Homework Answers
Multiple sub-parts, as per guideline only first 4 will be answered (4a-4d) :
a.' P' attacks with its lone pair, with expulsion of of chloride ion.Cl- captures methyl group from methoxy , leading to product.
b. Both enantiomers gives different products, via non-classical cabocation.
c. Proton from acid attacks to triple bond,Cl assists in reaction : leading to product.
d. Compounds gives different product based on position of leaving group.
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4.2. Suggest reasonable mechanisms for each of the following reactions. The starting materials are racemic, unless...
4.1.3 X 10', n = 5:4.3. 4.2. Suggest reasonable mechanisms for each of the following reactions....
4.1.3 X 10', n = 5:4.3. 4.2. Suggest reasonable mechanisms for each of the following reactions. The materials are racemic, unless otherwise stated. ctions. The starting PHCHCI + PLOCH)3 = PhCH P(OC Hs)2 + CHCI CH CH. CH O H BSCI CH, CH₂ CH₂ CH CH but Bsci "OH pyridine CH Bso pyridine Bso HCBCCH CHỊCHCI - HẠC CCHỊCH,CHẠOCF O NaNO,H,O HCIO CH=o bự (CH4)ẠCAM-OH NaNO2, H2O NH, HCIO (CH) CH CHE (Ac), CHON H, heat but but OH (Ac),...
Suggest a reasonable mechanism for each of the following reactions. The starting materials are racemic, unless...
Suggest a reasonable mechanism for each of the following
reactions. The starting materials are racemic, unless otherwise
stated
(PhC)2NCH2CH2C CH2CN, H2O heat PhCNHCH2CH2O2CPh
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
II. Draw the structure for the major organic product of each of the following reactions. (7.5...
II. Draw the structure for the major organic product of each of the following reactions. (7.5 pts each, 45 pts) Ç(CH3) 30 1) PhČCI, AICI: 11. 2) Et2NH, H2, Raney-Ni, heat 12. ÇO,Me 1) EtMgBr (2 equiv.) 2) H20, H30* O 13. CNH2 1) Bry, NaOH, H,0 O 2) (CH3)2CHCCI, pyridine 14. Brą, H20 CHO HOEH H HOH НЕОН HO+H CH OH 15. H2N. ***** оо CO2 1) (CH3),COCOCOC(CH3)3 2) -N: C: NH- 16. CHO нон PhNHNH2 H+OH (3 equiv.)...
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...
thanks! On each the following IR spectra, circle and indicate the most important stretching signal from...
thanks!
On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 C-OR Characteristic IR Stretching Frequencies in cm broad N-H 0-H CEN (3000-3500) (2200-2400) 4000 3000 2000 (1150-1300) 요 RC-O (1600-1750) (1250-1350) (1050-1150) 1500 1000 500 'H-NMR...
II. Draw the structure for the major organic product of each of the following reactions. (7.5...
II. Draw the structure for the major organic product of each of the following reactions. (7.5 pts each, 45 pts) Ç(CH3)3 0 11. 1) PhCCI, AICI: 2) Et2NH, H2, Raney-Ni, heat 12. co Me 1) EtMgBr (2 equiv.) 2) H2O, H30* 13. o CNH, 1) Bra, NaOH, HẠO o 2) (CH3)CHČCI, pyridine 14. CHO Но+н HTOH Br2, H20 н+ОН НО-НН CH OH 4
II. Draw the structure for the major organic product of each of the following reactions. (7.5...
II. Draw the structure for the major organic product of each of the following reactions. (7.5 pts each, 45 pts) Ç(CH3)3 0 11. 1) PhCCI, AICI: 2) Et2NH, H2, Raney-Ni, heat 12. co Me 1) EtMgBr (2 equiv.) 2) H2O, H30* 13. o CNH, 1) Bra, NaOH, HẠO o 2) (CH3)CHČCI, pyridine 14. CHO Но+н HTOH Br2, H20 н+ОН НО-НН CH OH 4
Thanks! On each the following IR spectra, circle and indicate the most important stretching signal from...
Thanks!
On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) 30 Unsat. Index = (2C+2-H-X+NY2 = 200 25 e = 2.00 ppm, 4.90 f = 1.27 ppm, 20 720 Compound 18a: C,H,O, singlet, 2H triplet, 3H 127 15 d = 2.66 ppm, a = 7.21 ppm, b = 7.18 ppm, doublet, 2H doublet, 2H C = 4.90...
4.1.3 X 10', n = 5:4.3. 4.2. Suggest reasonable mechanisms for each of the following reactions. The materials are racemic, unless otherwise stated. ctions. The starting PHCHCI + PLOCH)3 = PhCH P(OC Hs)2 + CHCI CH CH. CH O H BSCI CH, CH₂ CH₂ CH CH but Bsci "OH pyridine CH Bso pyridine Bso HCBCCH CHỊCHCI - HẠC CCHỊCH,CHẠOCF O NaNO,H,O HCIO CH=o bự (CH4)ẠCAM-OH NaNO2, H2O NH, HCIO (CH) CH CHE (Ac), CHON H, heat but but OH (Ac),...
Suggest a reasonable mechanism for each of the following
reactions. The starting materials are racemic, unless otherwise
stated
(PhC)2NCH2CH2C CH2CN, H2O heat PhCNHCH2CH2O2CPh
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
II. Draw the structure for the major organic product of each of the following reactions. (7.5 pts each, 45 pts) Ç(CH3) 30 1) PhČCI, AICI: 11. 2) Et2NH, H2, Raney-Ni, heat 12. ÇO,Me 1) EtMgBr (2 equiv.) 2) H20, H30* O 13. CNH2 1) Bry, NaOH, H,0 O 2) (CH3)2CHCCI, pyridine 14. Brą, H20 CHO HOEH H HOH НЕОН HO+H CH OH 15. H2N. ***** оо CO2 1) (CH3),COCOCOC(CH3)3 2) -N: C: NH- 16. CHO нон PhNHNH2 H+OH (3 equiv.)...
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...
thanks!
On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 C-OR Characteristic IR Stretching Frequencies in cm broad N-H 0-H CEN (3000-3500) (2200-2400) 4000 3000 2000 (1150-1300) 요 RC-O (1600-1750) (1250-1350) (1050-1150) 1500 1000 500 'H-NMR...
II. Draw the structure for the major organic product of each of the following reactions. (7.5 pts each, 45 pts) Ç(CH3)3 0 11. 1) PhCCI, AICI: 2) Et2NH, H2, Raney-Ni, heat 12. co Me 1) EtMgBr (2 equiv.) 2) H2O, H30* 13. o CNH, 1) Bra, NaOH, HẠO o 2) (CH3)CHČCI, pyridine 14. CHO Но+н HTOH Br2, H20 н+ОН НО-НН CH OH 4
II. Draw the structure for the major organic product of each of the following reactions. (7.5 pts each, 45 pts) Ç(CH3)3 0 11. 1) PhCCI, AICI: 2) Et2NH, H2, Raney-Ni, heat 12. co Me 1) EtMgBr (2 equiv.) 2) H2O, H30* 13. o CNH, 1) Bra, NaOH, HẠO o 2) (CH3)CHČCI, pyridine 14. CHO Но+н HTOH Br2, H20 н+ОН НО-НН CH OH 4
Thanks!
On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) 30 Unsat. Index = (2C+2-H-X+NY2 = 200 25 e = 2.00 ppm, 4.90 f = 1.27 ppm, 20 720 Compound 18a: C,H,O, singlet, 2H triplet, 3H 127 15 d = 2.66 ppm, a = 7.21 ppm, b = 7.18 ppm, doublet, 2H doublet, 2H C = 4.90...
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