6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis...

Question

Question

Answer 1

Answer #1

The answer is given in the attachment.

H3C CI O conc. HNO3 conc. H2SO4 AICI: Friedel-Craft acylation Hg2+ Non aqueous medium Product CH 7) Bry/FeBrz H₂C a on AICI:

Answer 2

Similar Homework Help Questions

Starting with Benzene and using any other necessary reagents of your choice a synthesis for the...

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 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 (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) रेर Br (i) Н-N. Br NH2 (k) Br "SoH
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

Starting with benzene and using any other neccessary reagents of your choice, design a synthesis for...

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
6. Design a synthesis of the following compound starting from benzene and any other organics and...

6. Design a synthesis of the following compound starting from benzene and any other organics and inorganics (12 pts) OH 6. Design a synthesis of the following compound starting from benzene and any other organics and inorganics (12 pts) OH
20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis...

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

Practice Problem 23.50 Starting with cyclopentene and using any other reagents of your choice, show how...

Practice Problem 23.50 Starting with cyclopentene and using any other reagents of your choice, show how you would make each of the following compounds: (a) (b) (c) HO OH Choose from the following list of reagents: c b d Pd[OAC)2, PPhy, BN NaOH, H20, heat H,0NaOH (xs) CH2CH2 f g e BHy-THF (xs) CHşlyZn-Cu. Et, BCOM) h Grubbs catalyst i k - BE Be Using the reagents above, list in order (by letter, no period) those necessary to provide each...
1. Starting with benzene and any necessary reagents, design an efficient synthesis of the following compound:...

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
1 synthesis for each of the following compounds. Some problems have more than one plausible Starting...

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...

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