(Solved): help please with the chooses, note:all the queatios has the same chooses The incomplete mechanism fo ...

The incomplete mechanism for the formation of acetylferrocene is shown below. Complete the following statements which relate to where the curly arrows would need to be drawn to complete the mechanism: N. B. in the reaction scheme, numbers in bold refer to atoms whereas numbers in red are bonds. If this causes problems (due to visual impairment for example), please contact me (r.mewis@mmu.ac.uk) for help. STAGE 1 which means it is electron \( \mathrm{AlCl}_{y} \) is used in this reaction as a \( \mathrm{AlCl}_{3} \) is used in this reaction as a which means it is electron A lone pair of electrons from the atom of \( \mathrm{AlCl}_{3} \) STAGE 1 \( \mathrm{AlCl}_{3} \) is used in this reaction as a which means it is electron \( \mathrm{AlCl}_{3} \) is used in this reaction as a A lone pair of electr STAGE 2 The charge from the oxygen is moved from (bond or atom) to reform the bond. Subsequently, the bond linking atoms 3 and is broken to release \( \mathrm{AlCl}_{4} \) - The aromaticitv of the cyclopentadienyl ring is restored by moving the pair of electrons in bond in to the aromatic ring - the aromatic ring is labelled in the reaction scheme. As well as the desired product, \( \mathrm{HCl} \) and \( \mathrm{AlCl}_{3} \) are formed. The latter is necessary as this is a for the reaction and therefore can be involved in a further substitution between ferrocene and acetyl chloride. The reaction depicted is an example of a Friedel-Crafts acylation reaction.