Propose routes to the following compounds from propyl bromide and any necessary organic or inorganic reagents:
Propose routes to the following compounds from propyl bromide and any necessary organic or inorganic reagents:...
(4pts) Propose a synthetic scheme from benzene and any other organic or inorganic reagents for the following compounds. a. COOH ci SOH NH2
Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organic reagent of TWO carbons or less: 4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
Page 4 Propose reasonable syntheses for the following compo compounds and using any other necessary organic intermediates formed to receive full credit. Assume separated. ng compounds beginning with the indicated organic or inorganic reagents. Show all sume any isomers formed can easily be [3% +6% marks] c. Provide any required reagents and give the stru following synthetic scheme. If more than one reaga steps. ve the structures of the intermediates in the one reagent is required, please number the Bra,...
1. Give the organic 2. Propose a synthetic routes for the following chemical transformation. You may use any organic or inorganic reagents we have discussed in class. You may need to use reactions from CHEM 371. products of the following reactions
19. Complete the following synthesis using any inorganic or organic compounds necessary. You must show all reagents, solvents, and intermediate products for full credit. (10 pts) OH OCH3
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and any inorganic compounds. Include all mechanisms, steps, reagents, and reactions used. СН3 NH2 СН3
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and any inorganic compounds. Include all mechanisms, steps, reagents, and reactions used. CH3 NH2 СН3
1. Propose synthetic routes to prepare the compounds from the shown starting materials in 2 steps. Use any reagents as necessary: OH U from OH
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents (14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
u.Propose a synthesis of the following molecule from benzene and any organic or (" inorganic reagents necessary. In your synthesis, you can only separate isomers in the middle of the synthesis, the final step should give only the desired product. (Hint! Don't forget about carbocation rearrangements.)