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A trisubstituted compound 'A' C(10)H(12)...

A trisubstituted compound 'A' `C_(10)H_(12)O_2` gives neutral `FeCl_3` test positive.Treatment of compound 'A' with `NaOH` and `CH_(3)Br` gives `C_(11)H_(14)O_(2)`,with hydrodioic acid gives methyl iodide and with hot conc. `NaOH` gives a compound `B,C_(10)H_(12)O_(2),C` Compound '`A`' also decolorises alkaline `KMnO_4`. The number of `pi` bond's present in the compound '`A`' is

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To solve the problem, we need to analyze the information given about compound 'A' and deduce the number of π bonds present in it. ### Step-by-Step Solution: 1. **Identify the Structure of Compound 'A':** - The molecular formula of compound 'A' is C₁₀H₁₂O₂. - It gives a positive neutral FeCl₃ test, indicating the presence of a phenolic (aromatic) group, which means it likely contains an -OH group attached to a benzene ring. 2. **Determine the Degree of Unsaturation:** - The degree of unsaturation (DU) can be calculated using the formula: \[ \text{DU} = \frac{(2C + 2 + N - H - X)}{2} \] - For compound 'A': C = 10, H = 12, O = 2 (O does not affect the calculation). - Plugging in the values: \[ \text{DU} = \frac{(2 \times 10 + 2 - 12)}{2} = \frac{(20 + 2 - 12)}{2} = \frac{10}{2} = 5 \] - This indicates that there are 5 degrees of unsaturation, which can be due to rings and/or π bonds. 3. **Analyze Possible Structures:** - Since compound 'A' is trisubstituted and contains a phenolic group, it likely has a benzene ring (which contributes 3 π bonds). - The remaining degrees of unsaturation could come from: - A carbonyl group (C=O) which contributes 1 π bond. - Therefore, the total number of π bonds in compound 'A' can be calculated as: \[ \text{Total π bonds} = 3 \text{ (from benzene)} + 1 \text{ (from carbonyl)} = 4 \] 4. **Conclusion:** - The number of π bonds present in compound 'A' is 4. ### Final Answer: The number of π bonds present in compound 'A' is **4**. ---
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