why para nitrophenol is more acidic than phenol explain with resonance structure?

why para nitrophenol is more acidic than phenol explain with resonance structure?
Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of corresponding phenoxide ions. The electron withdrawing groups are more effective in increasing the acidic strength at the para-position relative to the ortho position because of greater dispersal of charge on oxygen atom.
Full answer in: www.zigya.com
Why para nitrophenol is more acidic than phenol explain with resonance structure?
Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of corresponding phenoxide ions. The electron withdrawing groups are more effective in increasing the acidic strength at the para -position relative to the ortho position because of greater dispersal of charge on oxygen atom.
Full answer in: www.zigya.com
Which of the two phenol or o nitrophenol are more acidic and why?
As a result, it is easier to lose a proton. Also, the o -nitrophenoxide or p-nitrophenoxide ion formed after the loss of protons is stabilized by resonance. Hence, ortho and para nitrophenols are stronger acids than phenol. Feb 19, 2013
Full answer in: www.topperlearning.com
Why is para nitrophenol more acidic than phenol?
The p - nitrophenol is more acidic than phenol because the deactivating nature of nitro group and after loosing the protons it makes more resonance stabilization as nitro group is having strong deactivating nature so it attracts electrons towards it. Apr 14, 2020
Full answer in: www.careers360.com