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प्रश्न
Draw the resonance structure of the following compounds;
\[\begin{array}{cc}
\ce{CH2 = CH - C = O}\\
\phantom{.........}|\\
\phantom{.........}\ce{H}
\end{array}\]
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संबंधित प्रश्न
Draw the resonance structure for the following compound. Show the electron shift using curved-arrow notation.
\[\ce{C6H5 - \overset{+}{C}H2}\]
Draw the resonance structure for the following compound. Show the electron shift using curved-arrow notation.
\[\ce{CH3CH = CH\overset{+}{C}H2}\]
In which of the following representations given below spatial arrangement of group/ atom different from that given in structure ‘A’?
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(A) |
(i) | ![]() |
(ii) | ![]() |
(iii) | ![]() |
(iv) | ![]() |
Draw the possible resonance structures for \[\ce{CH3 - \overset{\bullet\bullet}{\underset{\bullet\bullet}{O}} - \overset{+}{C}H2}\] and predict which of the structures is more stable. Give reason for your answer.
Which of the following ions is more stable? Use resonance to explain your answer.
Draw the resonance structure of the following compounds;
Draw the resonance structure of the following compounds;
CH2 = CH – CH = CH2
Which of the following compounds will not exist as resonance hybrid. Give reason for your answer:
Which of the two structures (A) and (B) given below is more stabilised by resonance? Explain.
\[\ce{\underset{(A)}{CH3COOH}}\] and \[\ce{\underset{(B)}{CH3CO\overset{Θ}{O}}}\]
Assertion (A): Energy of resonance hybrid is equal to the average of energies of all canonical forms.
Reason (R): Resonance hybrid cannot be presented by a single structure.