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The most stable carbanion is :...

The most stable carbanion is :

A

methyl carbanion

B

primary carbanion

C

secondary carbonion

D

tertiary carbanion

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The correct Answer is:
A
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An organic reaction occurs by using reagents called electrophiles and nucleophiles via the formation of some reactive intermediates called carbocations, carbanions, free radicals, carbenes, nitrenes, radical cations, and radical anions. The most stable carbocation is :

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Which of the following is the most stable carbanion intermediate ?

OP TANDON-BASIC PRINCIPLES OF ORGANIC COMPOUNDS (MECHANISM OF ORGANIC REACTIONS)-OBJECTIVE QUESTIONS (Level-A)
  1. In CH(3)CH(2)OH, the bond that undergoes heterolytic cleavage most rea...

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  2. The most stable carbocation is :

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  3. The most stable carbanion is :

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  4. Which of the following ions is most stable?

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  5. In which of the following, homolytic bond fission takes place :

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  6. The temporary effect in which there is a complete transfer of shared p...

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  7. The number of electrons present in the valence shell of carbon of CH(3...

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  8. The number of electrons, present in the valence shell of carbon of car...

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  9. In which of the following compounds the carbon marked with asterisk is...

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  10. Electronegativity of carbon atoms depends upon their state of hybridis...

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  11. The strongest acid amongst the following compound is

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  12. The shape of CH(3)^(+) is ………….

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  13. In which of the following compounds, the C-Cl bond ion-isation shall g...

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  14. Most stable carbocation is:

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  15. Most stable carbocation is:

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  16. The shape of carbanion, [CH(3)]^(-) is :

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  17. Carbon atom in methyl carbocation and methyl carbanion is and hybrid...

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  18. An electrophilic reagent is:

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  19. A nucleophile is:

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  20. Which of the following compounds prossesses the C-H bonds with the low...

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