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Four structures are given in options (a)...

Four structures are given in options (a) to (d) . Examine them and select the aromatic structures.

A

B

C

D

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To determine which of the given structures are aromatic, we need to follow a systematic approach based on the criteria for aromaticity. Here’s a step-by-step solution: ### Step 1: Understand the Criteria for Aromaticity A compound is considered aromatic if it meets the following criteria: 1. It must be cyclic (ring structure). 2. It must be planar (all atoms in the ring must lie in the same plane). 3. It must have a continuous overlap of p-orbitals (conjugated π-bonds). 4. It must follow Huckel's rule, which states that there should be \(4n + 2\) π electrons, where \(n\) is a non-negative integer (0, 1, 2, ...). ### Step 2: Analyze Each Structure #### Structure A: - **Cyclic**: Yes, it is a ring. - **Planar**: Yes, all carbon atoms are sp² hybridized, making them planar. - **Conjugated π-bonds**: Yes, there are π-bonds that can delocalize. - **Count π electrons**: There are 2 π electrons. - Applying Huckel's rule: \(4n + 2 = 2\) (where \(n = 0\)). - This satisfies Huckel's rule. **Conclusion**: Structure A is aromatic. #### Structure B: - **Cyclic**: Yes, it is a ring. - **Planar**: Yes, all carbon atoms are sp² hybridized. - **Conjugated π-bonds**: Yes, there are π-bonds. - **Count π electrons**: There are 8 π electrons. - Applying Huckel's rule: \(4n + 2 = 8\) (no integer \(n\) satisfies this). **Conclusion**: Structure B is not aromatic. #### Structure C: - **Cyclic**: Yes, it is a ring. - **Planar**: Yes, all carbon atoms are sp² hybridized. - **Conjugated π-bonds**: Yes, there are π-bonds. - **Count π electrons**: There are 12 π electrons. - Applying Huckel's rule: \(4n + 2 = 12\) (no integer \(n\) satisfies this). However, if we consider the individual rings, one of the rings may still be aromatic. - The first ring has 6 π electrons (satisfies Huckel's rule). **Conclusion**: Structure C is aromatic because at least one of its rings is aromatic. #### Structure D: - **Cyclic**: Yes, it is a ring. - **Planar**: Yes, all atoms are in the same plane. - **Conjugated π-bonds**: Yes, there are π-bonds. - **Count π electrons**: There are 4 π electrons. - Applying Huckel's rule: \(4n + 2 = 4\) (no integer \(n\) satisfies this). **Conclusion**: Structure D is not aromatic. ### Final Answer: The aromatic structures are **A and C**. ---

To determine which of the given structures are aromatic, we need to follow a systematic approach based on the criteria for aromaticity. Here’s a step-by-step solution: ### Step 1: Understand the Criteria for Aromaticity A compound is considered aromatic if it meets the following criteria: 1. It must be cyclic (ring structure). 2. It must be planar (all atoms in the ring must lie in the same plane). 3. It must have a continuous overlap of p-orbitals (conjugated π-bonds). 4. It must follow Huckel's rule, which states that there should be \(4n + 2\) π electrons, where \(n\) is a non-negative integer (0, 1, 2, ...). ...
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