Show how you would synthesize 4-bromo-2-nitrotoluene from benzene.
Starting with benzene as your only source of aromatic compounds, how would you synthesize the following substances? Assume that you can separate ortho and para isomers if necessary. p-Chlorotoluene m-Bromonitrobenzene o-Bromobenzenesulfonic acid m-Chlorobenzenesulfonic acid Starting with either benzene, phenol, or toluene, how would you synthesize the following substances? Assume that ortho and para isomers can be separated 2-Bromo-4-methylphenol 1,3,5-Trinitrobenzene 2,4,6-Tribromoaniline 2-Chloro-4-nitrotoluene
sbow how you woukd synthesize each of the following compounds from benzene (a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
Show how you can synthesize the compound from a benzene Show how you can synthesize the compound from benerene COOH - Br NH2
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You may use any other reagent necessary
h. and i. Starting with benzene how would you synthesize j.+k. Starting with benzene how would you synthesize I. and m. HAC -NH trace H,00 + H2O CHE o. and p. HẠN H30 NHA KOH/H, - H2O Heat 1) LAH R' 2) H20 H20 Heat t. and u. 1)H,0* HS 2) Raney Ni
0.5 pts Question 4 (10 points) Show how you would synthesize the following aromatic compound from benzene and any other reacents necessary. Hint: Retrosynthesis. P .NO2 u h CH3 The reaction code in the box is:
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
17-52 Show how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclic reagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures. 1-phenyl-1-bromobutane 1-phenyl-1-methoxybutane 3-phenylpropan-1-ol ethoxybenzene 1,2-dichloro-4-nitrobenzene 1-phenylpropan-2-ol p-aminobenzoic acid 2-methyl-1-phenylbutan-2-ol 5-chloro-2-methylaniline 3-nitro-4-bromobenzoic acid 3-nitro-5-bromobenzoic acid 4-butylphenol 2-(4-methylphenyl)butan-2-ol
Starting with benzene, how would you synthesize the following products? You can use any chemical you can find from chapter 7- 13, or 16-18 to help you in your synthesis. (15 pts, 5 points each) 3. Starting with benzene, how would you synthesize the following products? You can use any chemical you can find from chapter 7-13, or 16-18 to help you in your synthesis. (15 pts, 5 points each) OH o-bo
1) Show how you might synthesize m-bromobenzoic acid, using benzene and any suitable catalyst as your starting materials. 2) Show how you might synthesize 2-methylhexane, using acetylene and any suitable alkyl halides as your starting materials.