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Define permanent electronic effects.

Important Questions on Organic Chemistry: Some Basic Principles and Techniques

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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects

Increasing order of stability of the resonance structure is:

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Which one among the following resonating structures is not correct?
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Draw the resonating structures of Aniline.
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to 
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Resonance effect is not observed in
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
In pyrrole, the electron density is maximum on

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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Draw the resonating structures of Urea.
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Which of the following is correct with respect to -I effect of the substituent? (R=alkyl group)
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects

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

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respectively, are

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The chlorine atom of the following compound

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that reacts most readily with AgNO3 to give a precipitate is

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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
A tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following?
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Which of the following molecules is least resonance stabilized?
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Which of the following represents the hyperconjugation effect?
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Consider the following compounds

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Hyperconjugation occurs in:
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
The higher stabilities of tert-butyl cation over isopropyl cation and trans-2- butene over propene, respectively, are due to orbital interactions involving
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
Identify the functional group that has electron donating inductive effect.
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Which of the following carbocations is expected to be the most stable?
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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects

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Among the given species the Resonance stabilised carbocations are:

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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
The correct order of stability for the following alkoxides is:

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Chemistry>Organic Chemistry>Organic Chemistry: Some Basic Principles and Techniques>Electronic Effects
In which of the following molecules, all atoms are coplanar?