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The ascending order of acidity of – OH group in the following compounds is : (A) Bu – OH Choose the correct answer from the options given below :

Options

  1. A( A ) < ( D ) < ( C ) < ( B ) < ( E )
  2. B( C ) < ( A ) < ( D ) < ( B ) < ( E )
  3. C( C ) < ( D ) < ( B ) < ( A ) < ( E )
  4. D( A ) < ( C ) < ( D ) < ( B ) < ( E )

Correct answer

D. ( A ) < ( C ) < ( D ) < ( B ) < ( E )

Step-by-step solution

The decrease in electron density of the O - H bond of o,p-dinitrophenol, the polarity of O - H bond decreases. The electron withdrawing group - NO 2 ), withdraws electrons and disperses the negative charge. Therefore, - NO 2 group stabilizes the phenoxide ion. Hence, o,p-dinitrophenol is more acidic than p-nitrophenol and phenol. OMe is an electron donating group, hence it increases electron density, there why making it less acidic. Bu - OH is an aliphatic alcohol. In phenoxide ion the negative charge is delocalize

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