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・ 1,2-dihydroxynaphthalene dioxygenase
・ 1,2-Diiodoethane
・ 1,2-Dimethoxybenzene
・ 1,2-Dimethylcyclopropane
・ 1,2-Dimethylhydrazine
・ 1,2-dioleoyl-sn-glycerophosphoethanolamine
・ 1,2-Dioxane
・ 1,2-Dioxetane
・ 1,2-Dioxetanedione
・ 1,2-Dioxin
・ 1,2-Dithietane
・ 1,2-Dithiole
・ 1,2-Ethanedithiol
・ 1,2-Naphthoquinone
・ 1,2-Propanedithiol
1,2-rearrangement
・ 1,2-Wittig rearrangement
・ 1,227 QI Facts to Blow Your Socks Off
・ 1,3,2,4-Dithiadiphosphetane 2,4-disulfides
・ 1,3,3,3-Tetrafluoropropene
・ 1,3,5-Triazido-2,4,6-trinitrobenzene
・ 1,3,5-Triazine
・ 1,3,5-Trichlorobenzene
・ 1,3,5-Trinitrobenzene
・ 1,3,5-Trioxane
・ 1,3,5-Trioxanetrione
・ 1,3,5-Trithiane
・ 1,3,6-Trigalloyl glucose
・ 1,3,7-Trimethyluric acid
・ 1,3,8-Trihydroxyanthraquinone


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1,2-rearrangement : ウィキペディア英語版
1,2-rearrangement
A 1,2-rearrangement or 1,2-migration or 1,2-shift or Whitmore 1,2-shift is an organic reaction where a substituent moves from one atom to another atom in a chemical compound. In a 1,2 shift the movement involves two adjacent atoms but moves over larger distances are possible. In the example below the substituent R moves from carbon atom C2 to C3.

The rearrangement is intramolecular and the starting compound and reaction product are structural isomers. The 1,2-rearrangement belongs to a broad class of chemical reactions called rearrangement reactions.
A rearrangement involving a hydrogen atom is called a 1,2-hydride shift. If the substituent being rearranged is an alkyl group, it is named according to the alkyl group's anion: i.e. 1,2-methanide shift, 1,2-ethanide shift, etc.
== Reaction mechanism ==
A 1,2-rearrangement is often initialised by the formation of a reactive intermediate such as:
*a carbocation by heterolysis in a nucleophilic rearrangement or anionotropic rearrangement
*a carbanion in a electrophilic rearrangement or cationotropic rearrangement
*a free radical by homolysis
*a nitrene.
The driving force for the actual migration of a substituent in step two of the rearrangement is the formation of a more stable intermediate. For instance a tertiary carbocation is more stable than a secondary carbocation and therefore the SN1 reaction of neopentyl bromide with ethanol yields tert-pentyl ethyl ether.

Carbocation rearrangements are more common than the carbanion or radical counterparts. This observation can be explained on the basis of Hückel's rule. A cyclic carbocationic transition state is aromatic and stabilized because it holds 2 electrons. In an anionic transition state on the other hand 4 electrons are present thus antiaromatic and destabilized. A radical transition state is neither stabilized or destabilized.
The most important carbocation 1,2-shift is the Wagner–Meerwein rearrangement. A carbanionic 1,2-shift is involved in the benzilic acid rearrangement.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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