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  2. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    All feature three contiguous sp²-hybridized carbon centers and all derive stability from resonance. [6] Each species can be presented by two resonance structures with the charge or unpaired electron distributed at both 1,3 positions. Resonance structure of the allyl anion. The cation is identical, but carries an opposite-sign charge. [7]

  3. Transmetalation - Wikipedia

    en.wikipedia.org/wiki/Transmetalation

    In redox-transmetalation/ligand exchange the ligands of two metal complexes switch places with each other, bonding with the other metal center. The R ligand can be an alkyl, aryl, alkynyl, or allyl group and the X ligand can be a halogen, pseudo-halogen, alkyl, or aryl group. The reaction can proceed by two possible intermediate steps.

  4. Baeyer–Villiger oxidation - Wikipedia

    en.wikipedia.org/wiki/Baeyer–Villiger_oxidation

    The migratory ability is ranked tertiary > secondary > aryl > primary. [7] Allylic groups are more apt to migrate than primary alkyl groups but less so than secondary alkyl groups. [5] Electron-withdrawing groups on the substituent decrease the rate of migration. [8] There are two explanations for this trend in migration ability. [9]

  5. β-Carbon elimination - Wikipedia

    en.wikipedia.org/wiki/Β-Carbon_elimination

    β-Carbon elimination (beta-carbon elimination) is a type of reaction in organometallic chemistry wherein an allyl ligand bonded to a metal center is broken into the corresponding metal-bonded alkyl (aryl) ligand and an alkene. [1] It is a subgroup of elimination reactions.

  6. β-Hydride elimination - Wikipedia

    en.wikipedia.org/wiki/Β-Hydride_elimination

    β-Hydride elimination is a reaction in which a metal-alkyl centre is converted into the corresponding metal-hydride-alkene. [1] β-Hydride elimination can also occur for many alkoxide complexes as well. The main requirements are that the alkyl group possess a C-H bond β to the metal and that the metal be coordinatively unsaturated.

  7. Metal–halogen exchange - Wikipedia

    en.wikipedia.org/wiki/Metal–halogen_exchange

    Lithium–halogen exchange is frequently used to prepare vinyl-, aryl- and primary alkyllithium reagents. Vinyl halides usually undergo lithium–halogen exchange with retention of the stereochemistry of the double bond. [2] The presence of alkoxyl or related chelating groups accelerates lithium–halogen exchange. [3]

  8. Finkelstein reaction - Wikipedia

    en.wikipedia.org/wiki/Finkelstein_reaction

    Vinyl, aryl and tertiary alkyl halides are unreactive; as a result, the reaction of NaI in acetone can be used as a qualitative test to determine which of the aforementioned classes an unknown alkyl halide belongs to, with the exception of alkyl iodides, as they yield the same product upon substitution.

  9. Aryl group - Wikipedia

    en.wikipedia.org/wiki/Aryl_group

    A phenyl group is the simplest aryl group, here bonded to an "R" group. In organic chemistry, an aryl is any functional group or substituent derived from an aromatic ring, usually an aromatic hydrocarbon, such as phenyl and naphthyl. [1] "Aryl" is used for the sake of abbreviation or generalization, and "Ar" is used as a placeholder for the ...