Fill in the unknown structures below.
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Fill in the unknown structures below.
PRODUCTO PRINCIPAL H20+ 1. BHZ/THF 2. NaOH/H,O, HBEN 1. Mg,...
Brz> A e B + C prine) H₂O7 Hoy 1. KMnO OH 2.H30* 1. BHZ/THF 2....
Brz> A e B + C prine) H₂O7 Hoy 1. KMnO OH 2.H30* 1. BHZ/THF 2. NaOH/H2O2 NaBH4 MeOH 1. BHz/THF PCC F. NOOHHO, E edom D 1. MeMgBr 2.420 Hoy I + Jeroen
NaBH4 CC Hg(OAC)2 H20, THE NaOH 1. Hg(O2CCF3)2, 'ProH 2. NaBH4, NaOH 1. BHz •THF 2....
NaBH4 CC Hg(OAC)2 H20, THE NaOH 1. Hg(O2CCF3)2, 'ProH 2. NaBH4, NaOH 1. BHz •THF 2. H2O2, HOⓇ R-OH + Nax — NaCN DMSO TSCI pyridine ОН MSCI pyridine NasMe DMSO cat. HA MeOH + g. Arrange in the Increasing acidity order HẠO ROH RC=CH HA NHA RH. cold KMnO4, HOor 1. Os04 2. NaHSO3 MICH3 1. mCPBA 2. H+, CH3OH, H2O 1. mCPBA 2. NaOCH3, H20 H2O / H+ Hg(OAC)2 H2O, THE NaBH4 NaOH 1. BH3 THF 2. HaO2...
PCC CH-PP D.CH.Mobi 2) H,0 ICHO, CHO, CH₂₂O; CH,402 1) BHz, THF 2) H2O2, NaOH spontaneous...
PCC CH-PP D.CH.Mobi 2) H,0 ICHO, CHO, CH₂₂O; CH,402 1) BHz, THF 2) H2O2, NaOH spontaneous DISCL pyridine C-Multistriatin (un insect pheromone) Coto, 74 C, , H₂O, Hint: enolate chemistry from chapter 22 CH160, 14 14
1) R'-MgBr in THF 2)H,o NaH Ho or OH PAA X2. H20 1) Hg(OAc)2, R'OH 2)...
1) R'-MgBr in THF 2)H,o NaH Ho or OH PAA X2. H20 1) Hg(OAc)2, R'OH 2) NaBH4, NaOH, H20 Os0 NaHSO, H2O I) 2)CH, SCH HyIO HBr ROOR 1)BH3. THF 2)H202, NaOH, H2O Mg, THF PBr3 NaOH )OTHF 2) H30 CrOj. H,SO, 1) NaH 2)RXDMF "О-R DMF PCC DCM ) THF 2) H3O+ SOCI pyridine Li Hexanes
1. Cl, H20 2. NaOH 3. CH3CH2MgBr 4. H30* 1. Mg 2h) 2. H₃C.. 3. H30+...
1. Cl, H20 2. NaOH 3. CH3CH2MgBr 4. H30* 1. Mg 2h) 2. H₃C.. 3. H30+ 1. SOCI OH 2. DIBAL"H 3. H30* OH 1. NaOH 2j) 2. CH3CH2CI 3. O o 2k) [ N-H H20. STAB OH 2)) 1. NaOH 2. CH3CH,CI 3. O o IN-H 2k) H30*. STAB 21) 1. 2 KCN, HCN 2. LiAlH4 3. H30+ 4. H2, Pt
1) + NaOH J) OH PCC CH,C1, K) H СН,ОН L) 1. Mg, ether -Br o...
1) + NaOH J) OH PCC CH,C1, K) H СН,ОН L) 1. Mg, ether -Br o 2. 3. H,0 M) OH Na Cr 0 H2SO4 4. Propose Mechanism (Show your work) (14 pts) A) CH,CH,CH,OH CHỊCH CHỊCHCHỊCOH
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE...
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE 2.CO 3.NH.CH HNO k.) NH 1. HNO (aq) 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCU. n) -OH XS H.CO acetone он 0.) OH XS Bobbit's SiO, CH.CH -OH 1. Ch. AICI 2 NaOH, 30 C 4,000 psi 3. HCI 9.) SCH 2Na, ETOH, NH, r.) 1. LIETO 2. oxirane 3. H,00 1.2 PY-MOBI OMe 2. NHCl(aq) t.) 1. Cl/ Feer...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number...
Propose an efficient synthesis for the transformation below,
using two sequential reductive aminations. Enter
the appropriate number or letter from the reagent list handout.
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH d.) o 1. XS LAIH/THF/-78 °C 2. H20 H OH e.) NaNH / lig NH3 f.) Br 1. Mg/THE 2. CO2 3. H30 9.) Ph Ph cyclopropene HF CH h.) OH 1. PCCICH.CH 2. Pri 3. N,Cag) 1. LITHF 2.CO 3. NH.Ca) HNO, NH 1. HNO () 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCH n.) OH XS H.COM acetone OH...
Brz> A e B + C prine) H₂O7 Hoy 1. KMnO OH 2.H30* 1. BHZ/THF 2. NaOH/H2O2 NaBH4 MeOH 1. BHz/THF PCC F. NOOHHO, E edom D 1. MeMgBr 2.420 Hoy I + Jeroen
NaBH4 CC Hg(OAC)2 H20, THE NaOH 1. Hg(O2CCF3)2, 'ProH 2. NaBH4, NaOH 1. BHz •THF 2. H2O2, HOⓇ R-OH + Nax — NaCN DMSO TSCI pyridine ОН MSCI pyridine NasMe DMSO cat. HA MeOH + g. Arrange in the Increasing acidity order HẠO ROH RC=CH HA NHA RH. cold KMnO4, HOor 1. Os04 2. NaHSO3 MICH3 1. mCPBA 2. H+, CH3OH, H2O 1. mCPBA 2. NaOCH3, H20 H2O / H+ Hg(OAC)2 H2O, THE NaBH4 NaOH 1. BH3 THF 2. HaO2...
PCC CH-PP D.CH.Mobi 2) H,0 ICHO, CHO, CH₂₂O; CH,402 1) BHz, THF 2) H2O2, NaOH spontaneous DISCL pyridine C-Multistriatin (un insect pheromone) Coto, 74 C, , H₂O, Hint: enolate chemistry from chapter 22 CH160, 14 14
1) R'-MgBr in THF 2)H,o NaH Ho or OH PAA X2. H20 1) Hg(OAc)2, R'OH 2) NaBH4, NaOH, H20 Os0 NaHSO, H2O I) 2)CH, SCH HyIO HBr ROOR 1)BH3. THF 2)H202, NaOH, H2O Mg, THF PBr3 NaOH )OTHF 2) H30 CrOj. H,SO, 1) NaH 2)RXDMF "О-R DMF PCC DCM ) THF 2) H3O+ SOCI pyridine Li Hexanes
1. Cl, H20 2. NaOH 3. CH3CH2MgBr 4. H30* 1. Mg 2h) 2. H₃C.. 3. H30+ 1. SOCI OH 2. DIBAL"H 3. H30* OH 1. NaOH 2j) 2. CH3CH2CI 3. O o 2k) [ N-H H20. STAB OH 2)) 1. NaOH 2. CH3CH,CI 3. O o IN-H 2k) H30*. STAB 21) 1. 2 KCN, HCN 2. LiAlH4 3. H30+ 4. H2, Pt
1) + NaOH J) OH PCC CH,C1, K) H СН,ОН L) 1. Mg, ether -Br o 2. 3. H,0 M) OH Na Cr 0 H2SO4 4. Propose Mechanism (Show your work) (14 pts) A) CH,CH,CH,OH CHỊCH CHỊCHCHỊCOH
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE 2.CO 3.NH.CH HNO k.) NH 1. HNO (aq) 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCU. n) -OH XS H.CO acetone он 0.) OH XS Bobbit's SiO, CH.CH -OH 1. Ch. AICI 2 NaOH, 30 C 4,000 psi 3. HCI 9.) SCH 2Na, ETOH, NH, r.) 1. LIETO 2. oxirane 3. H,00 1.2 PY-MOBI OMe 2. NHCl(aq) t.) 1. Cl/ Feer...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...
Propose an efficient synthesis for the transformation below,
using two sequential reductive aminations. Enter
the appropriate number or letter from the reagent list handout.
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH d.) o 1. XS LAIH/THF/-78 °C 2. H20 H OH e.) NaNH / lig NH3 f.) Br 1. Mg/THE 2. CO2 3. H30 9.) Ph Ph cyclopropene HF CH h.) OH 1. PCCICH.CH 2. Pri 3. N,Cag) 1. LITHF 2.CO 3. NH.Ca) HNO, NH 1. HNO () 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCH n.) OH XS H.COM acetone OH...
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