What is correct for resonance structure ?
The cannonical forms have no real existence.
The molecule does not exist for a certain fraction of time in one cannonical forms. There is no such equilibrium between the cannonical forms as we have between tautomeric form in tautomerism.
The molecule as such has a single structure which is the resonance hybrid of the cannonical form and which cannot as such be depicted by a single Lewis structure.
How many $\sigma $ and $\pi $ bonds are there in the molecule of tetracyanoethylene
$\begin{array}{*{20}{c}} {N \equiv C} \\ {N \equiv C}\end{array}\,\,\left. {} \right\rangle C = C\,\left\langle {} \right.\,\begin{array}{*{20}{c}} {C \equiv N} \\ {C \equiv N} \end{array}$
All bond lengths are identical in :-
Give resonance of ${{\rm{O}}_3}$, And Explain its requirement, delimitation and advantages
Choose the $CORRECT$ comparison of decreasing $\pi -$ bond order of $S-O$ bond ?
Among the species : $C{O_2},C{H_3}CO{O^ - },$ $CO,C{O_3}^{2 - },$ $HCHO$ which has the weakest carbon- oxygen bond