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Need Help. Will Rate If Complete.
NaOH, H20 н NaOH, H20 Н СНО 1) LDA (1.1...
Need Help. Will Rate If Complete. NaOH, H20 wborn Bonaparte 1) NaOPr, ProH 2) H30+ OMe...
Need Help. Will Rate If Complete.
NaOH, H20 wborn Bonaparte 1) NaOPr, ProH 2) H30+ OMe 1) NaoMe, MeOH Ome 2) H30+ 1) LDA (1.1 eq) 2) Et 3) H20 1) NaOEt, EtOH 2) H30 Eto OEt COOEt COOEt 1) NaOet, EtOH 2) H2O
Predict the products for the following reactions. Note – think about the base being used – is it catalytic? If so, can t...
Predict the products for the following reactions. Note – think
about the base being used – is it catalytic? If so, can the product
molecule ring-close?
NaOEt OEt 1) Ph,CuLi, -78°C 2) H20 1) NaOEt EtO OEt 2) NaOH/H20 3) HСИН20 4) Heat 1) R2NH, H 2) H 3) Н,о" 1) R2NH, H* Ph 2) 3) Нзо*
NaOEt OEt 1) Ph,CuLi, -78°C 2) H20 1) NaOEt EtO OEt 2) NaOH/H20 3) HСИН20 4) Heat 1) R2NH, H 2) H 3)...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2)...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
pls do B to P thanks HCFO AIC Br CH O A (Substitution) NO 1) LDA...
pls do B to P thanks
HCFO AIC Br CH O A (Substitution) NO 1) LDA 2) H,о* 1) NaOh 2) 3) H5o', A 2) нCL H,о H then H.O EIMgBr H 1) Eto 2) но", А EtO OEt CN NaH J Br LDA/THF K -78 °C Br LDATHF L 0°C Br S H2 Raney Ni M 1) CF COOOH 2) LIAIH N Ph.PECHCH ETOH P HCI
HCFO AIC Br CH O A (Substitution) NO 1) LDA 2) H,о* 1)...
4. Draw the products of the following sequences of reactions. 1) NaOET, HOE 1) NaOEt Eto...
4. Draw the products of the following sequences of reactions. 1) NaOET, HOE 1) NaOEt Eto OEt 2) H3O+ 2) Br | 1) LDA, -78°C 2) 0 H30+ heat H 3) NaOH, heat 1) LDA (1.1 equiv), -78°C, THE 2) CH3Br 1) CH3CH2MgBr 2) H30* H2, Pd-C LU H2SO4 NaOH, H2O 1) LDA, -78°C 2) HOE 3) H30+ 1) O3 2) CH2SCH3
OH r. Он reagent(s) Br OEt S. reagent(s) Br Он K2Cr2O7 (excess) H2SO4, H20 Он но...
OH r. Он reagent(s) Br OEt S. reagent(s) Br Он K2Cr2O7 (excess) H2SO4, H20 Он но 1. PhLi, Et O 2. HCI, H2O 3. SOCI2, EtN 4. NaOAc u. н 1. Mg (1 eq), Et2O V. Br 2. (1 eq) -сно 3. HCI, Н,О W. 1. NaBH,, MeOН, 0° С 2. PBra THF 3. LIAID4, THF 4. HCI, H20
Predict the products for each reaction shown below N NaOH N NaOH THF LDA 1) NaH,...
Predict the products for each reaction shown below N NaOH N NaOH THF LDA 1) NaH, THF EtO THF-78 °C 2) CH3CH2Br heat HO CH3COOH KOH CH3NH2 KOH MeOH 1) NaOMe, MeOH 1) HCI, H20 OH 2) PhCH2Br 2) 180 °C
le chatelier experimen Thursday). 1. What starting material and reagents are needed for the following multi-s...
le
chatelier experimen
Thursday). 1. What starting material and reagents are needed for the following multi-step synthesis (HINT: aldol reactions work best when the starting material can only form one enolate)? 5 он о D. NaOH, H2O, Heat F. HO E. NaOH, H2O G. LDA Starting Material: Reagents: 2. LDA is a strong, sterically hindered base and will form the enolate. Sodium hydride is a weak base and will form the _ - enolate. Kinetic enolates are the stable and...
(more synthesis, continued. 2 points each) 2 Bra 2 NaOH Ph water g. 1. LDA 1....
(more synthesis, continued. 2 points each) 2 Bra 2 NaOH Ph water g. 1. LDA 1. NaOCHs CHOH 2. BrCH CH2CHs 3. H', H20, heat H Ph (warmup, long time) NaOEt k. OEt EtOH 1. PPhs Br 2. BuLi 3.
28 - Fill in the hal ini tersing a 08 - Fill in the boxes with...
28 - Fill in the hal ini tersing a 08 - Fill in the boxes with the product(s) for the following reactions. Draw only the predominate regioisomer and indicate the stereochemistry where appropriate. If a racemic mixture is formed, you may indicate this using a wavy line or mark the chiral center with an asterisk (*), and write racemic in the box. 1) NaOPr, ProH 2) H307 1) NaoMe, MeOH OMe 2) H30+ 1) LDA (1.1 eq) 2) OEt 3)...
Need Help. Will Rate If Complete.
NaOH, H20 wborn Bonaparte 1) NaOPr, ProH 2) H30+ OMe 1) NaoMe, MeOH Ome 2) H30+ 1) LDA (1.1 eq) 2) Et 3) H20 1) NaOEt, EtOH 2) H30 Eto OEt COOEt COOEt 1) NaOet, EtOH 2) H2O
Predict the products for the following reactions. Note – think
about the base being used – is it catalytic? If so, can the product
molecule ring-close?
NaOEt OEt 1) Ph,CuLi, -78°C 2) H20 1) NaOEt EtO OEt 2) NaOH/H20 3) HСИН20 4) Heat 1) R2NH, H 2) H 3) Н,о" 1) R2NH, H* Ph 2) 3) Нзо*
NaOEt OEt 1) Ph,CuLi, -78°C 2) H20 1) NaOEt EtO OEt 2) NaOH/H20 3) HСИН20 4) Heat 1) R2NH, H 2) H 3)...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
pls do B to P thanks
HCFO AIC Br CH O A (Substitution) NO 1) LDA 2) H,о* 1) NaOh 2) 3) H5o', A 2) нCL H,о H then H.O EIMgBr H 1) Eto 2) но", А EtO OEt CN NaH J Br LDA/THF K -78 °C Br LDATHF L 0°C Br S H2 Raney Ni M 1) CF COOOH 2) LIAIH N Ph.PECHCH ETOH P HCI
HCFO AIC Br CH O A (Substitution) NO 1) LDA 2) H,о* 1)...
4. Draw the products of the following sequences of reactions. 1) NaOET, HOE 1) NaOEt Eto OEt 2) H3O+ 2) Br | 1) LDA, -78°C 2) 0 H30+ heat H 3) NaOH, heat 1) LDA (1.1 equiv), -78°C, THE 2) CH3Br 1) CH3CH2MgBr 2) H30* H2, Pd-C LU H2SO4 NaOH, H2O 1) LDA, -78°C 2) HOE 3) H30+ 1) O3 2) CH2SCH3
OH r. Он reagent(s) Br OEt S. reagent(s) Br Он K2Cr2O7 (excess) H2SO4, H20 Он но 1. PhLi, Et O 2. HCI, H2O 3. SOCI2, EtN 4. NaOAc u. н 1. Mg (1 eq), Et2O V. Br 2. (1 eq) -сно 3. HCI, Н,О W. 1. NaBH,, MeOН, 0° С 2. PBra THF 3. LIAID4, THF 4. HCI, H20
Predict the products for each reaction shown below N NaOH N NaOH THF LDA 1) NaH, THF EtO THF-78 °C 2) CH3CH2Br heat HO CH3COOH KOH CH3NH2 KOH MeOH 1) NaOMe, MeOH 1) HCI, H20 OH 2) PhCH2Br 2) 180 °C
le
chatelier experimen
Thursday). 1. What starting material and reagents are needed for the following multi-step synthesis (HINT: aldol reactions work best when the starting material can only form one enolate)? 5 он о D. NaOH, H2O, Heat F. HO E. NaOH, H2O G. LDA Starting Material: Reagents: 2. LDA is a strong, sterically hindered base and will form the enolate. Sodium hydride is a weak base and will form the _ - enolate. Kinetic enolates are the stable and...
(more synthesis, continued. 2 points each) 2 Bra 2 NaOH Ph water g. 1. LDA 1. NaOCHs CHOH 2. BrCH CH2CHs 3. H', H20, heat H Ph (warmup, long time) NaOEt k. OEt EtOH 1. PPhs Br 2. BuLi 3.
28 - Fill in the hal ini tersing a 08 - Fill in the boxes with the product(s) for the following reactions. Draw only the predominate regioisomer and indicate the stereochemistry where appropriate. If a racemic mixture is formed, you may indicate this using a wavy line or mark the chiral center with an asterisk (*), and write racemic in the box. 1) NaOPr, ProH 2) H307 1) NaoMe, MeOH OMe 2) H30+ 1) LDA (1.1 eq) 2) OEt 3)...
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