sn1 reaction explain
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An Sn1 reaction is a reaction that depends on the substrate and it is a 2-step process.
1. Departure of the leaving group and the formation of carbocation intermediate
2. A weak nucleophile comes in and inserts itself into the compound
They normally occur in polar protic solvents and they generally favor stable carbocations so tertiary > secondary > primary > methyl
For example, let us say you have 2-bromo-2-methylpropane. The rate determining step is the dissociation of this species into a positively charged ion. (CH3)C+ is the carbocation and the LG is Br-
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it is a nucleophilic substitution reaction which involves two step first rate determination which is slow hindrance effect may effect the reaction
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