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overset(Theta)(C)H(3) is less stable tha...

`overset(Theta)(C)H_(3)` is less stable than

A

`CH_(3)-overset(Theta)(C)H_(2)`

B

`CH_(3)-overset(Theta)(C)H-CH_(3)`

C

`overset(Theta)(C)H_(2)-NO_(2)`

D

`CH_(3)-overset(Theta)(C)H-C_(2)H_(5)`

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The correct Answer is:
To determine which species is more stable than the methyl anion (CH3-), we need to analyze the stability of different anions based on the inductive effect and resonance. ### Step-by-Step Solution: 1. **Identify the Anion in Question**: We start with the methyl anion (CH3-). This anion has a negative charge on a carbon atom, which makes it less stable due to the high electronegativity of carbon. 2. **Consider the Stability Factors**: The stability of anions can be influenced by: - Inductive effects (electron-donating or electron-withdrawing groups) - Resonance effects (delocalization of charge) 3. **Compare with Other Anions**: - **CH3- vs. CH2- (from CH3-CH2)**: The ethyl anion (CH2-) has an alkyl group (CH3) that can donate electron density through the +I effect. This means that CH2- is more stable than CH3- because the additional alkyl group helps to stabilize the negative charge by donating electron density. - **CH3- vs. CH2- (from CH3-CH2-CH3)**: In this case, the negative charge is on a carbon that is bonded to two other carbon atoms (CH2-). The presence of two alkyl groups means more electron donation, which stabilizes the negative charge further compared to CH3-. - **CH3- vs. CH2- with Electron-Withdrawing Groups**: If we introduce an electron-withdrawing group like NO2 attached to a carbon adjacent to the negatively charged carbon, it will stabilize the anion by pulling electron density away from the negatively charged carbon. This makes the anion more stable than CH3-. 4. **Conclusion**: After analyzing the stability based on the inductive and resonance effects, we conclude that CH3- is less stable than anions that have electron-donating groups (like CH2-) and more stable than those with strong electron-withdrawing groups (like NO2). ### Final Answer: The methyl anion (CH3-) is less stable than CH2- (from CH3-CH2) and CH2- with an electron-withdrawing group like NO2.
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BANSAL-GENERAL ORGANIC CHEMISTRY-Exercise 3
  1. overset(Theta)(C)H(3) is less stable than

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  2. Write stability order of following intermediates:

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  3. Write stability order of following intermediates:

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  4. Write Stability order of following intermediates:

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  5. Rank the following sets of intermediates in increasing order of their ...

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  6. In each of the following pairs of ions which ion is more stable:

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  7. Rank the following sets of intermediates in increasing order of their ...

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  8. Rank the following sets of intermediates in increasing order of their ...

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  9. Compare heat of hydrogenation (Decreasing order)

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  10. Write increasing order of heat of hydrogenation:

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  11. In which of the following pairs, indicated bond is of greater strength...

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  12. Consider the given reaction: In the above reaction which one of t...

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  13. Write correct order of acidic strength of following compounds: (i). ...

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  14. Write increasing order of basic strength of following: (i). (a) F^(ɵ...

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  15. Record the following sets of compounds according to increasing pK(a)(=...

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  16. Explain which is a stronger acid CH(3)CH(3)&BrCH(2)NO(2)

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  17. Which of the following pairs has higher resonance energy: (a). CH(3)...

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  18. Choose the more stable alkene in each of the following pair. Explain y...

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  19. Which of the followig pairs has higher resonance energy: (a). (b)...

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  20. Rank the following sets of intermediates in increasing order of their ...

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