H
FZERHIULMFGESH-BGGKNDAXCW
InChI=1/CH3Cl/c1-2/h1H3
NEHMKBQYUWJMIP-UHFFFAOYAW
InChI=1/ClH/h1H
VEXZGXHMUGYJMC-UHFFFAOYAT
InChI=1/C3H7Br/c1-2-3-4/h2-3H2,1H3
CYNYIHKIEHGYOZ-UHFFFAOYAN
InChI=1/Ag.BrH/h;1H/q+1;/p-1/fAg.Br/h;1h/qm;-1
ADZWSOLPGZMUMY-FTLIPQIBCJ
InChI=1/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1/fC2H3O2.Ag/q-1;m
CQLFBEKRDQMJLZ-HNVJNUBOCV
InChI=1/C5H10O2/c1-4(2)7-5(3)6/h4H,1-3H3
JMMWKPVZQRWMSS-UHFFFAOYAA
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: doi:10.1351/goldbook.M03997.
Original PDF version: http://www.iupac.org/goldbook/M03997.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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