



Let’s analyze each reaction:
1. Reaction (1):

This reaction shows the hydrolysis of an acyl chloride (acetyl chloride) to a carboxylic acid (acetic acid). This is a standard reaction. Acyl chlorides readily react with water to form carboxylic acids.
2. Reaction (2):
This reaction depicts the attempted reduction of benzamide to benzoic acid using lithium aluminum hydride (LiAlH4). This is incorrect. LiAlH4 is a strong reducing agent that reduces amides to amines, not carboxylic acids. The correct product would be benzylamine.
3. Reaction (3):
This reaction shows the oxidation of ethanol to acetic acid using alkaline potassium permanganate (KMnO₄), followed by acidification. This is a standard oxidation reaction.
4. Reaction (4):
This reaction shows the oxidation of propanol to propanoic acid using a mixture 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) 
| LIST I | LIST II | ||
|---|---|---|---|
| A | Lyman | I | Near IR |
| B | Balmer | II | Far IR |
| C | Paschen | III | Visible |
| D | p-fund | IV | UV |
What is Microalbuminuria ?
The output (Y) of the given logic implementation is similar to the output of an/a …………. gate.