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
\[ CH_3Br + OH^- \rightarrow CH_3OH + Br^- \]
Write the IUPAC name of the product formed in the Reimer-Tiemann reaction.
(b) Order of the differential equation: $ 5x^3 \frac{d^3y}{dx^3} - 3\left(\frac{dy}{dx}\right)^2 + \left(\frac{d^2y}{dx^2}\right)^4 + y = 0 $