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Karnataka Board PUCPUC Science Class 11

Explain the important aspects of resonance with reference to the COCO32- ion. - Chemistry

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Question

Explain the important aspects of resonance with reference to the `"CO"_3^(2-)` ion.

Answer in Brief

Solution 1

Resonance in `"CO"_3^(2-)`, I, II and III represent the three canonical forms.

  • In these structures, the position of nuclei are same.
  • All three forms have almost equal energy.
  • Same number of paired and impaired electrons differ only in their position.
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Solution 2

According to experimental findings, all carbon to oxygen bonds in  `"CO"_3^(2-)` are equivalent. Hence, it is inadequate to represent  `"CO"_3^(2-)` ion by a single Lewis structure having two single bonds and one double bond.

Therefore, carbonate ion is described as a resonance hybrid of the following structures

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Chapter 4: Chemical Bonding and Molecular Structure - EXERCISES [Page 134]

APPEARS IN

NCERT Chemistry - Part 1 and 2 [English] Class 11
Chapter 4 Chemical Bonding and Molecular Structure
EXERCISES | Q 4.11 | Page 134

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H3PO3 can be represented by structures 1 and 2 shown below. Can these two structures be taken as the canonical forms of the resonance hybrid representing H3PO3? If not, give reasons for the same.

(1) (2)

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Draw the resonating structure of ozone molecule


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Resonance structures can be written for ______.


The acceptable resonating structures of the following molecule are:

\[\begin{array}{cc}
\ce{CH3 - CH = C - \overset{\bullet\bullet}{\underset{\bullet\bullet}{O}} - CH2 - CH3}\\
|\phantom{......}\\
\ce{:N}\phantom{.......}\\
\phantom{}/\phantom{...}\backslash\phantom{......}\\
\phantom{}\ce{H3C}\phantom{.....}\ce{CH3}\phantom{......}
\end{array}\]

(x) \[\begin{array}{cc}
\ce{CH3 - \overset{\overset{Θ}{\bullet\bullet}}{C}H - C -  \overset{\bullet\bullet}{\underset{\bullet\bullet}{O}} - CH2 - CH3}\\
||\phantom{......}\\
\ce{N^⊕}\phantom{.....}\\
\phantom{}/\phantom{...}\backslash\phantom{......}\\
\phantom{}\ce{H3C}\phantom{.....}\ce{CH3}\phantom{......}
\end{array}\]
(y) \[\begin{array}{cc}
\ce{CH3 - \overset{\overset{Θ}{\bullet\bullet}}{C}H - C =  \overset{⊕}{\underset{\bullet\bullet}{O}} - CH2 - CH3}\\
|\phantom{......}\\
\ce{:N}\phantom{.......}\\
\phantom{}/\phantom{...}\backslash\phantom{......}\\
\phantom{}\ce{H3C}\phantom{.....}\ce{CH3}\phantom{......}
\end{array}\]
(z) \[\begin{array}{cc}
\ce{CH3 - \overset{⊕}{C}H - C -  \overset{\bullet\bullet}{\underset{\bullet\bullet}{O}} - CH2 - CH3}\\
||\phantom{......}\\
\ce{N^Θ}\phantom{.....}\\
\phantom{}/\phantom{...}\backslash\phantom{......}\\
\phantom{}\ce{H3C}\phantom{.....}\ce{CH3}\phantom{......}
\end{array}\]
(w) \[\begin{array}{cc}
\ce{CH3 - \overset{⊕}{C}H - C =  \overset{Θ}{O} - CH2 - CH3}\\
|\phantom{......}\\
\ce{:N}\phantom{.......}\\
\phantom{}/\phantom{...}\backslash\phantom{......}\\
\phantom{}\ce{H3C}\phantom{.....}\ce{CH3}\phantom{......}
\end{array}\]

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