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Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions:...
Which of the following reactions would you use to prepare toluene from benzene? Select one: a....
Which of the following reactions would you use to prepare toluene from benzene? Select one: a. Friedel-Crafts Acylation reaction b. Halogenation c. Friedel-Crafts Alkylation reaction d. Nitration
using any of the starting material from the previous table, create a mechanism for the following...
using any of the starting material from the previous
table, create a mechanism for the following reactions
Use this table to answer the following questions in this week's exercise Complex Benzene Reactions Using any of the starting material from the previous table, create a mechanism for the following reactions: Redox reagents Starting compounds Common reactions H Pd-C, Fe HCI, ar Sn HC 2n(Hg)-HCI- NH NH OH- KMnD Na:Cr O: +H,SO, HO Nitration Benzene Sulfonation Toluene 1) Friedel-Crafts acylation of benzene...
Which one if the following reactions is most likely to give a polysubstituted product? Also i need help on question 2...
Which one if the following reactions is most likely to give a
polysubstituted product? Also i need help on question 29. Thank you
28. Which one of the following reactions is most likely to give a polysubstituted product? A) Friedel-Crafts alkylation B) Friedel-Crafts acylation C) Nitration D) Sulfonation E) Halogenation 29. Predict the major product for the following reaction. AlCl3
- Give the name of the product that results after the following two reactions are completed...
- Give the name of the product that results after the following two reactions are completed on benzene (use o-, m-, p- nomenclature): 1. Mix with a mixture of nitric and sulfuric acids 2. Mix with bromine in the presence of iron tribromide - Which of the following reactions would you use to prepare toluene from benzene? Select one: a. Nitration b. Friedel-Crafts Alkylation reaction c. Friedel-Crafts Acylation reaction d. Halogenation
solve the following: Use this table to answer the following questions in this week's exercise. Starting compounds Comm...
solve the following:
Use this table to answer the following questions in this week's exercise. Starting compounds Common reactions Nitration Benzene Toluene Sulfonation Redox reagents H2+ Pd-C, Fe+ HCl, or Sn+ HCI Zn(Hg) +HCl +4, NHANH + OH +4 KMnO4 Na2Cr207 +H2SO4+H2O Halogenation ZnO +4 Friedel-Crafts alkylation Friedel-Crafts acylation NBS - hy 8) Make p-nitrobenzoic acid using the previous table. 9) Make m-chlorethylbenzene using the previous table. How are you able to get the two groups in the meta position...
use this table to answer the following questions. Use this table to answer the following questions...
use this table to answer the following questions.
Use this table to answer the following questions in this week's exercise. Starting compounds Benzene Common reactions Nitration Toluene Sulfonation Redox reagents H2+ Pd-C, Fe+ HCl, or Sn+ HCI Zn(Hg) +HCI+, NH NH3 + 3H + KIMnO4, Na Cr 0; +H SO + H2O ZnO +1 Halogenation Friedel-Crafts alkylation Friedel-Crafts acylation NBS + hv Examples: This question is from the homework. What reaction(s)/reagent(s) do we use to prepare the prod What is...
8. All of the C-C bonds of benzene are: a. the same length b. radical like...
8. All of the C-C bonds of benzene are: a. the same length b. radical like in nature c. easy to break homolytically b. polyalkylation d. None of the above c. casy to break hetcrolytically 9. A limitation of the Friedel-Crafts acylation is: a. carbocation rearrangement c. reaction fails with very strong deactivators 10. Generally, the reaction with benzene with a halogen needsa as a promoter. a. Lewis base to serve b. Lewis acid c. Bronsted base d. Bronsted acid...
Starting with benzene as your only source of aromatic compounds, how would you synthesize the following...
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
c, d and e please c) You need to synthesize hexanedial which could be easily produced...
c, d and e please
c) You need to synthesize hexanedial which could be easily produced from oxidation of alkene. Using ozone oxidation, experiment with both dode-6-ene (C12H2a) and cyclohexene as starting material in separate reaction, then determine the most suitable starting material to obtain the desired product. Justify your answer with complete chemical reaction (6 marks) d) Illustrate reaction mechanism to produce 3-methylpentan-3-ol from butan-2-one using Grignard reagent: CH CH MgBr. (4 marks) e) Suppose a chemist needed to...
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
using any of the starting material from the previous
table, create a mechanism for the following reactions
Use this table to answer the following questions in this week's exercise Complex Benzene Reactions Using any of the starting material from the previous table, create a mechanism for the following reactions: Redox reagents Starting compounds Common reactions H Pd-C, Fe HCI, ar Sn HC 2n(Hg)-HCI- NH NH OH- KMnD Na:Cr O: +H,SO, HO Nitration Benzene Sulfonation Toluene 1) Friedel-Crafts acylation of benzene...
Which one if the following reactions is most likely to give a
polysubstituted product? Also i need help on question 29. Thank you
28. Which one of the following reactions is most likely to give a polysubstituted product? A) Friedel-Crafts alkylation B) Friedel-Crafts acylation C) Nitration D) Sulfonation E) Halogenation 29. Predict the major product for the following reaction. AlCl3
solve the following:
Use this table to answer the following questions in this week's exercise. Starting compounds Common reactions Nitration Benzene Toluene Sulfonation Redox reagents H2+ Pd-C, Fe+ HCl, or Sn+ HCI Zn(Hg) +HCl +4, NHANH + OH +4 KMnO4 Na2Cr207 +H2SO4+H2O Halogenation ZnO +4 Friedel-Crafts alkylation Friedel-Crafts acylation NBS - hy 8) Make p-nitrobenzoic acid using the previous table. 9) Make m-chlorethylbenzene using the previous table. How are you able to get the two groups in the meta position...
use this table to answer the following questions.
Use this table to answer the following questions in this week's exercise. Starting compounds Benzene Common reactions Nitration Toluene Sulfonation Redox reagents H2+ Pd-C, Fe+ HCl, or Sn+ HCI Zn(Hg) +HCI+, NH NH3 + 3H + KIMnO4, Na Cr 0; +H SO + H2O ZnO +1 Halogenation Friedel-Crafts alkylation Friedel-Crafts acylation NBS + hv Examples: This question is from the homework. What reaction(s)/reagent(s) do we use to prepare the prod What is...
8. All of the C-C bonds of benzene are: a. the same length b. radical like in nature c. easy to break homolytically b. polyalkylation d. None of the above c. casy to break hetcrolytically 9. A limitation of the Friedel-Crafts acylation is: a. carbocation rearrangement c. reaction fails with very strong deactivators 10. Generally, the reaction with benzene with a halogen needsa as a promoter. a. Lewis base to serve b. Lewis acid c. Bronsted base d. Bronsted acid...
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
c, d and e please
c) You need to synthesize hexanedial which could be easily produced from oxidation of alkene. Using ozone oxidation, experiment with both dode-6-ene (C12H2a) and cyclohexene as starting material in separate reaction, then determine the most suitable starting material to obtain the desired product. Justify your answer with complete chemical reaction (6 marks) d) Illustrate reaction mechanism to produce 3-methylpentan-3-ol from butan-2-one using Grignard reagent: CH CH MgBr. (4 marks) e) Suppose a chemist needed to...
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