20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3 20. (8 pts)...
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
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
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
Provide a reasonable multistep synthesis of the following
molecule from the indicated starting material, using any reagents
necessary. (Please include the product and reagents of each
individual step in your synthesis.
DER
just need wuestion 20 completed all work
20 Starting from benzene or anisole and any other reagent of your choice, design a synthesis for cach of the following compounds. (18 pts) осн. OCH Q --C 21. Predict the products from the Birch reductions shown below. (3 pts) Na, NH C,OH Bonus: (6 pts) Provide a synths for the target molecule using benzene. сон 1 1
Bonus: Provide a synthesis for the target molecule starting from Benzene (5 pts).
Bonus: Provide a synthesis for the target molecule starting from Benzene (5 pts).
Complete the reactions to show the synthesis of the following compound from cyclohexene as the starting material.
Provide the reagent(s) necessary to complete the following
synthesis.
I Bra
. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) Retrosynthesis HO O 04
2. Propose an elegant synthesis of the following molecule starting from terminal alkyne compounds of five carbons or fewer as your only source of carbon. You may use any other reagent necessary. CH3 CH3 H3C CH3