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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 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. **Planarity**: The molecule must be planar, allowing for effective overlap of p-orbitals. 2. **Conjugated Double Bonds**: The molecule must have a continuous ring of p-orbitals, which typically means alternating single and double bonds. 3. **Hückel's Rule**: The molecule must have \(4n + 2\) π electrons, where \(n\) is a non-negative integer (0, 1, 2, ...). ### Step 2: Analyze Each Structure Let’s examine each structure one by one based on the criteria above. #### Structure 1: Cyclopropene with a Positive Charge - **Planarity**: Yes, all carbons are sp² hybridized. - **Conjugation**: There is one double bond, but it does not have conjugated double bonds. - **π Electrons**: There are 2 π electrons (for \(n = 0\), \(4(0) + 2 = 2\)). - **Conclusion**: This structure is aromatic. #### Structure 2: A Compound with 8 π Electrons - **Planarity**: Yes, all carbons are sp² hybridized. - **Conjugation**: There are conjugated double bonds. - **π Electrons**: There are 8 π electrons (for \(n = 2\), \(4(2) + 2 = 10\)). - **Conclusion**: This structure is anti-aromatic (not aromatic). #### Structure 3: Bifenyl - **Planarity**: Yes, both benzene rings are planar and sp² hybridized. - **Conjugation**: Each benzene ring has conjugated double bonds. - **π Electrons**: Each benzene ring has 6 π electrons (for \(n = 1\), \(4(1) + 2 = 6\)). - **Conclusion**: This structure is aromatic. #### Structure 4: A Compound with 4 π Electrons - **Planarity**: Yes, all carbons are sp² hybridized. - **Conjugation**: There are conjugated double bonds. - **π Electrons**: There are 4 π electrons (for \(n = 1\), \(4(1) + 2 = 6\)). - **Conclusion**: This structure is anti-aromatic (not aromatic). ### Final Conclusion The aromatic structures from the given options are: - **Structure 1 (Cyclopropene with a Positive Charge)** - **Structure 3 (Bifenyl)**

To determine which of the given structures are aromatic, we need to follow 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. **Planarity**: The molecule must be planar, allowing for effective overlap of p-orbitals. 2. **Conjugated Double Bonds**: The molecule must have a continuous ring of p-orbitals, which typically means alternating single and double bonds. 3. **Hückel's Rule**: The molecule must have \(4n + 2\) π electrons, where \(n\) is a non-negative integer (0, 1, 2, ...). ...
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