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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. Vinyl cation - Wikipedia

    en.wikipedia.org/wiki/Vinyl_cation

    Vinyl cations were first proposed in 1944 as a reactive intermediate for the acid-catalyzed hydrolysis of alkoxyacetylenes to give alkyl acetate. [5] In the first step of their facile hydration reaction, which was the rate limiting step, a vinyl cation reactive intermediate was proposed; the positive charge was believed to formally lie on a ...

  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. 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]

  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. Michaelis–Arbuzov reaction - Wikipedia

    en.wikipedia.org/wiki/Michaelis–Arbuzov_reaction

    In general, tertiary alkyl halides, aryl halides and vinyl halides do not react. There are notable exceptions to this trend, including 1,2-dichloroethene and trityl halides. Some activated aryl halides, often involving heterocycles have been known to undergo the reaction.

  9. 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.