the prerequisite for an SN2 reaction is
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Explanation:
The rate-determining step of this reaction depends on the interaction between the two species, namely the nucleophile and the organic compound. SN2 reaction mechanism requires the attack of nucleophile from the back side of the carbon atom.
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Answer:
SN2 reaction mechanism requires the attack of nucleophiles from the back side of the carbon atom.
Explanation:
- The SN2 reaction mechanism includes a nucleophilic substitution reaction between a leaving group (often halide groups or other electron-withdrawing groups) and a nucleophile in an organic molecule.
- The SN2 reaction process requires the approach of a nucleophile from the carbon atom's back side. As a result, the product adopts a stereochemical position that is completely opposite to the leaving group. This is known as configuration inversion.
- The following stages occur in the SN2 reaction:
- (1) The back side of δ+ carbon center is attacked by the nucleophile.
- (2) A transition state occurs when a nucleophile makes a bond with a carbon atom.
- (3) The departing group disperses, resulting in the end product.
- The reaction is bimolecular because there are two molecules present in the transition state. As a result, the reaction rate is influenced by the nucleophile and substrate concentrations.
- Because both the nucleophile and the substrate are engaged in the rate-determining step of the SN2, the Rate Law Of The SN2 Is Second Order.
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