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Standard XIII

Chemistry

Acidity of Carboxylic Acids

Consider the ...

Question

Consider the acidity of carboxylic acids i.Ph - COOH ii. o - NO₂ C₆H₄COOH iii. p - NO₂ C₆H₄COOHiv. m - NO₂ C₆H₄COOH which of the following order is correct

i > ii > iii >iv

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ii >iv> iii > I

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ii >iv> I > iii

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ii > iii >iv> I

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Solution

The correct option is D ii > iii >iv> I
-NO₂ group is deactivator and increases acidic nature and in ortho&para position involved in resonance but not in meta position

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Similar questions

Q. Arrange the following in correct order of acidic strength.

(I)

C H_{3} N O_{2}

(II)

N O_{2} C H_{2} - N O_{2}

(III)

C H_{3} - C H_{2} - N O_{2}

(IV)

N O_{2} - C | H N O_{2} - N O_{2}

Q. Correct acidic strength of the following carboxylic acids:

C_{6} H_{5} C O O H

o - N O_{2} (C_{6} H_{4}) C O O H

p - N O_{2} (C_{6} H_{4}) C O O H

m - N O_{2} (C_{6} H_{4}) C O O H

Q. Consider the acidity of the carboxylic acids.
(i)

P h C O O H

(ii) o-

N O_{2} C_{6} H_{4} C O O H

(iii) p -

N O_{2} C_{6} H_{4} C O O H

(iv) m -

N O_{2} C_{6} H_{4} C O O H

which of the following order is correct ?

Consider the acidity of carboxylic acids i.Ph - COOH ii. o - NO₂ C₆H₄COOH iii. p - NO₂ C₆H₄COOHiv. m - NO₂ C₆H₄COOH which of the following order is correct

Q. Consider the acidity of the carboxylic acids:
(i)

C_{6} H_{5} C O O H

(ii)

O - N O_{2} C_{6} H_{4} C O O H

(iii)

p - N O_{2} C_{6} H_{4} C O O H

(iv)

m - N O_{2} C_{6} H_{4} C O O H

Which of the following order is correct?

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Consider the acidity of carboxylic acids i.Ph - COOH ii. o - NO2 C6H4COOH iii. p - NO2 C6H4COOHiv. m - NO2 C6H4COOH which of the following order is correct

The correct option is D ii > iii >iv> I-NO2 group is deactivator and increases acidic nature and in ortho&para position involved in resonance but not in meta position

Consider the acidity of carboxylic acids i.Ph - COOH ii. o - NO₂ C₆H₄COOH iii. p - NO₂ C₆H₄COOHiv. m - NO₂ C₆H₄COOH which of the following order is correct

The correct option is D ii > iii >iv> I
-NO₂ group is deactivator and increases acidic nature and in ortho&para position involved in resonance but not in meta position