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9-17. Syntheses (continued): 13. 1. LDA 2. CH 14. [Hint: think alpha carbon, first.) 1) Brz/PBry...
10-18. Syntheses (continued): 14 1. LDA 2 сны 15. (Hint: think alpha carbon, first.) 1) Brz/PBry...
10-18. Syntheses (continued): 14 1. LDA 2 сны 15. (Hint: think alpha carbon, first.) 1) Brz/PBry 2) CH3NH2 OH 16. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product 17. Perform the Claisen reaction using methyl phenylacetate. (6 pts) 18. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. CO CH 1. NaOCH 2. H,0 CO.CH
13. 1. LDA 2. CHI 14. [Hint: think alpha carbon, first.] 0 1) Brz/PBrg OH 2)...
13. 1. LDA 2. CHI 14. [Hint: think alpha carbon, first.] 0 1) Brz/PBrg OH 2) CH3NH2 15. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product. (6 pts) 16. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. CO2CH3 1. NaOCH; 2. H2O .CO2CH3 17. Perform a crossed Claisen condensation reaction with methyl benzoate and cyclohexanone under...
biologi 14. [Hint: think alpha carbon, first.) 1) Brz/PBT3 2) CH3NH2 он 15. React PhCH2CHO with...
biologi 14. [Hint: think alpha carbon, first.) 1) Brz/PBT3 2) CH3NH2 он 15. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product. (6 pts) 16. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. COUCHE 1. NaOCH, 2. H,0 .COCH 17. Perform a crossed Claisen condensation reaction with methyl benzoate and cyclohexanone under basic conditions.
10-18. Syntheses (continued): 14. 1. LDA 2 оны 15. (Hint: think alpha carbon, first.) 1) Brz/Per...
10-18. Syntheses (continued): 14. 1. LDA 2 оны 15. (Hint: think alpha carbon, first.) 1) Brz/Per 29 CHẠNH OH 16. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product 17. Perform the Claisen reaction using methyl phenylacetate. (6 pts) 18. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. Cook CO.CH 1. NOCH 2. H,0
10-18. Syntheses (continued): 14 1. LDA 2 сны 15. (Hint: think alpha carbon, first.) 1) Brz/PBry 2) CH3NH2 OH 16. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product 17. Perform the Claisen reaction using methyl phenylacetate. (6 pts) 18. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. CO CH 1. NaOCH 2. H,0 CO.CH
13. 1. LDA 2. CHI 14. [Hint: think alpha carbon, first.] 0 1) Brz/PBrg OH 2) CH3NH2 15. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product. (6 pts) 16. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. CO2CH3 1. NaOCH; 2. H2O .CO2CH3 17. Perform a crossed Claisen condensation reaction with methyl benzoate and cyclohexanone under...
biologi 14. [Hint: think alpha carbon, first.) 1) Brz/PBT3 2) CH3NH2 он 15. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product. (6 pts) 16. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. COUCHE 1. NaOCH, 2. H,0 .COCH 17. Perform a crossed Claisen condensation reaction with methyl benzoate and cyclohexanone under basic conditions.
10-18. Syntheses (continued): 14. 1. LDA 2 оны 15. (Hint: think alpha carbon, first.) 1) Brz/Per 29 CHẠNH OH 16. React PhCH2CHO with hydroxide and provide its aldol-addition product. Then, apply heat to produce its final product 17. Perform the Claisen reaction using methyl phenylacetate. (6 pts) 18. React with methoxide, then heat. Be sure to show the intermediate carbanion, then the Dieckmann product. Finally, hydrolize and provide the final product. Cook CO.CH 1. NOCH 2. H,0
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