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Which of the following will show aromati...

Which of the following will show aromatic behaviour ?

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To determine which of the given compounds shows aromatic behavior, we need to apply Huckel's rule and 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. **Cyclic Structure**: The compound must be a ring. 2. **Planarity**: The compound must be planar, allowing for overlapping p-orbitals. 3. **Conjugation**: There must be a complete cyclic conjugation of pi electrons. 4. **Huckel's Rule**: The compound must have (4n + 2) pi electrons, where n is a non-negative integer (0, 1, 2, ...). ### Step 2: Analyze Each Compound Let’s analyze the compounds one by one: #### Compound 1: - **Cyclic**: Yes, it is cyclic. - **Planar**: Check if all atoms are sp2 hybridized. - **Conjugation**: Look for alternating double bonds. - **Pi Electrons**: Count the pi electrons and check if they fit Huckel's rule. **Conclusion**: This compound does not have complete cyclic conjugation, so it is **not aromatic**. #### Compound 2: - **Cyclic**: Yes, it is a benzene ring. - **Planar**: All carbon atoms in benzene are sp2 hybridized. - **Conjugation**: Benzene has complete conjugation with alternating double bonds. - **Pi Electrons**: Benzene has 6 pi electrons (C6H6), which fits Huckel's rule (4n + 2, where n=1). **Conclusion**: This compound is **aromatic**. #### Compound 3: - **Cyclic**: Yes, it is cyclic. - **Planar**: Check the hybridization of the atoms. - **Conjugation**: Look for alternating double bonds. - **Pi Electrons**: Count the pi electrons. **Conclusion**: If all atoms are sp3 hybridized and there are no pi bonds, this compound is **not aromatic**. #### Compound 4: - **Cyclic**: Yes, it is cyclic. - **Planar**: Check the hybridization. - **Conjugation**: Look for pi bonds. - **Pi Electrons**: Count the pi electrons. **Conclusion**: If it has 4 pi electrons and does not fit Huckel's rule, it is **not aromatic**. ### Final Conclusion Among the given compounds, only **Compound 2 (benzene)** shows aromatic behavior.
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DISHA PUBLICATION-ORGANIC CHEMISTRY SOME BASIC PRINCIPLES AND TECHNIQUES -Exercise - 1 : Concept Builder (Topicwise) TOPIC 3 : Concepts of Reaction Mechanism in Organic Compounds and Purification
  1. In which of the following pairs A is more stable than B ?

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  2. Which of the following has the highest nucleophilicity ?

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  3. The increasing order of the boiling points for the following compound ...

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  4. Which of the following compouns has most acidic hydrogen ?

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  5. Polarization of electrons in acrolein may be written as:

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  6. Identify most acidic hydrogen present in the above compound :

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  7. Of the following compounds, which will have a zero dipole moment ?

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  8. Which statement is incorrect in respect of the above reaction ?

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  9. Carbon-carbon double bond lenghth will be maximum in which of the foll...

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  10. The structure of CH(2)=C=CH(2) is :

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  11. Which of the following will show aromatic behaviour ?

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  12. Which of the following reactions cannot proceed by S(N)1 mechaism ?

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  13. Ketene CH2=C=O has

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  14. Which one of the following does not have sp^(2) hybridised carbon ?

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  15. How many pi - bonds are present in naphthalene ?

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  16. The shape of methyl carbanion is similar to that of -

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  17. Which of the following represents the correct order of stability of ca...

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  18. Which one of the following is most reactive towards electrophilic reag...

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  19. The pair of electron in the given carbanion, CH(3)C -= C^(Θ), is prese...

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  20. The major product of dehydraction of the following

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