chlorine shows exceptionally higher electron gain enthalpy than that of florine.
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 ?”
It is the reaction between alkyl halides and sodium in the dry ether to give alkanes with higher number of carbon. 2R-X + 2 Na —> R-R +2NaX