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  2. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    Many reactions studied are solvolysis reactions where a solvent molecule (often an alcohol) is the nucleophile. While still a second order reaction mechanistically, the reaction is kinetically first order as the concentration of the nucleophile–the solvent molecule, is effectively constant during the reaction.

  3. Associative substitution - Wikipedia

    en.wikipedia.org/wiki/Associative_substitution

    Associative substitution describes a pathway by which compounds interchange ligands. The terminology is typically applied to organometallic and coordination complexes, but resembles the Sn2 mechanism in organic chemistry. The opposite pathway is dissociative substitution, being analogous to the Sn1 pathway. Intermediate pathways exist between ...

  4. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The two main mechanisms were the S N 1 reaction and the S N 2 reaction, where S stands for substitution, N stands for nucleophilic, and the number represents the kinetic order of the reaction. [4] In the S N 2 reaction, the addition of the nucleophile and the elimination of leaving group take place simultaneously (i.e. a concerted reaction).

  5. Concerted reaction - Wikipedia

    en.wikipedia.org/wiki/Concerted_reaction

    The rate of the S N 2 reaction is second order overall due to the reaction being bimolecular (i.e. there are two molecular species involved in the rate-determining step). The reaction does not have any intermediate steps, only a transition state. This means that all the bond making and bond breaking takes place in a single step. In order for ...

  6. Walden inversion - Wikipedia

    en.wikipedia.org/wiki/Walden_inversion

    In this reaction, the silver oxide in the first step acts as a hydroxide donor while the silver ion plays no role in the reaction. The intermediates are the carboxyl dianion A which gives an intramolecular nucleophilic substitution by the β-carboxylate anion to produce a four-membered β- lactone ring B .

  7. 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 ...

  8. Marjorie Taylor Greene to work with Musk's new government ...

    www.aol.com/news/marjorie-taylor-greene-musks...

    Republican Marjorie Taylor Greene said on Thursday she will chair a U.S. House of Representatives panel on government efficiency, working with billionaire Elon Musk and Vivek Ramaswamy in their ...

  9. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    Factors that affect the rate determining step are stereochemistry, leaving groups, and base strength. A theory, for an E2 reaction, by Joseph Bunnett suggests the lowest pass through the energy barrier between reactants and products is gained by an adjustment between the degrees of C β -H and C α -X rupture at the transition state.