Chlorobenzene when treated with ethanolic `AgNO_(3)` it does not give white precipitate. Explain.

Explanation

**Step-by-Step Solution:**

1. **Understanding the Reaction Context**: Chlorobenzene (C6H5Cl) is an aromatic compound where a chlorine atom is bonded to a benzene ring. When treated with ethanolic AgNO3, we expect a reaction that could lead to the formation of AgCl, which is a white precipitate.

2. **Nature of the Bond**: In chlorobenzene, the carbon-chlorine (C-Cl) bond exhibits partial double bond character due to resonance. The benzene ring can delocalize electrons, which stabilizes the C-Cl bond and makes it stronger than a typical single bond found in aliphatic haloalkanes.

3. **Resonance Structures**: The resonance structures of chlorobenzene show that the chlorine atom has a partial positive charge and the carbon atom has a partial negative charge. This stabilization through resonance means that the C-Cl bond does not easily break.

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