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Identify the odd species out Which of th...

Identify the odd species out Which of the species among the following is different from others ?

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To solve the problem of identifying the odd species out among the given options based on their aromatic or anti-aromatic nature, we will follow these steps: ### Step 1: Understand the Criteria for Aromaticity and Anti-aromaticity - **Aromatic Compounds** must satisfy the following conditions: 1. The molecule must be cyclic. 2. The molecule must be planar. 3. The molecule must follow Huckel's rule, which states that it must have \(4n + 2\) π electrons, where \(n\) is a non-negative integer (0, 1, 2, ...). - **Anti-aromatic Compounds** must satisfy: 1. The molecule must be cyclic. 2. The molecule must be planar. 3. The molecule must have \(4n\) π electrons. ### Step 2: Analyze Each Option Let's analyze the given options one by one to determine whether they are aromatic or anti-aromatic. #### Option 1: Cyclobutadiene - Structure: Cyclic with 4 π electrons (2 double bonds). - Analysis: - Cyclic: Yes - Planar: Yes - π Electrons: 4 (follows \(4n\) rule, where \(n=1\)). - Conclusion: **Anti-aromatic** #### Option 2: Cyclobutene - Structure: Cyclic with 4 π electrons (2 double bonds). - Analysis: - Cyclic: Yes - Planar: Yes - π Electrons: 4 (follows \(4n\) rule, where \(n=1\)). - Conclusion: **Anti-aromatic** #### Option 3: Cyclopentadienyl Anion - Structure: Cyclic with 6 π electrons (2 double bonds + 1 lone pair). - Analysis: - Cyclic: Yes - Planar: Yes - π Electrons: 6 (follows \(4n + 2\) rule, where \(n=1\)). - Conclusion: **Aromatic** #### Option 4: Benzene - Structure: Cyclic with 6 π electrons (3 double bonds). - Analysis: - Cyclic: Yes - Planar: Yes - π Electrons: 6 (follows \(4n + 2\) rule, where \(n=1\)). - Conclusion: **Aromatic** ### Step 3: Identify the Odd Species From our analysis: - Option 1 (Cyclobutadiene) and Option 2 (Cyclobutene) are **anti-aromatic**. - Option 3 (Cyclopentadienyl Anion) and Option 4 (Benzene) are **aromatic**. Thus, the odd species out is **Option 1: Cyclobutadiene**, as it is the only one that is anti-aromatic. ### Final Answer The odd species out is **Cyclobutadiene**. ---
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MOTION-GOC-Exercise - 2 (Level - I)
  1. There are three canonical structures of napthalene. Examine them and f...

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  2. Which of the following has longest C – O bond:

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  3. Among the following molecules, the correct order of C - C bond length ...

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  4. In which of the following molecules pi-electron density in ring is max...

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  5. Which of these cyclopropene systems is aromatic

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  6. Which of these species is anti-aromatic ?

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  7. Which of the following compouds is not aromatic

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  8. The most stable canonical structure of this molecule is

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  9. The most stable canonical structure of this molecule is

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  10. The barrier for rotation about the indicated bonds Will be maximum i...

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  11. Identify the odd species out Which of the species among the following ...

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  12. Which of the following heterocyclic compounds would have aromatic char...

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  13. Which one of the following carbonyl compound when treated with dilute ...

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  14. The order of the rate of formation of carbocations from the following ...

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  15. Write correct order of reactivity of following halogen derivatives tow...

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  16. Which of the following species is not aromatic ?

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  17. The aromatic character is maximum in which of these three compounds ?

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  18. underset((I))(CH(3)COOH)" "underset((II))(CH(3)COONa)" "underset...

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  19. Among these compounds, which one has maximum resonance energy ?

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  20. Which of the following orders is correct for the resonance energy of t...

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