plural of di-pimethane rearrangement

(chemistry) any of many classes of reaction in which an atom or bond moves or migrates from a site in a reactant molecule to a different site in a product molecule

plural of rearrangement reaction

(organic chemistry) A rearrangement involving a carbocation with a hydroxy group adjacent to the electron-deficient centre.

(organic chemistry) A class of rearrangement reaction in which a 1,2-diol is converted into a ketone; especially the case of the conversion of pinacol into pinacolone

(organic chemistry) A reaction in which an α-diazocarbonyl compound is converted into a ketene and then into a variety of other compounds

(organic chemistry) Synonym of Schmidt reaction

(organic chemistry) The (normally reversible) thermal isomerization of a 1,5-diene to yield a more stable regioisomer

(organic chemistry) A powerful carbon–carbon bond-forming chemical reaction, in which the heating of an allyl vinyl ether initiates a [3,3]-sigmatropic rearrangement to give a γ,δ-unsaturated carbonyl.

(organic chemistry) A rearrangement name reaction in which an organosilyl group switches position with a hydroxyl proton over a carbon-to-oxygen covalent bond under the influence of a base, yielding a silyl ether.