1- Which of the phenol and p-nitrophenol compounds is more acidic?
Explain by drawing the resonance structures of conjugate bases.
2- Write the products of the cis-1-chloro-3-ethyl cyclohexone compound with methanol under the reaction conditions of SN1 and E1 by its mechanism.
3- Design a synthesis scheme for 1- (p-methylphenyl) -2-methyl-1,3-butanedione using the compound of the active metal as the starting compound and other reagents that may be required.
The para is more acidic.
Can't draw structures on this forum.