



The following reactions are analyzed:
1. Reaction (1):

This reaction illustrates the hydrolysis of acetyl chloride, an acyl chloride, yielding acetic acid, a carboxylic acid. This is a typical reaction, as acyl chlorides readily react with water to produce carboxylic acids.
2. Reaction (2):
This reaction shows an incorrect attempt to reduce benzamide to benzoic acid using lithium aluminum hydride (LiAlH4). LiAlH4 is a potent reducing agent that converts amides to amines, not carboxylic acids. The expected product is benzylamine.
3. Reaction (3):
This reaction depicts the oxidation of ethanol to acetic acid using alkaline potassium permanganate (KMnO₄), followed by acidification. This is a standard oxidation process.
4. Reaction (4):
This reaction demonstrates the oxidation of propanol to propanoic acid using a combination of chromium trioxide (CrO₃) and sulfuric acid (H₂SO₄). This is also a standard oxidation reaction.
The correct order of the rate of reaction of the following reactants with nucleophile by \( \mathrm{S_N1} \) mechanism is:
(Given: Structures I and II are rigid) 