Tetracaine can be synthesized from benzene. The synthesis involves the following steps:
Benzene + CH3Cl, AlCl3 to form product A;
A + HNO3, H2SO4 to form product B;
B + KMnO4, H2O to form product C;
C + SOCl2 to form product D;
D + HOCH2CH2N(CH3)2 to form product E;
E + H2, Pt to form product F;
F + CH3CH2CH2CHO to form product G;
G + NaBH3CN to form Tetracaine.
Draw the structures of product A and product G.
Tetracaine can be synthesized from benzene. The synthesis involves the following steps: Benzene + CH3Cl, AlCl3...
Tetracaine can be synthesized from benzene. The synthesis involves the following steps: Benzene + CH3Cl, AlCl3 to form product A; A + HNO3, H2SO4 to form product B; B + KMnO4, H2O to form product C; C + SOCl2 to form product D; D + HOCH2CH2N(CH3)2 to form product E; E + H2, Pt to form product F; F + CH3CH2CH2CHO to form product G; G + NaBH3CN to form Tetracaine. Draw the structures of product C and product F.
3) Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction with 1,3-butadiene? A) CH2CHOCH3 B) CH2CHCHO C) CH3CHCHCH3 D) (CH3)2CCH2 E) CH2CH2 5) Which of the following fails to form benzoic acid when heated with chromic acid? A) 1-phenylethanol B) 2-phenylethanol C) 2-phenylheptane D) 2-methyl-2-phenylheptane E) 1-phenylheptanol 11) How can the following synthesis be carried out? A) HCOOH; HNO3/H2SO4 B) CH3Cl/AlCl3; HNO3/H2SO4; H2CrO4, heat C) CH3Cl/AlCl3; H2CrO4, heat; HNO3/H2SO4 D) HNO3/H2SO4; CH3Cl/AlCl3; H2CrO4, heat E)...
Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. Step 1=? Step 2=? Step 3=? Step 4=? Step 5=? Options for each step: Br2, R2O2 CH3Cl, AlCl3 CH3COCl, AlCl3 NaNO2, HCl HNO3, H2SO4 H3PO2 H3PO4 KMnO4 1) Sn, HCl; 2)OH- Br2 Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from...
Starting with benzene what is the major product to the following reagents. 1. Br2/FeBr3, (CH3)2CCOCl/AlCl3 2. (CH3)2CCOCl/AlCl3, Br2/FeBr3 3. Br2/FeBr3, H2SO4, (CH3)2CCOCl/AlCl3, H2O Which major product of the three will give the most one product if reacted with HNO3/H2SO4?
Synthesis of target compound starting from benzene. Assume all reactions are appropriately worked up and that mixtures of constitutional isomers can be separated. May use a reagent more than once if needed. A. Cly/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H2Cr04 J. 1)LiAlH42)H2O K. H/Ni L. 1) Mg 2)CO2 3)H30* M. CH3OH/H30* N. (CH3)2SO4 NaOH 0. CH3OH P. SOCl2 Q. HC1 R. NaN3 -NH₂ CI
What are the steps that give this product given the reagent list. Multistop Synthesis NH₂ A. Cl2/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO2/HCI E. HC1/Cuci F, KCN/CuCN G. H3PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H20 K. H/Ni L. 1) Mg 2)CO2 3)H30 M. CH3OH/H30* N. (CH3)2SO4 NaOH 0. CH3OH P. SOCl2 Q. HC1 R. NaN3
Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. (All drop down menus have the same reagants). Benzene can be converted to 1,3,5-tribromobenzene in five reaction steps and four intermediate compounds. Select the appropriate reagent from the drop-down list for each step in this overall synthesis. Step 1 Step 2 Step 3 Step 4 Step 5 Br Br Br Reagents...
5. You want to synthesize meta-chlorotoluene from benzene. You can use the following reactions: 1. CH3COCl/AlCl3, 2. CH3Cl/AlCl3, 3. Zn(Hg)/HCl, 4. HNO3/2SO4, 5. Cl2/FeCl3. Determine the order in which you would do this synthesis. E.g., 123 means you would do CH3COCl/AlCl3 first, followed by CH3Cl/AlCl3, and then Zn(Hg)/HCl. Write your answer with a two or three or four or five digit number. Do not use commas or spaces between each digit.
10. How can p-aminobenzoic acid (a sunscreen) be synthesized from benzene? (Note that sometimes more than one isomer will be obtained, which is fine as long as the desired isomer is one of the major products.) several steps HOOC NH2 A)) 1.CH3CI, AİCİ3 3.KMnO4 . CH CI, AICl 4.KMnO 4. Sn, HCI 2. IINO, H2SO4 )1. HNO3, H2SO4 2. Sn, HCI C) 1. HNO, HSO42. CHCI, AIC D) 1. CHCl, AlCl KMO 4.KMnO 4. Sn, HCI 3. Sn, HCI 3....
The following are several steps in the synthesis of an anesthetic: ОН CH3 CH3 A B с ht What reagents are needed to effect the transformation in C? Select one: O a. H2O/cat. H+ O O b. CH3COOH/cat. H* C. CH3CH2OH/cat. H+ d. dilute H2SO4 O What reagents are needed to effect the transformation in A? Select one: a. HNOz/cat. H2S04 b. HNO3/cat. H2S04 c. NaNO3 O d. NaNO2 What reagents are needed to effect the transformation in B? Select...