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- Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Draw all the oissuvke resonance forms of methoxybenzene, including the hybrid Based on the structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.Predicts the major products for the following reaction.Complete the Reaction below and provide the following (i) a detailed stepwise mechanism to account for the product(s), including all steps involved (ii) Clearly show all the resonance structures and intermediates formed leading to the product. OH acetic anhydride
- (b) Propose a mechanism for the following reaction, with curved arrows to show bonding changes. OH H2SO4 + THF HO HOQ.6 Suggest a plausible mechanism for the following transformation Ph Ph BuzSnH AIBN SMeShow how the following ketones might be synthesized from the indicated acids, usingany necessary reagents.(b) methyl cyclohexyl ketone from cyclohexanecarboxylic acid