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  2. Carbocation - Wikipedia

    en.wikipedia.org/wiki/Carbocation

    Carbocations were also found to be involved in the S N 1 reaction, the E1 reaction, and in rearrangement reactions such as the Whitmore 1,2 shift. The chemical establishment was reluctant to accept the notion of a carbocation and for a long time the Journal of the American Chemical Society refused articles that mentioned them.

  3. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    Hammond's postulate is useful for understanding the relationship between the rate of a reaction and the stability of the products. While the rate of a reaction depends just on the activation energy (often represented in organic chemistry as ΔG ‡ “delta G double dagger”), the final ratios of products in chemical equilibrium depends only ...

  4. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    The carbocation intermediate formed in the reaction's rate determining step (RDS) is an sp 2 hybridized carbon with trigonal planar molecular geometry. This allows two different ways for the nucleophilic attack, one on either side of the planar molecule.

  5. Pinacol rearrangement - Wikipedia

    en.wikipedia.org/wiki/Pinacol_rearrangement

    The reaction product he obtained instead he called paraceton which he believed to be an acetone dimer. In his second publication in 1860 he reacted paraceton with sulfuric acid (the actual pinacol rearrangement). Again Fittig was unable to assign a molecular structure to the reaction product which he assumed to be another isomer or a polymer.

  6. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    If the substrate that is undergoing S N 2 reaction has a chiral centre, then inversion of configuration (stereochemistry and optical activity) may occur; this is called the Walden inversion. For example, 1-bromo-1-fluoroethane can undergo nucleophilic attack to form 1-fluoroethan-1-ol, with the nucleophile being an HO − group. In this case ...

  7. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    In organic chemistry, a rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule. [1] Often a substituent moves from one atom to another atom in the same molecule, hence these reactions are usually intramolecular.

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  9. Damköhler numbers - Wikipedia

    en.wikipedia.org/wiki/Damköhler_numbers

    Since the reaction rate determines the reaction timescale, the exact formula for the Damköhler number varies according to the rate law equation. For a general chemical reaction A → B following the Power law kinetics of n-th order , the Damköhler number for a convective flow system is defined as: