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Which of the following ions is more stable? Use resonance to explain your answer.

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प्रश्न

Which of the following ions is more stable? Use resonance to explain your answer.

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उत्तर

Structure (A) is more stable due to resonance. Structure (B) is non-planar and hence it does not undergo resonance. Double bond is more stable within the ring in comparison to outside the ring.

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Fundamental Concepts in Organic Reaction Mechanism - Resonance Structure
  क्या इस प्रश्न या उत्तर में कोई त्रुटि है?
अध्याय 12: Organic Chemistry Some Basic Principles and Techniques - Multiple Choice Questions (Type - I) [पृष्ठ १५१]

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एनसीईआरटी एक्झांप्लर Chemistry [English] Class 11
अध्याय 12 Organic Chemistry Some Basic Principles and Techniques
Multiple Choice Questions (Type - I) | Q 36 | पृष्ठ १५१

संबंधित प्रश्न

Draw the resonance structure for the following compound. Show the electron shift using curved-arrow notation.

C6H5OH 


Draw the resonance structure for the following compound. Show the electron shift using curved-arrow notation.

C6H5NO2 


Draw the resonance structure for the following compound. Show the electron shift using curved-arrow notation.

CH3CH = CHCHO


Draw the resonance structure for the following compound. Show the electron shift using curved-arrow notation.

C6H5 – CHO


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’?

(A)
(i)
(ii)
(iii)
(iv)

What is the hybridisation of each carbon in H2C = C = CH2.


Show the polarisation of carbon-magnesium bond in the following structure.

CH3 – CH2 – CH2 – CH2 – Mg – X


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.


Draw the resonance structure of the following compounds;


Draw the resonance structure of the following compounds;

CH2 = CH – CH = CH2


Draw the resonance structure of the following compounds;

\[\begin{array}{cc}
\ce{CH2 = CH - C = O}\\
\phantom{.........}|\\
\phantom{.........}\ce{H}
\end{array}\]


Which of the following compounds will not exist as resonance hybrid. Give reason for your answer:


Resonance structures of propenal are given below. Which of these resonating structures is more stable? Give reason for your answer.

\[\ce{\underset{I}{CH2 = CH - CH = O} <-> \underset{II}{\overset{⊕}{C}H2 - CH = CH - \overset{Θ}{O}}}\]


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