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.
List-I | List-II | ||
(A) | [Co(NH3)5(NO2)]Cl2 | (I) | Solvate isomerism |
(B) | [Co(NH3)5(SO4)]Br | (II) | Linkage isomerism |
(C) | [Co(NH3)6] [Cr(CN)6] | (III) | Ionization isomerism |
(D) | [Co(H2O)6]Cl3 | (IV) | Coordination isomerism |