Asked by Hiba
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.
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.
Answers
Answered by
DrBob222
The para is more acidic.
Can't draw structures on this forum.
Can't draw structures on this forum.
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