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SN1 reaction
From Proteopedia
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== S<sub>N</sub>1-Substitution of Cl<sup>-</sup> and ''tert''-Butanol == | == S<sub>N</sub>1-Substitution of Cl<sup>-</sup> and ''tert''-Butanol == | ||
| - | <StructureSection load='' size='340' side='right' caption='' scene='54/542276/Side_view/ | + | <StructureSection load='' size='340' side='right' caption='' scene='54/542276/Side_view/3'> |
The S<sub>N</sub>1 reaction belongs to the basic reaction in organic chemistry. The number 1 says that it is a monomolecular reaction. This means that in the rate determining step of the reaction, only one of the educts is involved. The kinetic of the reaction therefore follows the reation rate of first order. | The S<sub>N</sub>1 reaction belongs to the basic reaction in organic chemistry. The number 1 says that it is a monomolecular reaction. This means that in the rate determining step of the reaction, only one of the educts is involved. The kinetic of the reaction therefore follows the reation rate of first order. | ||
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===See also=== | ===See also=== | ||
| - | [[SN2_reaction|S<sub>N</sub>2 reaction: Substitution of chloride and methanol]] | + | [[SN2_reaction|S<sub>N</sub>2 reaction: Substitution of chloride and methanol]]<br> |
| + | [[Esterification|Esterification]]<br> | ||
| + | [[Ozonolysis|Ozonolysis - a type of cycloaddition]] | ||
== References == | == References == | ||
This demo was adapted from http://www.chemieunterricht-interaktiv.de/en/animations/sn1_substutition/sn1_substitution_3d.html by Dr. V. Pietzner, part of the ChiLe project | This demo was adapted from http://www.chemieunterricht-interaktiv.de/en/animations/sn1_substutition/sn1_substitution_3d.html by Dr. V. Pietzner, part of the ChiLe project | ||
Current revision
SN1-Substitution of Cl- and tert-Butanol
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Proteopedia Page Contributors and Editors (what is this?)
Joel L. Sussman, Jaime Prilusky, Angel Herraez, Verena Pietzner
