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  2. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    When the solvent is also a nucleophile such as dioxane two successive S N 2 reactions take place and the stereochemistry is again retention. With standard S N 1 reaction conditions the reaction outcome is retention via a competing S N i mechanism and not racemization and with pyridine added the result is again inversion. [5] [3]

  3. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    The Hughes-Ingold symbol of the mechanism expresses two properties—"S N" stands for "nucleophilic substitution", and the "1" says that the rate-determining step is unimolecular. [1] [2] Thus, the rate equation is often shown as having first-order dependence on the substrate and zero-order dependence on the nucleophile. This relationship holds ...

  4. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    The two reactions are named according tho their rate law, with S N 1 having a first-order rate law, and S N 2 having a second-order. [2] S N 1 reaction mechanism occurring through two steps. The S N 1 mechanism has two steps. In the first step, the leaving group departs, forming a carbocation (C +). In the second step, the nucleophilic reagent ...

  5. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    As a general approach, one can simply draw the transition state of the reaction. For a sigmatropic reaction, the transition state will consist of two fragments, joined by the forming and breaking σ-bonds. The sigmatropic reaction is named as a [i,j]-sigmatropic rearrangement (i ≤ j) if these two fragments consist of i and j atoms. This is ...

  6. Walden inversion - Wikipedia

    en.wikipedia.org/wiki/Walden_inversion

    Walden inversion is the inversion of a stereogenic center in a chiral molecule in a chemical reaction. Since a molecule can form two enantiomers around a stereogenic center, the Walden inversion converts the configuration of the molecule from one enantiomeric form to the other.

  7. Protein splicing - Wikipedia

    en.wikipedia.org/wiki/Protein_splicing

    The process for class 1 inteins begins with an N-O or N-S shift when the side chain of the first residue (a serine, threonine, or cysteine) of the intein portion of the precursor protein nucleophilically attacks the peptide bond of the residue immediately upstream (that is, the final residue of the N-extein) to form a linear ester (or thioester) intermediate.

  8. Cell fusion - Wikipedia

    en.wikipedia.org/wiki/Cell_fusion

    Cell fusion is an important cellular process in which several uninucleate cells (cells with a single nucleus) combine to form a multinucleate cell, known as a syncytium. Cell fusion occurs during differentiation of myoblasts , osteoclasts and trophoblasts , during embryogenesis , and morphogenesis . [ 1 ]

  9. Gating (electrophysiology) - Wikipedia

    en.wikipedia.org/wiki/Gating_(electrophysiology)

    A variety of cellular changes can trigger gating, depending on the ion channel, including changes in voltage across the cell membrane (voltage-gated ion channels), chemicals interacting with the ion channel (ligand-gated ion channels), changes in temperature, [4] stretching or deformation of the cell membrane, addition of a phosphate group to ...

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