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Which of the following compound shows resonance?
(a)

(b)

(c)

(d)


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Important Questions on Organic Chemistry- Some Basic Principles and Techniques
EASY
The lower stability of ethyl anion compared to methyl anion and the higher stability of ethyl radical compared to methyl radical, respectively, are due to

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Which of the following is correct with respect to effect of the substituent? (alkyl group)

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Which of the following represents the hyperconjugation effect?

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The higher stabilities of tert-butyl cation over isopropyl cation and trans-- butene over propene, respectively, are due to orbital interactions involving

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Which of the following molecules is least resonance stabilized?

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The chlorine atom of the following compound
that reacts most readily with to give a precipitate is

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A tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following?

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In which of the following molecules, all atoms are coplanar?

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The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to

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Which of the following has the shortest bond?

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Which of the following carbocations is most stable?

EASY
Consider the following compounds

Hyperconjugation occurs in:

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Choose the correct statement regarding the formation of carbocations A and B given :-

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The most acidic proton and the strongest nucleophilic nitrogen in the following compound
respectively, are

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Identify the functional group that has electron donating inductive effect.

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Among the following compounds, which one has the shortest bond?

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The correct order of stability for the following alkoxides is:


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Resonance effect is not observed in

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In pyrrole, the electron density is maximum on


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Which of the following carbocations is expected to be the most stable?

