Arrange the following compounds in correct order of acidic strength.
A
HCOOH>CH3COOH>C6H5OH>C2H5−OH
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B
CH3COOH>HCOOH>C6H5OH>C2H5−OH
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C
C6H5OH>HCOOH>CH3COOH>C2H5−OH
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D
None of these
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Solution
The correct option is DHCOOH>CH3COOH>C6H5OH>C2H5−OH The correct increasing order of acidic strength is given by C2H5OH<C6H5OH<CH3CO2H<HCO2H. When substituent group is electron releasing, then the acidity decreases. Hence CH3CO2H is less acidic than HCO2H.
As both C2H5OH & C2H5OH come under alcohols C2H5OH is acidic acid due to resonance stabilized C6H5O− ion.