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  2. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    A singlet carbene contains an empty p orbital and a roughly sp 2 hybrid orbital that has two electrons. Singlet carbenes add stereospecifically to alkenes, and alkene stereochemistry is retained in the cyclopropane product. [1] The mechanism for addition of a carbene to an alkene is a concerted [2+1] cycloaddition (see figure).

  3. Carbene - Wikipedia

    en.wikipedia.org/wiki/Carbene

    Carbene radicals, in which the carbene is bonded to an open-shell metal with the carbene carbon possessing a radical character. Carbene radicals have features of both Fischer and Schrock carbenes, but are typically long-lived reaction intermediates. The "second generation" of the Grubbs catalysts for alkene metathesis features an NHC ligand.

  4. Carbene dimerization - Wikipedia

    en.wikipedia.org/wiki/Carbene_dimerization

    In this reaction type either the two carbenic intermediates react or a carbenic intermediate reacts with a carbene precursor. [1] An early pioneer was Christoph Grundmann reporting on a carbene dimerisation in 1938. [2] In the domain of persistent carbenes the Wanzlick equilibrium describes an equilibrium between a carbene and its alkene.

  5. Transition metal carbene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carbene...

    A transition metal carbene complex is an organometallic compound featuring a divalent carbon ligand, itself also called a carbene. [1] Carbene complexes have been synthesized from most transition metals and f-block metals , [ 2 ] using many different synthetic routes such as nucleophilic addition and alpha-hydrogen abstraction. [ 1 ]

  6. Cationic polymerization - Wikipedia

    en.wikipedia.org/wiki/Cationic_polymerization

    Propagation proceeds by addition of monomer to the active species, i.e. the carbenium ion. The monomer is added to the growing chain in a head-to-tail fashion; in the process, the cationic end group is regenerated to allow for the next round of monomer addition. [6] General propagation pathway

  7. Carbene radical - Wikipedia

    en.wikipedia.org/wiki/Carbene_radical

    Bonding scheme of carbene radical complexes as compared to Schrock and Fischer-type carbene complexes. Carbene radicals are a special class of organometallic carbenes.The carbene radical can be formed by one-electron reduction of Fischer-type carbenes using an external reducing agent, or directly upon carbene formation at an open-shell transition metal complex (in particular low-spin cobalt(II ...

  8. How to watch the ‘Rudolph the Red-Nosed Reindeer’ NBC ...

    www.aol.com/entertainment/rudolph-red-nosed...

    You can stream Rudolph and Frosty's Christmas In July on AMC+ (or via the AMC+ Amazon Prime Video add-on, which offers a free trial). Watch on Amazon Prime Video More ways to watch NBC live ...

  9. Addition reaction - Wikipedia

    en.wikipedia.org/wiki/Addition_reaction

    In organic chemistry, an addition reaction is an organic reaction in which two or more molecules combine to form a larger molecule called the adduct. [ 1 ] [ 2 ] An addition reaction is limited to chemical compounds that have multiple bonds .