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C-C' bond length in benzene lies between...

C-C' bond length in benzene lies between single and double bond. The reason is

A

Resonance

B

Isomerism

C

Metamerism

D

Inductive effect

Text Solution

Verified by Experts

The correct Answer is:
A
Due to delocalisation of `pi` electrons benzene has resonance .
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ERRORLESS-GENERAL ORGANIC CHEMISTRY -NCERT BASED QUESTIONS (Dipole Moment, Resonance and Reaction Intermediates )
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  2. All bonds in benzene are equal due to

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  3. C-C' bond length in benzene lies between single and double bond. The r...

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  4. Arrangements of (CH(3))(3)C-,(CH(3))(2)CH-,CH(3).CH(2)- when attached ...

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  6. The least stable free radical is

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  7. Among the given cation,s the most stable carbonium ions is ?

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  8. In CH(3)CH(2)OH, the bond that undergoes heterolytic cleavage most rea...

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  9. An aromatic among other things should have a pi-electron cloud contain...

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  10. Which is the most stable carbocation

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  11. Hyperconjugation is also known as

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  12. Relative stabilities of the following carbocations will be in the orde...

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  13. Chloroacetic acid is a stronger acid than acetic acid this can be expl...

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  14. Amongst the given structures , which are permissible resonance forms ?

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

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  16. Ionic species are stabilised by the dispersal of charge. Which of the ...

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  17. The strongest acid is :

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  18. Aromatic properties of benzene are proved by

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  20. Which among the following statements are true with respect to electron...

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