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  2. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    Since the S N 1 reaction involves formation of an unstable carbocation intermediate in the rate-determining step (RDS), anything that can facilitate this process will speed up the reaction. The normal solvents of choice are both polar (to stabilize ionic intermediates in general) and protic solvents (to solvate the leaving group in particular).

  3. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    Sigmatropic rearrangements are concisely described by an order term [i,j], which is defined as the migration of a σ-bond adjacent to one or more π systems to a new position (i−1) and (j−1) atoms removed from the original location of the σ-bond. [3]

  4. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    In the second step, the nucleophilic reagent (Nuc:) attaches to the carbocation and forms a covalent sigma bond. If the substrate has a chiral carbon, this mechanism can result in either inversion of the stereochemistry or retention of configuration. Usually, both occur without preference. The result is racemization.

  5. Bacterial recombination - Wikipedia

    en.wikipedia.org/wiki/Bacterial_recombination

    Bacterial recombination is a type of genetic recombination in bacteria characterized by DNA transfer from one organism called donor to another organism as recipient. This process occurs in three main ways: Transformation, the uptake of exogenous DNA from the surrounding environment. Transduction, the virus-mediated transfer of DNA between bacteria.

  6. Bacterial cellulose - Wikipedia

    en.wikipedia.org/wiki/Bacterial_cellulose

    The synthesis of bacterial cellulose is a multistep process that involve two main mechanisms: the synthesis of uridine diphosphoglucose (UDPGIc), followed by the polymerization of glucose into long and unbranched chains (the β-1→4 glucan chain) by cellulose synthase. Specifics on the cellulose synthesis has been extensively documented.

  7. 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.

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  9. Bacterial translation - Wikipedia

    en.wikipedia.org/wiki/Bacterial_translation

    Initiation of translation in bacteria involves the assembly of the components of the translation system, which are: the two ribosomal subunits (50S and 30S subunits); the mature mRNA to be translated; the tRNA charged with N-formylmethionine (the first amino acid in the nascent peptide); guanosine triphosphate (GTP) as a source of energy, and the three prokaryotic initiation factors IF1, IF2 ...

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