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  2. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    Elimination reactions are usually favoured at elevated temperatures [15] because of increased entropy. This effect can be demonstrated in the gas-phase reaction between a phenolate and a simple alkyl bromide taking place inside a mass spectrometer: [16] [17] Competition experiment between SN2 and E2

  3. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    With standard S N 1 reaction conditions the reaction outcome is retention via a competing S N i mechanism and not racemization and with pyridine added the result is again inversion. [5] [3] S N i reaction mechanism Sn1 occurs in tertiary carbon while Sn2 occurs in primary carbon

  4. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    If the reaction is performed under warm or hot conditions (which favor an increase in entropy), E1 elimination is likely to predominate, leading to formation of an alkene. At lower temperatures, S N 1 and E1 reactions are competitive reactions and it becomes difficult to favor one over the other. Even if the reaction is performed cold, some ...

  5. 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).

  6. Category:Nucleophilic substitution reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Nucleophilic...

    Download as PDF; Printable version; In other projects ... SN1 reaction; SN1CB mechanism; SN2 reaction; SNi This page was ...

  7. File:Sn2 reaction IBO IRC.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Sn2_reaction_IBO_IRC.pdf

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  8. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    This reaction differs from a common S N 2 reaction, because it happens at a trigonal carbon atom (sp 2 hybridization). The mechanism of S N 2 reaction does not occur due to steric hindrance of the benzene ring. In order to attack the C atom, the nucleophile must approach in line with the C-LG (leaving group) bond from the back, where the ...

  9. File:Aromatic SN1 mechanism.svg - Wikipedia

    en.wikipedia.org/wiki/File:Aromatic_SN1...

    Category:Chemical reactions *Description: Mechanism of aromatic SN1 reaction (aromatic nucleophilic substitution). *Source = Own work. *Date = 25 Dec 2007. *Made with ...