Ortho and para nitrophenols are more aci | Class 12 Chemistry Chapter Alcohols Phenols and Ethers, Alcohols Phenols and Ethers NCERT Solutions

Welcome to the NCERT Solutions for Class 12 Chemistry - Chapter Alcohols Phenols and Ethers. This page offers a step-by-step solution to the specific question from Exercise 1, Question 8: . With detailed answers and explanations for each chapter, students can strengthen their understanding and prepare confidently for exams. Ideal for CBSE and other board students, this resource will simplify your study experience.

Question 8:

Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.

Answer:

Resonance structure of the phenoxide ion

Resonance structures of p-nitrophenoxide ion

Resonance structures of o-nitrophenoxide ion

It can be observed that the presence of nitro groups increases the stability of phenoxide ion.


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Comments

  • Lynn
  • Dec 16, 2019

why is it that in some books the resonance structures of o and p nitrophenol is given upto only the fifth resonating structure??


  • Sudhanshu
  • Nov 10, 2019

Para last structure is wrong correct it


  • Junaid sidiqui
  • Jul 24, 2018

In 5th resonating structure of p-isomer,double bonds should b b/w carbon no.2&3,4&5 but here double bonds are given b/w carbon no.1&2,4&5 which is not right.


  • Anish Modi
  • Jun 19, 2018

How can oxygen have 3 lone pairs.


  • SATVIR SINGH
  • Mar 15, 2017

Yes you are right the last structure will not have a double bond with oxygen atom.only a single bond will be their in the last structure because the electron involved in making double bond between carbon and oxygen has been transferred to the oxygen atom


  • Devesh
  • Mar 12, 2017

The structure of para is wrong as in the last step the topmost carbon is having 5 bonds which is not possible.


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Welcome to the NCERT Solutions for Class 12 Chemistry - Chapter . This page offers a step-by-step solution to the specific question from Excercise 1 , Question 8: Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corres....