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Consider the following reaction and answer the questions that follow: ia Meo Me AICI: CI Meo Me 7 8 (a) Using the templates provided below, draw the set of relevant resonance forms of the intermediate carbocation formed during this reaction, which is consistent with the outcome of the reaction. (4) (b) Another possible product of this reaction, structure 9, is shown below. Give a reason why this could in fact be a major product of the reaction, despite the addition happening at what seems to be the most hindered position of the benzene ring. (1) Meo Me (c) If the reaction is repeated starting with compound 10, as shown below, product 11 is formed: AICI ON Me ON Me 10 11 (l) State whether this overall reaction is faster or slower than the first reaction above (which starts with 7), and give a reason for your answer. (2) (II) Explain, using structures of relevant intermediates, why the product 12 shown below would not be expected to form in this case. (2) O2N Me 12