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QUESTION 1 Which of the following compounds could be made most easily in one step from...
Organic Chemistry 2 STION 1 Nhich of the following compounds could be made most easily in...
Organic Chemistry 2
STION 1 Nhich of the following compounds could be made most easily in one step from benzene using a Friedel-Crafts reaction? Which would be the best reagent for carrying out the reaction shown below? TN- АН,0 в Н,РО, С н,РО, DH,SO, JESTION 3 Which of the compounds shown below would be the major organic product of the set of reactions shown? HNO3 H2SO4 Pd /C NaNO2 HCI 0° NH SH WEN
1. From what diene and dienophile could each of the following be made? (2 pts. each)...
1. From what diene and dienophile could each of the following be made? (2 pts. each) -NO₂ NO2 2. Starting from benzene, propose a step-by-step reaction sequence that would produce the following molecule (8 pts.) NO2 OH 3. What combination of acid chloride and arene would you chose to prepare each of the following compounds by Friedel-Crafts acylation? (2 pt. each)
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...
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
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
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 statements are TRUE about the retrosynthesis of the molecule below. Choose the answer option that...
Which statements are TRUE about the retrosynthesis of the molecule below. Choose the answer option that statements. A. The molecule can be made in one step using Friedel Crafts Alkylation B. The molecule can be made in one step using Friedel Crafts Acylation C. The molecule could be prepared using a Grignard reagent and CO2 D. The molecule could be prepared from a nitrile E. The molecule cannot be prepared from acetylene F. The molecule could be prepared from oxidation...
- 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...
Question 4 (10 pts) Each of the following compounds can be made with a Friedel-Crafts acylation....
Question 4 (10 pts) Each of the following compounds can be made with a Friedel-Crafts acylation. Identify the acyl chloride and the aromatic compound you would use to produce each compound. EXPLAIN YOUR CHOICES ON. yola OCH3 OCH3 H3CO
Organic Chemistry 2
STION 1 Nhich of the following compounds could be made most easily in one step from benzene using a Friedel-Crafts reaction? Which would be the best reagent for carrying out the reaction shown below? TN- АН,0 в Н,РО, С н,РО, DH,SO, JESTION 3 Which of the compounds shown below would be the major organic product of the set of reactions shown? HNO3 H2SO4 Pd /C NaNO2 HCI 0° NH SH WEN
1. From what diene and dienophile could each of the following be made? (2 pts. each) -NO₂ NO2 2. Starting from benzene, propose a step-by-step reaction sequence that would produce the following molecule (8 pts.) NO2 OH 3. What combination of acid chloride and arene would you chose to prepare each of the following compounds by Friedel-Crafts acylation? (2 pt. each)
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...
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
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 statements are TRUE about the retrosynthesis of the molecule below. Choose the answer option that statements. A. The molecule can be made in one step using Friedel Crafts Alkylation B. The molecule can be made in one step using Friedel Crafts Acylation C. The molecule could be prepared using a Grignard reagent and CO2 D. The molecule could be prepared from a nitrile E. The molecule cannot be prepared from acetylene F. The molecule could be prepared from oxidation...
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...
Question 4 (10 pts) Each of the following compounds can be made with a Friedel-Crafts acylation. Identify the acyl chloride and the aromatic compound you would use to produce each compound. EXPLAIN YOUR CHOICES ON. yola OCH3 OCH3 H3CO
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