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10 Nov 2019

I have already proven the first part, number 16, but I can'tfigure out how to do the second part number 17. Help!

Genetic catalylic reaction. As also discussed in class, consider the following example of a S + C SC P + C with S for the substrate/reactant, C the catalyst, SC an intermediate, and P the reaction product. You could work on part 18 and 19 even if you could not solve sub-problems 16. Use the steady-state approximation for the intermediate and show that (15%)

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I have already proven the first part, number 16, but I can'tfigure out how to do the second part number 17. Help!

I need help with problem number 17. I've already solved number16, but I'm showing it in relation to the second problem.

1. Which of the following reagent(s) can be used to prepare a mixture of o and p-nitro toluene from toluene

(A) HNO₂ (B) HNO₃ (C) HNO₃/Fe (D) HNO₃/H₂SO₄ (E) NaNO₂

(A) H₂SO₃ (B) SO₃/ Which of the following reagent(s) can be used to convert nitrobenzene to m-nitrobenzenesulfonic acid Fe (C) H₂SO₃/Fe (D) H₂SO₄/Al₂(SO₄)₃ (E) H₂SO₄.SO₃

3. Which of the following reagent(s) can be used to prepare bromobenzene from benzene

(A) NBS (B) Br₂/FeBr₃ (C) H₂SO₄/Br₂ (D) Br₂/AlBr₃ (E) Br₂/Pd

4. Which of the following functional groups are o,p-directing ?

(A) Br, CH₂CH₃, NH₂ (B) Cl, NH₂, COOH (C) I, SO₃H, OH (D) OCH₃, Cl, COCH₃ (E) NO₂, CH₃, OH

5. Which of the following reagent(s) gives the reaction below

(A) CH₃Cl (B) Cl₂/ Fe (C) Cl₂/ AlCl₃ (D) Cl₂/ FeCl₃ (E) Cl₂/ HCl

6. Friedal-Craft acylation reagent(s)

(A) CH₃Cl/AlCl₃ (B) Cl₂/CH₃COCl (C) CH₃COCl/AlCl₃ (D) CH₃COCl/FeCl₃ (E) CH₃Cl/FeCl₃

7. Which of the following functional groups are m-directing ?

(A) NO₂, CH₃, OH (B) Br, NH₂, COOH (C) I, SO₃H, OH (D) OCH₃, Cl, COCH₃ (E) COCH_3, SO₃H, CHO

8. Which of the following compound can be used in the Diels-Alder reaction

(A) 2-methyl, 2,4-hexadiene (B) 2,5-hexadiene (C) 1-methyl,cyclohexa-1,4-diene (D) cyclohexa-1,4-diene

(E) 2-methyl, 1,5-hexadiene

9. Which statement about benzene is incorrect?

(A) The Cï¿½C p - bonding is delocalized (B) The C₆ ring is planar (C) The average C - C bond distance is the same as C-C double bonds (D) Each C atom is sp² hybridized ( E ) There are 12 s (sigma) bonds in benzene

10. Which of the following is NOT aromatic

(A) Cyclopropenyl cation (C₃H₃⁺) (B) Benzene (C₆H₆) (C) [16]-Annulene (C₁₆H₁₆)

(D) Cycloheptatrienyl cation (C₇H₇⁺) (E) [18]-Annulene (C₁₈H₁₈)

11. Conjugate addition of one equivalent of deuterium bromide (DBr) to 1,3-butadiene gives

(A) 3-bromo, 4-deutero, 1-butene (B) 3-bromo, 4-deutero, 2-butene (C) 4-bromo, 3-deutero, 1-butene (D) 1-bromo, 4-deutero, 2-butene (E) 1-bromo, 4-deutero, 1-butene

12. Which of the following is a conjugated diene

(A) cyclopentadiene (B) 2-methylcyclohexanone (C) 1-methyl,cyclohexa-1,4-diene (D) cyclohexa-1,4-diene

(E) cycloocta-1,5-diene

13. The aromatic compound is

14. Which of the following reaction involves a benzyne mechanism ?

(A) Ph-CH₃ ? Ph-COOH (B) Ph-CH₃ ? Ph-CHO (C) Ph-OH ? Ph-Cl (D) Ph-Cl ? Ph-OH

(E) none of these

15. Which of the following reagent(s) can be used to prepare a mixture of o and p-nitro toluene from

toluene

(A) HNO₂ (B) HNO₃ (C) HNO₃/Fe (D) HNO₃/H₂SO₄ (E) NaNO₂

16. Friedal-Craft alkyation reagent(s)

(A) C₂H₅Cl/AlCl₃ (B) Cl₂/CH₃COCl (C) CH₃COCl/AlCl₃ (D) CH₃COCl/FeCl₃ (E) CH₃Cl/FeCl₃

17. Which of the following functional groups are o,p-directing ?

(A) NO₂, SO₃H, CHO (B) Br, NH₂, COOH (C) I, OH, CH₃ (D) OCH₃, Cl, COCH₃ (E) COCH_3, SO₃H, Br

18. Major product in the reaction of benzene with 1-bromopropane, in the presence of AlBr₃ catalyst

(A) bromobenzene (B) n-propylbenzene (C) iso-propylbenzene (D) o-bromo-n-propylbenzene

(E) p-bromo-n-propylbenzene

19. Which of the following is the electrophile in the nitration reaction

(A) ⁺HNO₂ (B) NO₂⁺ (C) N₂+ (D) HNO₃/H₂SO₄ (E) NO₃⁺

20. Which of the following is the electrophile in the sulfonation reaction

(A) ⁺HSO₂ (B) SO₂⁺ (C) SO₃⁺ (D) SO₃/H₂SO₄ (E) HSO₃⁺

21. Which of the following is the electrophile in the Friedel-Craft acylation reaction

(A) RCO₂⁺ (B) RCO⁺ (C) CO₂⁺ (D) RX/H₂SO₄ (E) RCO₃⁺

22. The benzyne intermediate has ï¿½ï¿½ p bonds

(A) 1 (B) 2 (C) 3 (D) 4 (E) 5

23. The reagent used for Allylic/benzylic bromination is:

(A) NBS (B) Br₂/ Fe (C) Br₂/ AlBr₃ (D) Br₂/ FeBr₃ (E) Br₂/ HBr

24. Which of the following is an oxidation reagent

(A) H₂SO₄ (B) KMnO₄ (C) KMnO₂ (D) NaBH₄ (E) AlCl₃

25. The formula of fuming sulfuric acid

(A) H₂SO_4.SO₃ (B) H₂SO_4.SO₂ (C) H₂SO_4.HSO₂ (D) H₂SO_4.HSO₃ (E) H₂SO_4.SO

26. How do you prepare the following compounds, starting from benzene ?

(a). aniline (b). Iodo benzene (c). benzoic acid (d). benzylbromide (e). m-methyl benzoic acid

(f). p-nitrobenzoic acid (g) m-nitrobenzoic acid (h). p-chlorobenzenesulfonic acid (i). m-chlorobenzenesulfonic

acid (j) 3-isopropyl benzoic acid (k). 4-isopropyl toluene

27. Draw the product(s) from the following reactions showing the mechanisms

(a) 1,3-butadiene with acrylonitrile

(b) 1,3-butadiene with one eqv. HBr

(d) 1,3-cyclohexadiene with one eqv. HBr

(e) 1,3-cyclohexadiene with two eqv. HBr

(f) cyclopentadiene with two eqv. HBr

28. How do you prepare the following compounds, starting from toluene ?

(a). benzoic acid (b). benzyl alcohol (c). m-bromobenzoic acid (d). m-methylbenzoic acid (e). m-nitro

benzoic acid (f). p-nitrobenzoic acid

29. What is/are the product(s) expected when ethylbenzene is reacted with

(a). NBS

(b). Br₂/FeBr₃

(c). KMnO₄, then H⁺

(d). fuming H₂SO₄

(e). NBS, then aq. NaOH

(f) iso-butylbromide/AlBr₃

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