Could I kindly ask you guys to help me out on question 1D) please !

c) This part involves compounds (5-8). NO2 CH3 (5) (6) (7) (8) i) Predict the major product obtained from the electrophilic bromination of compounds (5-8), briefly justifying your answers. ii) Place compounds (5-8) in order of their relative rate of reaction for bromination. iii) Draw a curly arrow mechanism to show the bromination of compound (6). [10 marks] d) Consider the following diazotisation reaction sequence. OH Br NH2 NaNO2, HCI Br NEN A 0 C, H20 i) Draw a curly arrow mechanism to show the formation of the diazonium salt (9). ii) Suggest a structure for compound A. [6 marks] e) Draw the product that results from the nucleophilic addition of the cyanide anion ("CN) to the 'lower' face of ketone (10). How does the hybridisation of the central carbon atom change during the reaction? H3C., C3H7 (10) [3 marks]