Sandbox SN2
From Proteopedia
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==S<sub>N</sub>2-substitution of chloride and methanol== | ==S<sub>N</sub>2-substitution of chloride and methanol== | ||
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| - | <caption>SN2 - Substitution of Cl<sup>-</sup> and Methanol</caption> | ||
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SN2 reaction is a basic reaction type in organic chemistry. The letter S<sub>N</sub> stands for nulceophilic Substitution, the number 2 stands for bimolecular, with both reactions partners are involved in the reaction rate determining step. It also exists an S<sub>N</sub>1 reaction; here, only one reaction partner is involved in this step. On the other side, SN2 reactions are characterized by exchanging substituents. The substituent that leaves the molecule is called leaving group. | SN2 reaction is a basic reaction type in organic chemistry. The letter S<sub>N</sub> stands for nulceophilic Substitution, the number 2 stands for bimolecular, with both reactions partners are involved in the reaction rate determining step. It also exists an S<sub>N</sub>1 reaction; here, only one reaction partner is involved in this step. On the other side, SN2 reactions are characterized by exchanging substituents. The substituent that leaves the molecule is called leaving group. | ||
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and [[User:Veronika Pelekhov | Veronika Pelekhov]]. | and [[User:Veronika Pelekhov | Veronika Pelekhov]]. | ||
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===See also=== | ===See also=== | ||
[[SN1_reaction|S<sub>N</sub>1 reaction: Substitution of Cl<sup>−</sup> and ''tert''-Butanol ]] | [[SN1_reaction|S<sub>N</sub>1 reaction: Substitution of Cl<sup>−</sup> and ''tert''-Butanol ]] | ||
Revision as of 18:35, 18 July 2021
SN2-substitution of chloride and methanol
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See also
SN1 reaction: Substitution of Cl− and tert-Butanol
References
- ↑ Wang Y, Song H, Szabo I, Czako G, Guo H, Yang M. Mode-Specific SN2 Reaction Dynamics. J Phys Chem Lett. 2016 Sep 1;7(17):3322-7. doi: 10.1021/acs.jpclett.6b01457. Epub, 2016 Aug 12. PMID:27505286 doi:http://dx.doi.org/10.1021/acs.jpclett.6b01457
- ↑ ChiLe Web Site
