(A) Due to the delocalization of $\pi$ electrons,benzene exhibits resonance. This resonance leads to the formation of hybrid structures where all $C

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(A) Due to the delocalization of $\pi$ electrons,benzene exhibits resonance. This resonance leads to the formation of hybrid structures where all $C - C$ bonds have partial double bond character. Consequently,the bond length is intermediate between a pure single bond $(1.54 \ \mathring{A})$ and a pure double bond $(1.34 \ \mathring{A})$.

Class 11 Chemistry Chemical Bonding and Molecular Structure Resonance

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The $C - C$ bond length in benzene lies between a single and a double bond. The reason is:

A
Resonance
B
Isomerism
C
Metamerism
D
Inductive effect

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Class 11

Chemistry Questions

Chapter

Chemical Bonding and Molecular Structure

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Resonance

How many resonance forms can be written for the nitrate ion,$(NO_3^-)$?

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$CH_3-C(=O)-OCH_3$. In the given structure,the bond between carbonyl carbon and oxygen is $a$ and the bond between oxygen and methyl group is $b$. The correct relation between the bond lengths $a$ and $b$ is:

Medium

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Explain the important aspects of resonance with reference to the $CO_{3}^{2-}$ ion.

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Which of the following conditions is not correct for resonating structures?

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Consider the following three resonance structures:
The correct order of their stabilities is:

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The $C - C$ bond length in benzene lies between a single and a double bond. The reason is:

Similar Questions

How many resonance forms can be written for the nitrate ion,$(NO_3^-)$?

$CH_3-C(=O)-OCH_3$. In the given structure,the bond between carbonyl carbon and oxygen is $a$ and the bond between oxygen and methyl group is $b$. The correct relation between the bond lengths $a$ and $b$ is:

Explain the important aspects of resonance with reference to the $CO_{3}^{2-}$ ion.

Which of the following conditions is not correct for resonating structures?

Consider the following three resonance structures:The correct order of their stabilities is:

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Consider the following three resonance structures:
The correct order of their stabilities is: