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  2. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    The C-H bond is weakened in the rate determining step and therefore a primary deuterium isotope effect much larger than 1 (commonly 2-6) is observed. E2 competes with the S N 2 reaction mechanism if the base can also act as a nucleophile (true for many common bases). Scheme 1: E2 reaction mechanism. An example of this type of reaction in scheme ...

  3. Leaving group - Wikipedia

    en.wikipedia.org/wiki/Leaving_group

    The requirement for a good leaving group is still relaxed in the case of C=C bond formation via E1cB mechanisms, but because of the relative weakness of the C=C double bond, the reaction still exhibits some leaving group sensitivity. Notably, changing the leaving group's identity (and willingness to leave) can change the nature of the mechanism ...

  4. 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.

  5. Zaytsev's rule - Wikipedia

    en.wikipedia.org/wiki/Zaytsev's_rule

    For example, when 2-iodobutane is treated with alcoholic potassium hydroxide (KOH), but-2-ene is the major product and but-1-ene is the minor product. [1] More generally, Zaytsev's rule predicts that in an elimination reaction the most substituted product will be the most stable, and therefore the most favored.

  6. Activation strain model - Wikipedia

    en.wikipedia.org/wiki/Activation_strain_model

    The activation strain model was originally proposed and has been extensively developed by Bickelhaupt and coworkers. [4] This model breaks the potential energy curve as a function of reaction coordinate, ζ, of a reaction into 2 components as shown in equation 1: the energy due to straining the original reactant molecules (∆E strain) and the energy due to interaction between reactant ...

  7. Kinetic isotope effect - Wikipedia

    en.wikipedia.org/wiki/Kinetic_isotope_effect

    A primary kinetic isotope effect (PKIE) may be found when a bond to the isotopically labeled atom is being formed or broken. [3] [4]: 427 Depending on the way a KIE is probed (parallel measurement of rates vs. intermolecular competition vs. intramolecular competition), the observation of a PKIE is indicative of breaking/forming a bond to the isotope at the rate-limiting step, or subsequent ...

  8. Reactivity (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Reactivity_(chemistry)

    For example, it is commonly asserted that the reactivity of alkali metals (Na, K, etc.) increases down the group in the periodic table, or that hydrogen's reactivity is evidenced by its reaction with oxygen. In fact, the rate of reaction of alkali metals (as evidenced by their reaction with water for example) is a function not only of position ...

  9. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    One example where the rotamers become significant is elimination reactions, which involve the simultaneous removal of a proton and a leaving group from vicinal or antiperiplanar positions under the influence of a base. Base-induced bimolecular dehydrohalogenation (an E2 type reaction mechanism).