Homework Answers
1) c) SN1 Nucleophilic substitution
Explanation; opening of epoxide in presence of HBr gives SN1 substitution reaction
2) d) SN2 Nucleophilic substitution
Explanation: The electron density on nitrogen atom of amine gives SN2 substitution reaction.
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он Biosynthesis of adreneline (epinephrine) он a Electrophilic addition b E2 Elimination CSN1 Nucleophilic substitution d-SN2...
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl...
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl Xfer) e-Electrophilic aromatic substitution h -Conjugate (nucleophilic) addn SNI Nucleophilic substitution r-Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Submit Answor Retry Entire Group 9 more group attempts remaining
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a - Proton transfer dSN2 Nucleophilic substitution b- Lewis acid/base e-Electrophilic aromatic substitution c=E2 elimination f= g Nucleophilic subs at...
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a - Proton transfer dSN2 Nucleophilic substitution b- Lewis acid/base e-Electrophilic aromatic substitution c=E2 elimination f= g Nucleophilic subs at carbonyl(acyl Xfer) h-Conjugate (nucleophilic) addn r-carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a i for your answers. 1. 2.
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a -...
CO2H CO2H HNO3/H2SO4 H20 2. +conc. HBr H20 Br OH a Electrophilic addition b E2 Elimination...
CO2H CO2H HNO3/H2SO4 H20 2. +conc. HBr H20 Br OH a Electrophilic addition b E2 Elimination c-SNI Nucleophilic substitution d S2 Nucleophilic substitution e-Electrophilic aromatic substitution f-carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn for your answers 1. 2.
aqueous NaOH HCCl CCl3 O Na 2. OH HCI но d-SN2 Nucleophilic subst e - Carbonyl...
aqueous NaOH HCCl CCl3 O Na 2. OH HCI но d-SN2 Nucleophilic subst e - Carbonyl nucleophilic addn f= Nucleophilic subs at carbonyl(acyl Xfer) g-Conjugate (nucleophilic) addn a-Electrophilic addition - E2 Elimination C-SNI Nucleophilic subst Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers 1. 2. он Na HSO3 SO3 Na O2C citrate synthase COA CH2 CO2 CH2 O CO2 Acetyl coenzyme A Oxaloacetate...
Help! 1. 1. LIAIH4 / dry ether он 2. aqueous H2S04 2. AICl3 Ci но dSN2...
Help!
1. 1. LIAIH4 / dry ether он 2. aqueous H2S04 2. AICl3 Ci но dSN2 Nucleophilic substitutiong a = Electrophilic addition b E2 Elimination c SN1 Nucleophilic substitution f Carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Review Topics] 1. HCI reflux он +...
HEN + H₂O 1 гсны CH HO NaOH Ph afra 2. a = Electrophilic addition d...
HEN + H₂O 1 гсны CH HO NaOH Ph afra 2. a = Electrophilic addition d = Sy2 Nucleophilic substitution b = E2 Elimination e-Electrophilic aromatic substitution c=S91 Nucleophilic substitution 1= Carbonyl nucleophilic addn g=Nucleophilic subs at carbonyl(acyl Xfer) h - Conjugate (nucleophilie) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters at for your answers 1
Na 1. Br CH2-Ph 2. Ph 6M HC OH он NH CI NHy CI NH d...
Na 1. Br CH2-Ph 2. Ph 6M HC OH он NH CI NHy CI NH d -Sy2 Nucleophilic substitution Nucleophilic subs at carbonyl(acyl Xfer) a Electrophilic addition b- E2 Elimination e-Syl Nucleophilic substitution e Electrophilic aromatic substitution h Conjugate (nucleophilic) addn r-Carbonyl nucleophilie addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 2. Submit Answer Ratry Entiro Group 0 1. Cl 0 OMe...
a = Proton transfer b = Lewis acid/base c = E2 elimination d = S_N 2...
a = Proton transfer b = Lewis acid/base c = E2 elimination d = S_N 2 Nucleophile substitution e = Electrophilic aromatic substitution f = Carbonyl nucleophilie addin g = nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identity the mechanism by which each of the reactions above proceeds from among the mechanisms listed Use the letters a - i for your answers
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2...
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2 elimination d SN2 Nucleophilic substitution e-Electrophilic aromatic substitution f Carbonyl nucleophilic addn g Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. 1.8% Hyc's、CH, + H CH3 2. N(CHs CI a Proton transfer b-Lewis acid/base E2...
1. Br Acetone Nal NaBr NaOEt CN 2. es CN a = Electrophilic addition b=E2 Elimination...
1. Br Acetone Nal NaBr NaOEt CN 2. es CN a = Electrophilic addition b=E2 Elimination c=Snl Nucleophilic subst d = Sy2 Nucleophilic subst e=Carbonyl nucleophilic addn f= Nucleophilic subs at carbonyl(acyl Xfer) g = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2.
O H2N-OH 2. нса a Electrophilic addition b-E2 Elimination d- Sy2 Nucleophilic substitution-Nucleophilic subs at carbonyl(acyl Xfer) e-Electrophilic aromatic substitution h -Conjugate (nucleophilic) addn SNI Nucleophilic substitution r-Carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Submit Answor Retry Entire Group 9 more group attempts remaining
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a - Proton transfer dSN2 Nucleophilic substitution b- Lewis acid/base e-Electrophilic aromatic substitution c=E2 elimination f= g Nucleophilic subs at carbonyl(acyl Xfer) h-Conjugate (nucleophilic) addn r-carbonyl nucleophilic addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a i for your answers. 1. 2.
N(CH3)3 OH 1. heat 95% 5% (E & Z) он 2. H2N a -...
CO2H CO2H HNO3/H2SO4 H20 2. +conc. HBr H20 Br OH a Electrophilic addition b E2 Elimination c-SNI Nucleophilic substitution d S2 Nucleophilic substitution e-Electrophilic aromatic substitution f-carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn for your answers 1. 2.
aqueous NaOH HCCl CCl3 O Na 2. OH HCI но d-SN2 Nucleophilic subst e - Carbonyl nucleophilic addn f= Nucleophilic subs at carbonyl(acyl Xfer) g-Conjugate (nucleophilic) addn a-Electrophilic addition - E2 Elimination C-SNI Nucleophilic subst Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers 1. 2. он Na HSO3 SO3 Na O2C citrate synthase COA CH2 CO2 CH2 O CO2 Acetyl coenzyme A Oxaloacetate...
Help!
1. 1. LIAIH4 / dry ether он 2. aqueous H2S04 2. AICl3 Ci но dSN2 Nucleophilic substitutiong a = Electrophilic addition b E2 Elimination c SN1 Nucleophilic substitution f Carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Review Topics] 1. HCI reflux он +...
HEN + H₂O 1 гсны CH HO NaOH Ph afra 2. a = Electrophilic addition d = Sy2 Nucleophilic substitution b = E2 Elimination e-Electrophilic aromatic substitution c=S91 Nucleophilic substitution 1= Carbonyl nucleophilic addn g=Nucleophilic subs at carbonyl(acyl Xfer) h - Conjugate (nucleophilie) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters at for your answers 1
Na 1. Br CH2-Ph 2. Ph 6M HC OH он NH CI NHy CI NH d -Sy2 Nucleophilic substitution Nucleophilic subs at carbonyl(acyl Xfer) a Electrophilic addition b- E2 Elimination e-Syl Nucleophilic substitution e Electrophilic aromatic substitution h Conjugate (nucleophilic) addn r-Carbonyl nucleophilie addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 2. Submit Answer Ratry Entiro Group 0 1. Cl 0 OMe...
a = Proton transfer b = Lewis acid/base c = E2 elimination d = S_N 2 Nucleophile substitution e = Electrophilic aromatic substitution f = Carbonyl nucleophilie addin g = nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identity the mechanism by which each of the reactions above proceeds from among the mechanisms listed Use the letters a - i for your answers
1. Li 2. aq. NaOH reflux Cl NaCI+H20 a Proton transfer b Lewis acid/base c E2 elimination d SN2 Nucleophilic substitution e-Electrophilic aromatic substitution f Carbonyl nucleophilic addn g Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. 1.8% Hyc's、CH, + H CH3 2. N(CHs CI a Proton transfer b-Lewis acid/base E2...
1. Br Acetone Nal NaBr NaOEt CN 2. es CN a = Electrophilic addition b=E2 Elimination c=Snl Nucleophilic subst d = Sy2 Nucleophilic subst e=Carbonyl nucleophilic addn f= Nucleophilic subs at carbonyl(acyl Xfer) g = Conjugate (nucleophilic) addn Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2.
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