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Answer the following questions as thoroughly as you can in preparation for the Friday Quiz. 1....
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1)...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
833 17-10 The Friedel-Crafts Alkylation 1.2NaOH 100 °C 2. H,09 o Zn(Hg) dilute HCI NBS hy...
833 17-10 The Friedel-Crafts Alkylation 1.2NaOH 100 °C 2. H,09 o Zn(Hg) dilute HCI NBS hy NO, Zn HCI C 17-10 The Friedel-Crafts Alkylation U 8. Predict the major product or products for the following reactions. Assume reagents are present in excess amounts unless otherwise indicated. Clearly depict any stereochemistry. "No Reaction is a possible answer. (4 points) each et :O 1 SO, H2SO4 CH2 CH3 сH,CH,CI AICI, NO2 Br FeBrz OH AICI 1 cq Bry FeBr
1. Provide the major organic product(s) for each of the following reactions: 1) HNOZ/H, SO 2)...
1. Provide the major organic product(s) for each of the following reactions: 1) HNOZ/H, SO 2) Sn/HCl(aq) 3) HO 1) (CH3)2CHCI/AICI: 2) NBS/hv 1) Cly/FeCl3 2) HNO,/H2SO4 1) CH3CH,COCI/AICI 2) H20 оооооооо 3) Zn(Hg)/HCl(aq) 1) SOZ/H,SO 2) Bry/FeBrz 1) (CH3)3CCI/AICI: 2) KMnO/HOIA 2) H30* 1) CH,COCIAICI: 2) H, 3) Bry/FeBry COH 1) SOCI_/pyridine 2) PhCH/AICI 3) H20 1. Br JFeBry 2. Mg/Eto 3. oxirane 4, HO* 1) Bry/FeBry 2) s09/H230 1) NBS/hv 2) PhoNa (1 CH3COCI / AIC وا (2...
PLEASE ANSWER ALL QUESTIONS 41) Provide the major organic product of the following reaction. Bry, FeBry...
PLEASE ANSWER ALL QUESTIONS
41) Provide the major organic product of the following reaction. Bry, FeBry 42) Provide the major organic product that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3. Answer: NO2 43) Explain why Friedel-Crafts alkylation reactions are prone to poly alkylation, whereas Friedel- Crafts acylation reactions are not prone to polyacylation? 44) Which series of reagents would be required to perform the following synthesis? A) 1. CICH2CH2CH3, AICI;...
answer any that you can please B. Effect of substituents on EAS B1. Rank each of...
answer any that you can please
B. Effect of substituents on EAS B1. Rank each of the following sets from the most reactive (+1) to the least reactive (4) act more DANHAS CH WA B2. Predict the major product for the following reactions. If there is no reaction, write 'R' NO, C AICI: nog do m HOS нoss B Bra FeBig CHCI La AICI Falkijan we do 0, WALD 0.0 NO, HNO3 ON ON Brz FeBig OH H,SO C. Synthesis...
PLEASE ANSWER ALL QUESTIONS 34) Which sequence correctly ranks the following aromatic rings in order of...
PLEASE ANSWER ALL QUESTIONS
34) Which sequence correctly ranks the following aromatic rings in order of increasing rate of reactivity in an electrophilic aromatic substitution reaction? LOCH A) 1<2<3 B) 2 <3 <1 C) 3 <1<2 D) 2 <1<3 35) Derivatives of the compound shown below are currently being examined for their effectiveness in treating drug addiction and metabolic syndrome (J. Med. Chem. 2006, 872). Which sequence ranks the following aromatic rings of this compound in order of increasing reactivity...
Can you explain how you came upon the answer also 1. Rank the following compounds in...
Can you explain how you came upon the answer also
1. Rank the following compounds in order of increasing stability (least to most stable). As you answer this question, think of why (give reasons) one molecule is more or less stable than another. 2. Predict the MAJOR product(s) for the reaction below. Pay close attention to stereochemistry. Provide a mechanism as to how you arrive with your answer. If your compound is chiral, indicate the configuration [(R) or (S)] of...
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
833 17-10 The Friedel-Crafts Alkylation 1.2NaOH 100 °C 2. H,09 o Zn(Hg) dilute HCI NBS hy NO, Zn HCI C 17-10 The Friedel-Crafts Alkylation U 8. Predict the major product or products for the following reactions. Assume reagents are present in excess amounts unless otherwise indicated. Clearly depict any stereochemistry. "No Reaction is a possible answer. (4 points) each et :O 1 SO, H2SO4 CH2 CH3 сH,CH,CI AICI, NO2 Br FeBrz OH AICI 1 cq Bry FeBr
1. Provide the major organic product(s) for each of the following reactions: 1) HNOZ/H, SO 2) Sn/HCl(aq) 3) HO 1) (CH3)2CHCI/AICI: 2) NBS/hv 1) Cly/FeCl3 2) HNO,/H2SO4 1) CH3CH,COCI/AICI 2) H20 оооооооо 3) Zn(Hg)/HCl(aq) 1) SOZ/H,SO 2) Bry/FeBrz 1) (CH3)3CCI/AICI: 2) KMnO/HOIA 2) H30* 1) CH,COCIAICI: 2) H, 3) Bry/FeBry COH 1) SOCI_/pyridine 2) PhCH/AICI 3) H20 1. Br JFeBry 2. Mg/Eto 3. oxirane 4, HO* 1) Bry/FeBry 2) s09/H230 1) NBS/hv 2) PhoNa (1 CH3COCI / AIC وا (2...
PLEASE ANSWER ALL QUESTIONS
41) Provide the major organic product of the following reaction. Bry, FeBry 42) Provide the major organic product that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3. Answer: NO2 43) Explain why Friedel-Crafts alkylation reactions are prone to poly alkylation, whereas Friedel- Crafts acylation reactions are not prone to polyacylation? 44) Which series of reagents would be required to perform the following synthesis? A) 1. CICH2CH2CH3, AICI;...
answer any that you can please
B. Effect of substituents on EAS B1. Rank each of the following sets from the most reactive (+1) to the least reactive (4) act more DANHAS CH WA B2. Predict the major product for the following reactions. If there is no reaction, write 'R' NO, C AICI: nog do m HOS нoss B Bra FeBig CHCI La AICI Falkijan we do 0, WALD 0.0 NO, HNO3 ON ON Brz FeBig OH H,SO C. Synthesis...
PLEASE ANSWER ALL QUESTIONS
34) Which sequence correctly ranks the following aromatic rings in order of increasing rate of reactivity in an electrophilic aromatic substitution reaction? LOCH A) 1<2<3 B) 2 <3 <1 C) 3 <1<2 D) 2 <1<3 35) Derivatives of the compound shown below are currently being examined for their effectiveness in treating drug addiction and metabolic syndrome (J. Med. Chem. 2006, 872). Which sequence ranks the following aromatic rings of this compound in order of increasing reactivity...
Can you explain how you came upon the answer also
1. Rank the following compounds in order of increasing stability (least to most stable). As you answer this question, think of why (give reasons) one molecule is more or less stable than another. 2. Predict the MAJOR product(s) for the reaction below. Pay close attention to stereochemistry. Provide a mechanism as to how you arrive with your answer. If your compound is chiral, indicate the configuration [(R) or (S)] of...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
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