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  • In the following pairs of halogen compounds, which compound undergoes faster S_N 1 reaction? (i)

10.8      In the following pairs of halogen compounds, which compound undergoes faster S_{N}1 reaction?

      (i)      

                        

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In S_{N}1 reactions, the reaction is processed by the formation of carbocation as an intermediate and this is the rate-determining step for this kind of reaction. So the compound having more stable carbocation will react faster. In the given case 2- chloro-2-methylpropane we have 3^{\circ} carbon whereas in 3- Chloropentane we have 2^{\circ} carbon.

so 2- chloro-2-methylpropane readily undergo SN1 reaction

Posted by

Devendra Khairwa

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