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  2. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    The E2 mechanism, where E2 stands for bimolecular elimination, involves a one-step mechanism in which carbon-hydrogen and carbon-halogen bonds break to form a double bond (C=C Pi bond). The specifics of the reaction are as follows: E2 is a single step elimination, with a single transition state.

  3. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    There are two types of elimination reactions, E1 and E2. An E2 reaction is a One step mechanism in which carbon-hydrogen and carbon-halogen bonds break to form a double bond. C=C Pi bond. An E1 reaction is the Ionization of the carbon-halogen bond breaking to give a carbocation intermediate, then the Deprotonation of the carbocation.

  4. E1cB-elimination reaction - Wikipedia

    en.wikipedia.org/wiki/E1cB-elimination_reaction

    The E1cB mechanism is just one of three types of elimination reaction. The other two elimination reactions are E1 and E2 reactions. Although the mechanisms are similar, they vary in the timing of the deprotonation of the α-carbon and the loss of the leaving group. E1 stands for unimolecular elimination, and E2 stands for bimolecular elimination.

  5. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    In an E2 mechanism, a base takes a proton near the leaving group, forcing the electrons down to make a double bond, and forcing off the leaving group-all in one concerted step. The rate law depends on the first order concentration of two reactants, making it a 2nd order (bimolecular) elimination reaction.

  6. Estradiol - Wikipedia

    en.wikipedia.org/wiki/Estradiol

    Estradiol (E2), also called oestrogen, oestradiol, ... which is the predominant mechanism by which estradiol mediates its biological effects in the body.

  7. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    The mechanism for the Hofmann elimination is generally E2, but can go through an E i pathway under certain circumstances. For some sterically hindered molecules the base deprotonates a methyl group on the amine instead of the β-hydrogen directly, forming an ylide intermediate which eliminates trimethylamine through a 5-membered transition ...

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    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  9. Ubiquitin ligase - Wikipedia

    en.wikipedia.org/wiki/Ubiquitin_ligase

    A ubiquitin ligase (also called an E3 ubiquitin ligase) is a protein that recruits an E2 ubiquitin-conjugating enzyme that has been loaded with ubiquitin, recognizes a protein substrate, and assists or directly catalyzes the transfer of ubiquitin from the E2 to the protein substrate. In simple and more general terms, the ligase enables movement ...