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
\[ CH_3Br + OH^- \rightarrow CH_3OH + Br^- \]
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?
Find the values of \( x, y, z \) if the matrix \( A \) satisfies the equation \( A^T A = I \), where
\[ A = \begin{bmatrix} 0 & 2y & z \\ x & y & -z \\ x & -y & z \end{bmatrix} \]