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  2. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    The bimolecular nucleophilic substitution (S N 2) is a type of reaction mechanism that is common in organic chemistry. In the S N 2 reaction, a strong nucleophile forms a new bond to an sp 3-hybridised carbon atom via a backside attack, all while the leaving group detaches from the reaction center in a concerted (i.e. simultaneous) fashion.

  3. 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 ...

  4. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    The difference between S N 1 and S N i is actually that the ion pair is ... S N i reaction mechanism Sn1 occurs in tertiary carbon while Sn2 occurs in primary carbon ...

  5. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    The Hughes-Ingold symbol of the mechanism expresses two properties—"S N" stands for "nucleophilic substitution", and the "1" says that the rate-determining step is unimolecular. [1] [2] Thus, the rate equation is often shown as having first-order dependence on the substrate and zero-order dependence on the nucleophile. This relationship holds ...

  6. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    A hydroxide ion acting as a nucleophile in an S N 2 reaction, converting a haloalkane into an alcohol. In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they ...

  7. Associative substitution - Wikipedia

    en.wikipedia.org/wiki/Associative_substitution

    V = z 1 z 2 e 2 /4πaε Where z is the charge number of each species and ε is the vacuum permittivity . A typical value for K E is 0.0202 dm 3 mol −1 for neutral particles at a distance of 200 pm. [ 9 ] The result of the rate law is that at high concentrations of Y, the rate approximates k[M] tot while at low concentrations the result is kK ...

  8. Woman Attempting to Smuggle 22 Pounds of Meth Wrapped as ...

    www.aol.com/lifestyle/woman-attempting-smuggle...

    The seized drug would have been worth up to NZ$3.8 million, about $2.2 million USD, said the New Zealand Customs Service in a news release Woman Attempting to Smuggle 22 Pounds of Meth Wrapped as ...

  9. Double electron capture - Wikipedia

    en.wikipedia.org/wiki/Double_electron_capture

    If the mass difference between the mother and daughter atoms is more than two masses of an electron (1.022 MeV), the energy released in the process is enough to allow another mode of decay, called electron capture with positron emission. It occurs along with double electron capture, their branching ratio depending on nuclear properties.