What is the major product from a reaction of nitrobenzene with Fe/HCL?
How would you synthesize 3-chlorobenzoic acid, starting with benzene?
What is the major product from a reaction of nitrobenzene with Fe/HCL? How would you synthesize...
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
1. Predict the major products formed when benzene reacts with the following reagents. (a). tert-butyl bromide, ALCl3 (b) bromine + a nail (c) iodine + HNO3 (d) carbon monoxide, HCl, and AlCl3/CuCl (e) nitric acid + sulfuric acid. 2. Predict the major products of the following reactions. (a.) nitrobenzene + ethyl chloride/AlCl3 (b). p-methylanisole + acetyl chloride + AlCl3 (c). nitrobenzene + fuming sulfuric acid (d) benzene + CH3CH2COCl in the presence of (1) ALCl3 followed by...
what is the major product in the following reaction? which reaction sequence would accomplish this transformation? What is the major product in the following reaction? 1. CHyl (excess) NH 2. Ag2O, H2O, heat HN Which reaction sequence would accomplish this transformation? yogh Н 1. H30+, CH2OH 2. NaBH, 3. H20+ O 1. p-TsOH, HOCH,CH,OH 2. NaBH4 3. H30+ 01. pTsOH, HOCH,CH,OH 2. CH3MgBr 3. H307 O 1. CH_MgBr 2. H3O+ 3. CH3OH What is the best starting material to synthesize...
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
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You may use any other reagent necessary
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
3.) For each of the following compounds, draw the major organic product of reaction with HCl or NaOH and circle whether the starting materials and products will be more soluble in organic solvent or water Benzoic Acid + HCl: Benzoic Acid + NaOH: OH Benzoic Acid Water/Organic Water Organic Fluorenone HС: Fluorenone + NaOH: Fluorenone Water/Organic Water/Organic Веnzocaine + HCi: Benzocaine + N»OH: H2N Benzocaine Water/Organic Water Organic O= 3.) For each of the following compounds, draw the major organic...
could someone please answer these 3 questions? 2. What product would you expect from the following reaction? ÇOCH B ÇOCH A oi CO2CH3 B ÇOCH E. CO2CH3 4. What will be the best way to synthesize the following compound starting from benzene? D CO2CH3 8 E A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI; 2) Zn, HCI; 3) Cl2, FeCls;...
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
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...