Write `S_N1` mechanism for the hydrolysis of 2-Bromo-2-methyl propane. Why are `S_N1` reactions generally carried in polar protic solvents?

a) Write S_(N)1 mechanism for the hydrolysis of 2-Bromo-2-methyl propane. Why are S_(N)1 reactions generally carried in polar protic solvents?

(a) Write the equations for the steps involved in the S_(N)1 mechanism of hydrolysis of 2-bromo 2 methyl propane. (b) (i) Name the product formed for the reaction of isopropyl iodide on alcoholic KOH. (ii) What is the condition to be satisfied for a compound to be chiral? (c) What is racemic mixtures?

Rate of S_(N^2) reaction is :

Explain the mechanism of S_N1 reaction taking 2-bromo-2-methyl propane (t-butyl bromide)

S_(N)1 reaction of alkyl halides leads to :

S_(N^1) and S_(N^2) reactions are

S_(N)1 mechanism of alkyl halides is favoured by :