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Draw a reasonable mechanism for the given reaction
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- Provide reagentsProvide the starting materials needed to prepare the following compounds:1. At what position and on what ring would you expect the following substances to undergo electrophilic substitution? (b) CH3 Br lel CH3 2. Rank the compounds in each group according to their reactivity toward electrophilic substitution. (a) Chlorobenzene, o-dichlorobenzene, benzene (b) p-Bromonitrobenzene, nitrobenzene, phenol (c) Fluorobenzene, benzaldehyde, 0-xylene (d) Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrile
- Determine whether each of the following syntheses requires a reaction that alters the carbon skeleton. (a) (b) OH (c) (d) OCH,CH3 CH3 (e) OH (f) H,CO он H;CO. (g) H3CO, (h) H3CO. NO2 NO2Predicts the major products for the following reaction.D H,O* CH,CI H,SO, H3C KMNO, + + ΗΝO, H A AICI, AICI, A Cl, FeCl, F+ G 7. Based on the reaction scheme above: (a) Draw the structural formula for compound A to H. (b) Show the mechanism for the formation of compound C. (c) Explain why the activating group, such as -OH is ortho and para director. Give an example of a compound from the reaction scheme. (d) Explain why a deactivating group, such as -NO2 is a meta director. Give an example of compound from the reaction scheme. Br2 FeBr3
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