In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?
and
Greater the stability of the carbocation, faster is the rate of SN1 reaction. Since tertiary carbocation 2-chloro-2-methylpropane is more stable than secondary carbocation 3-chloropentane. Hence SN1 reaction proceed via tertiary cation such as 2-chloro-2-methylpropane.
In the following pairs of halogen compounds, which compound undergoes faster SN1 reaction?
Thionyl chloride is preferred in the preparation of chloro alkanes from alcohol. Give reason.