molecular rearrangement

Preferred Label : molecular rearrangement;

IUPAC definition : 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: The definition of molecular rearrangement includes changes in which there is a bond migration of an atom or bond (unexpected on the basis of the principle of minimum structural change), as in the reaction: where the rearrangement stage can formally be represented as the '1,2-shift' of hydride between adjacent carbon atoms in the carbocation: Such migrations occur also in radicals, e.g.: 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': 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:;

Details

Origin ID

M03997;

See also
- bond migration [IUPAC Term]
- carbocation [IUPAC Term]
- chemical species [IUPAC Term]
- connectivity [IUPAC Term]
- degenerate rearrangement [IUPAC Term]
- electrocyclic reaction [IUPAC Term]
- entering group [IUPAC Term]
- functional group [IUPAC Term]
- hydride [IUPAC Term]
- hydron [IUPAC Term]
- intermolecular [IUPAC Term]
- intramolecular [IUPAC Term]
- isomeric [IUPAC Term]
- isomerization [IUPAC Term]
- leaving group [IUPAC Term]
- migration [IUPAC Term]
- oxidation [IUPAC Term]
- principle of minimum structural change [IUPAC Term]
- pseudomolecular rearrangement [IUPAC Term]
- rearrangement [IUPAC Term]
- rearrangement stage [IUPAC Term]
- sigmatropic rearrangement [IUPAC Term]
- substitution reaction [IUPAC Term]
- tautomerization [IUPAC Term]
- transformation [IUPAC Term]

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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: The definition of molecular rearrangement includes changes in which there is a bond migration of an atom or bond (unexpected on the basis of the principle of minimum structural change), as in the reaction: where the rearrangement stage can formally be represented as the '1,2-shift' of hydride between adjacent carbon atoms in the carbocation: Such migrations occur also in radicals, e.g.: 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': 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: