`S_(N^(1))` reaction is a first order nucleophilic substitution e.g. `CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)C-Br+H_(2)Oto CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)C-OH+HBr` The concentration of nucleophile does not appear in the rate law expression. Reaction rate k[RX] In a mulptistep organic reaction , the rate-limiting step is the slowest step . Rate determining step is represented by the following energy level diagram: A reaction energy level diagram for an `S_(N^(1))` reaction .The rate limiting step is spontaneous dissociation of an alkyl halide to give a carbocation intermediate: `S^(N^(1))` reaction is :A. single step reactionB. two step reactionC. a reaction involving free radical intermediateD. a reaction involving carbocation intermediate

`S_(N^(1))` reaction is a first order nucleophilic substitution e.g. `

1.	`S_(N^(1))` reaction is a first order nucleophilic substitution e.g. `CH_(3)-overset(CH_(3))overset(\|)underset(CH_(3))underset(\|)C-Br+H_(2)Oto CH_(3)-overset(CH_(3))overset(\|)underset(CH_(3))underset(\|)C-OH+HBr` The concentration of nucleophile does not appear in the rate law expression. Reaction rate k[RX] In a mulptistep organic reaction , the rate-limiting step is the slowest step . Rate determining step is represented by the following energy level diagram: A reaction energy level diagram for an `S_(N^(1))` reaction .The rate limiting step is spontaneous dissociation of an alkyl halide to give a carbocation intermediate: `S^(N^(1))` reaction is :A. single step reactionB. two step reactionC. a reaction involving free radical intermediateD. a reaction involving carbocation intermediate
Answer» Correct Answer - D

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