To answer this we have to see the reactive nature of phenol and the substituents attached to it. Acidic behavior of phenol depends on the fact that how easily it can loose a proton and make phenoxide ion which is stabilized by resonance. The methoxy group being electron donating group increases the electron density ofContinue reading “Why ortho-nitrophenol is more acidic than ortho-methoxy phenol ?”
Tag Archives: ortho
What are the chemical properties of Carboxylic Acids ?
Why CH3 group is Ortho and para directing in nature in Toulene ?
IN CASE OF TOLUENE the methyl group attached to the ring, increases the electron density at ortho and para positions by resonance without changing anything at the meta position. Thus the attacking reagent directly attacks at the electron rich site , thus the methyl group is ortho directing. you can easily understand the movement ofContinue reading “Why CH3 group is Ortho and para directing in nature in Toulene ?”
Which is more acidic ortho methyl phenol or phenol?
the phenol is more acidic as compared to ortho methyl phenol because the methyl group is electron releasing group which will increase the electron density in the ring as well as on the carbon atom attached to -OH (hydroxyl group) thus -OH group will not release the H+ ion. but in case of phenol thereContinue reading “Which is more acidic ortho methyl phenol or phenol?”