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  2. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    Formation of a tert-butyl carbocation by separation of a leaving group (a bromide anion) from the carbon atom: this step is slow. [5] Recombination of carbocation with nucleophile. Nucleophilic attack: the carbocation reacts with the nucleophile. If the nucleophile is a neutral molecule (i.e. a solvent) a third step is required to complete the ...

  3. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    A more detailed explanation of this can be found in the main SN1 reaction page. S N 2 reaction mechanism. The S N 2 mechanism has just one step. The attack of the reagent and the expulsion of the leaving group happen simultaneously. This mechanism always results in inversion of configuration.

  4. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    For example, the following hydrogen atom migration is of order [1,5], attained by counting counterclockwise through the π system, rather than the [1,3] order designation through the ring CH 2 group that would mistakenly result if counted clockwise. As a general approach, one can simply draw the transition state of the reaction.

  5. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    An example of a substitution reaction taking place by a so-called borderline mechanism as originally studied by Hughes and Ingold [6] is the reaction of 1-phenylethyl chloride with sodium methoxide in methanol. The reaction rate is found to the sum of S N 1 and S N 2 components with 61% (3,5 M, 70 °C) taking place by the latter.

  6. Walden inversion - Wikipedia

    en.wikipedia.org/wiki/Walden_inversion

    In the Walden inversion, the backside attack by the nucleophile in an S N 2 reaction gives rise to a product whose configuration is opposite to the reactant. Therefore, during S N 2 reaction, 100% inversion of product takes place. This is known as Walden inversion. It was first observed by chemist Paul Walden in 1896.

  7. Voltage-gated sodium channel - Wikipedia

    en.wikipedia.org/wiki/Voltage-gated_sodium_channel

    Voltage-gated sodium channels (VGSCs), also known as voltage-dependent sodium channels (VDSCs), are a group of voltage-gated ion channels found in the membrane of excitable cells (e.g., muscle, glial cells, neurons, etc.) with a permeability to the sodium ion Na +. They are the main channels involved in action potential of excitable cells.

  8. Sodium channel - Wikipedia

    en.wikipedia.org/wiki/Sodium_channel

    The protonation of these carboxylates is one of the main drivers of proton block in sodium channels, although there are other residues that also contribute to pH sensitivity. [53] One such residue is C373 in the cardiac sodium channel which makes it the most pH-sensitive sodium channel among the sodium channels that have been studied to date.

  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 ...