Starting from benzene and using any other necessary reagents of your choice, design a synthesis for...
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1 answer (a) Cl. .NO2 (b) НAN. (c) H2N (d) (e) Br СООН СООН Br (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) Br H2N Br Cl -NH2 Cl (k) Br
6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 7. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 8. Starting with benene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there...
Starting with Benzene and using any other necessary reagents of your choice a synthesis for the following compound. Assume that ortho and para isomers can be There may be more than one plausible answer.
Starting with benzene and using any other neccessary reagents of your choice, design a synthesis for each of the following: OMe COOH Br Br NO NO (b) COOH NH Cl Cl NO2 COOH NO2 Cl NO Cl Br OEt NO2 Cl (h) C (g) NO2 Br O2N
1 synthesis for each of the following compounds. Some problems have more than one plausible Starting from benzene and using any other necessary reagents of your choice, design a answer (a) NO2 (b) Н-N, (c) Н.N. (d) (e) Br COOH (f COOH
20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis for each of the following compounds. (18 pts) OCH
20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis for each of the following compounds. (18 pts) 21. Predict the products from the Birch reductions shown below. (3 pts) Na GLO Bonus: (6 pts) Provide a synthesis for the target molecule using benzene. COH COH TM
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
please show work 20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis for each of the following compounds. (18 pts) TO ) сон CBry
1. Starting with benzene and any necessary reagents, design an efficient synthesis of the following compound: 1. Provide a detailed curved-arrow mechanism to account for the transformation below and explain why the only products formed at high and low temperatures are the ones shown. (Show all resonance contributors for all intermediates): HCl, Clos Cocha осн