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Which of the following is the most stabl...

Which of the following is the most stable carbonium or benzenium ion?

A

B

C

D

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To determine which ion is more stable between the carbonium ion and the benzenium ion, we need to analyze the stability of each ion based on the substituents attached to the aromatic ring and their effects on the positive charge. ### Step-by-Step Solution: 1. **Understanding the Ions**: - A **carbonium ion** (or carbocation) is a positively charged carbon atom that can be stabilized by electron-donating groups. - A **benzenium ion** is a type of carbocation that is derived from benzene, where a hydrogen atom is replaced by a positive charge. 2. **Identifying Electron-Donating and Electron-Withdrawing Groups**: - Electron-donating groups (EDGs) stabilize carbocations by increasing electron density. Examples include alkyl groups (like methyl, ethyl). - Electron-withdrawing groups (EWGs) destabilize carbocations by decreasing electron density. An example is the nitro group (NO2). 3. **Analyzing the Effects of Substituents**: - In the given compounds, the presence of the NO2 group is noted. This group is an EWG and will decrease the stability of any carbocation by pulling electron density away from the positively charged carbon. - The position of the methyl group (an EDG) relative to the carbocation is crucial. The closer the EDG is to the positive charge, the greater its stabilizing effect due to inductive effects and hyperconjugation. 4. **Comparing the Stability of the Ions**: - In the first case, the methyl group is farther from the carbocation. - In the second case, the methyl group is closest to the carbocation, providing maximum stabilization. - In the third case, the methyl group is again farther from the carbocation. - In the fourth case, the methyl group is the farthest from the carbocation. 5. **Conclusion**: - Since the methyl group in the second case is closest to the carbonium ion, it exerts the most significant electron-donating effect, making this ion the most stable. - Therefore, the most stable ion among the given options is the **carbonium ion** in the second case. ### Final Answer: The most stable ion is the **carbonium ion** in option **B**. ---

To determine which ion is more stable between the carbonium ion and the benzenium ion, we need to analyze the stability of each ion based on the substituents attached to the aromatic ring and their effects on the positive charge. ### Step-by-Step Solution: 1. **Understanding the Ions**: - A **carbonium ion** (or carbocation) is a positively charged carbon atom that can be stabilized by electron-donating groups. - A **benzenium ion** is a type of carbocation that is derived from benzene, where a hydrogen atom is replaced by a positive charge. ...
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CENGAGE CHEMISTRY ENGLISH-AROMATIC COMPOUNDS AND ALKYL AND ARYL HALIDES -Exercises Single Correct
  1. In which case will SE not be in m- position?

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  2. Which of the folliwng has the highest dipole moment?

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  3. Which of the following is the most stable carbonium or benzenium ion?

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  4. Which of the following ketonic compound is the least stable?

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  5. Which of the following compounds will give curdy precipate with AgNO(3...

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  6. Which of the folliwng compounds is the most reactive towards electroph...

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  7. Which of the folliwng is the most stable species?

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  8. Which of the following in not aromatic in nature?

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  9. Which of the following species will be least stable?

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  10. Which of the follwing compounds will undergo Friedel Creadfts alylatio...

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  11. Which of the following is anti-aromatic in nature?

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  12. Which of the following aromatic compounds is least reactive towards el...

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  13. Which of the folliwng compounds will show faster ArSN^(2) reactions?

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  14. Which of the folliwng is the order of the rate of reaction of C(6)H(6)...

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  15. Which of the folliwng is the correct order of the order of the rate of...

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  16. Which of the following will give SN^(2) mechanism?

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  17. Which of the following compounds gives SN^(1), SN^(2) and SN^(2) mecha...

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  18. Which of the folliwning ether wil always give SN^(2) mechanism in acid...

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  19. Which of the follwoign ether will always give SN^(2) mechanism in acid...

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  20. Which of the following substrates will gave racemised product?

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