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The unimolecular nucleophilic substitution (SN1) reaction is a substitution reaction in organic chemistry. The Hughes-Ingold symbol of the mechanism expresses two properties—"SN" stands for "nucleophilic substitution", and the "1" says that the rate-determining step is unimolecular. Thus, the rate equation is often shown as having first-order dependence…
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reaction carbocation nucleophile sn1 rate step mechanism alkyl nucleophilic conditions intermediate ion side often sn2 first substitution water reactions leaving
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| SN1 reaction | is a | ionization of alkyl halide in the presence of aqueous acetone or ethyl alcohol | 0.90 | text |
| hydroxide or methoxide ion | instance of | If an attempt is made to perform an SN1 reaction using a strongly basic nucleophile | 0.80 | text |
| the alkene will again be formed | instance of | If an attempt is made to perform an SN1 reaction using a strongly basic nucleophile | 0.80 | text |
| this time via an E2 elimination | instance of | If an attempt is made to perform an SN1 reaction using a strongly basic nucleophile | 0.80 | text |
| SN1 reaction | has effect | Since | 0.60 | section |
| SN1 reaction | has effect | SN1 | 0.60 | section |
| SN1 reaction | has effect | RDS | 0.60 | section |
| SN1 reaction | has effect | The | 0.60 | section |
| SN1 reaction | has effect | Typical | 0.60 | section |
| SN1 reaction | related to Mechanism | An | 0.60 | section |
| SN1 reaction | related to Mechanism | SN1 | 0.60 | section |
| SN1 reaction | related to Mechanism | This SN1 | 0.60 | section |
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