In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?
and
In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?
Greater the stability of the carbocation, faster is the rate of SN1 reaction. Since secondary carbocation 2-chloroheptane is more stable than primary carbocation 1-chlorohexane. Hence SN2 reaction proceed via secondary cation such as 2-chloroheptane.
Thionyl chloride is preferred in the preparation of chloro alkanes from alcohol. Give reason.