Step 1: Types of Nucleophilic Substitution 1. SN1 Mechanism (Unimolecular)
- Two-step process involving a carbocation intermediate. 2. SN2 Mechanism (Bimolecular)
- One-step reaction with a transition state.
Step 2: Example - Hydrolysis of Methyl Bromide
\[ CH_3Br + OH^- \rightarrow CH_3OH + Br^- \]
Arrange the following compounds in increasing order of their boiling points:

The reaction 
suggests that phenol is :
In the reaction R–OH + HCl $\xrightarrow{\text{ZnCl}_2}$ RCl + H$_2$O, what is the correct order of reactivity of alcohols?