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Starting with benzene as your only source of aromatic compounds, how would you synthesize the following...
17-52 Show how you would synthesize the following compounds, starting with benzene or toluene and any...
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
Outline all steps in the laboratory synthesis of the following compounds from benzene and/or toluene, using...
Outline all steps in the laboratory synthesis of the following compounds from benzene and/or toluene, using any needed aliphatic or inorganic reagents. Assume the para isomer can be separated from an ortho,para mixture. Do not show mechanisms. p-bromobenzoic acid m-bromobenzoic acid 2-bromo-4-nitrotoluene 2-bromo-4-nitrobenzoic acid 4-bromo-3-nitrobenzoic acid o-iodobenzoic acid
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is...
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CH₂
Aromatic Synthesis Reactions Starting with benzene, propose syntheses to carry out each of the following conversions....
Aromatic Synthesis Reactions Starting with benzene, propose syntheses to carry out each of the following conversions. Assume ortho and para isomers can be separated.
Hello everyone, I'm having serious doubts about my answers for this activity and I need help....
Hello everyone, I'm having serious doubts about my
answers for this activity and I need help.
Instructions for this activity:
How would you synthesize the following substances
starting from benzene? Assume that ortho- and para- substitution
products
can be separated. Show all reactions.
My answers:
1 - 3
4 - 6
7 - 9
10
Your help will be much appreciated!
1. C-huelcony melly I heezerve OH 044 Freidel Crafts pikylation. CH₃ G Oxidation N20 + CH₂Cl AlCl₃ Benzene Phenol...
6). (10 points) Predict the mononitration products of the following compounds. a) o-nitrotoluene b) m-chlorotoluene c)...
6). (10 points) Predict the mononitration products of the following compounds. a) o-nitrotoluene b) m-chlorotoluene c) o-bromobenzoic acid d) p-methoxybenzoic acid e) m-cresol (m-methylphenol) (Two products) (Three products) (Two products) (One product) (Three products) 7). (12 points) Show how you would synthesize the following aromatic derivatives from benzene. You don't have to show mechanisms just show synthesis pathways. a) p-tert-butylnitrobenzene b) p-toluenesulfonic acid c) p-chlorotoluene glad noeg banorte
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and...
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
Show how you would synthesize 4-bromo-2-nitrotoluene from benzene.
Show how you would synthesize 4-bromo-2-nitrotoluene from benzene.
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions:...
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...
h. and i. Starting with benzene how would you synthesize j.+k. Starting with benzene how would...
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
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CH₂
Aromatic Synthesis Reactions Starting with benzene, propose syntheses to carry out each of the following conversions. Assume ortho and para isomers can be separated.
Hello everyone, I'm having serious doubts about my
answers for this activity and I need help.
Instructions for this activity:
How would you synthesize the following substances
starting from benzene? Assume that ortho- and para- substitution
products
can be separated. Show all reactions.
My answers:
1 - 3
4 - 6
7 - 9
10
Your help will be much appreciated!
1. C-huelcony melly I heezerve OH 044 Freidel Crafts pikylation. CH₃ G Oxidation N20 + CH₂Cl AlCl₃ Benzene Phenol...
6). (10 points) Predict the mononitration products of the following compounds. a) o-nitrotoluene b) m-chlorotoluene c) o-bromobenzoic acid d) p-methoxybenzoic acid e) m-cresol (m-methylphenol) (Two products) (Three products) (Two products) (One product) (Three products) 7). (12 points) Show how you would synthesize the following aromatic derivatives from benzene. You don't have to show mechanisms just show synthesis pathways. a) p-tert-butylnitrobenzene b) p-toluenesulfonic acid c) p-chlorotoluene glad noeg banorte
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
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...
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
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