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
Homework Answers
Add Answer to:
Which of the following reactions would you use to prepare
toluene from benzene?
Select one:
a....
- 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
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...
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...
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...
N III IV V 4. Everyone must write and post the reactions of benzene (chlorination, bromination, nitration, sulfonati...
N III IV V 4. Everyone must write and post the reactions of benzene (chlorination, bromination, nitration, sulfonation, Friedel Crafts Alkylation and Acylation) I= 1 1 1 ires Cyclize 2 not planar, 3) Cong xe) allcarn attalno b) xes spe Yes enta. 4 4 obey the so this not aromate Y > n. 2 some say not
1. What is the IUPAC name for the following compound? N 2. Which one of the...
1. What is the IUPAC name for the following compound? N 2. Which one of the following compound is aromatic? 3. Which one of the following compound is nonaromatic? IV 4Everyone must write and post the reactions of benzene (chlorination, bromination nitration, sulfonation, Fredel Crafts Alkylation and Acylation)
6. Which of the following reagents can be used to complete the reaction shown below? CH,CH,...
6. Which of the following reagents can be used to complete the reaction shown below? CH,CH, CH2-CECH CH,CHCHECH b. H2O with H2SO/HgSo. a. BH, followed by H2O2 d. None of the above. c. O, in CH,COOH 7. Which of the following is the major product of the reaction shown below? pyridine 8. Which of the following aromatic substitution reactions is most likely to give a polysubstituted product with benzene as a reactant? a. Friedel-Crafts Acylation b. Friedel-Crafts Alkylation c. Nitration...
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...
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...
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...
N III IV V 4. Everyone must write and post the reactions of benzene (chlorination, bromination, nitration, sulfonation, Friedel Crafts Alkylation and Acylation) I= 1 1 1 ires Cyclize 2 not planar, 3) Cong xe) allcarn attalno b) xes spe Yes enta. 4 4 obey the so this not aromate Y > n. 2 some say not
1. What is the IUPAC name for the following compound? N 2. Which one of the following compound is aromatic? 3. Which one of the following compound is nonaromatic? IV 4Everyone must write and post the reactions of benzene (chlorination, bromination nitration, sulfonation, Fredel Crafts Alkylation and Acylation)
6. Which of the following reagents can be used to complete the reaction shown below? CH,CH, CH2-CECH CH,CHCHECH b. H2O with H2SO/HgSo. a. BH, followed by H2O2 d. None of the above. c. O, in CH,COOH 7. Which of the following is the major product of the reaction shown below? pyridine 8. Which of the following aromatic substitution reactions is most likely to give a polysubstituted product with benzene as a reactant? a. Friedel-Crafts Acylation b. Friedel-Crafts Alkylation c. Nitration...
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