all 3 please! thank you!!!!

Which of these structures would be the most stable contributor to the resonance hybrid formed when anisole undergoes nitration? How does anisole direct? Does anisole activate or deactivate the ring for EAS reactions? A B C D E For each EAS reagent shown on the left, choose the correct base to deprotonate and restore aromaticity to the ring in step 3 of the mechanism. CH3CH2Cl,AlCl3 H2O Cl2,AlCl3 Which of the following is NOT a limitation of a Friedel-Crafts reaction. Alkyl halides must have the halogen attached to an sp3 hybridized carbon Friedel-Crafts acylation often leads to polyacylated products. Friedel-Crafts alkylation substrates can undergo rearrangement Friedel-Crafts alkylation often leads to polyalkylated products. Friedel-Crafts reactions can not be done on moderately or strongly deactivated ring systems