Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

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Determine the appropriate order of basicity.

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Important Questions on Principles of Organic Chemistry

EASY

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

Among the following oxoacids, the correct decreasing order of acid strength is :

HARD

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct order of acidity for the following compounds is :
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EASY

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct increasing order of the basic strength for the following compounds is:

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EASY

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The

N

which contribute least to the basicity of the compound is :
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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct order for acid strength of compounds

CH \equiv CH, {CH}_{3} - C \equiv CH

and

{CH}_{2} = {CH}_{2}

is as follows:

HARD

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The increasing order of basicity of the following compounds is :
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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The compound that does NOT liberate CO₂, on treatment with aqueous sodium bicarbonate solution, is

HARD

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

An organic compound

‘ X ’

showing the following solubility profile is:
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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct statement regarding the basicity of aryl amines is:

HARD

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct order of strengths of carboxylic acids is

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HARD

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

What is the order of basicity among the following compounds?

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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The increasing basicity order of the following compounds is:

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HARD

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The increasing order of the

{p K}_{b}

of the following compund is:

(A)

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(B)

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(C)

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(D)

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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

Considering the basic strength of amines in an aqueous solution, which one has the smallest

{pK}_{b}

value?

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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct order of the basis strength of methyl substituted amines in aqueous solution is:

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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The increasing order of

p K_{b}

for the following compounds will be :
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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

In the following compounds, the decreasing order of basic strength will be:

EASY

Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

In case of substituted aniline the group which decreases the basic strength is

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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

Among the following, which is least acidic?

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Chemistry>Organic Chemistry>Principles of Organic Chemistry>Resonance Effects

The correct order of basicity is