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1) Which product will be created by these reactions: i ) je te si are Å...
10. Select the compound that can not be made using the malonic ester synthesis: O O...
10. Select the compound that can not be made using the malonic ester synthesis: O O OH MeO Оме OH Ph OH A. B. Ph C. D. 11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A. the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel D....
11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid...
11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel D. this generates heat leading to decarboxylation 0 12. Select the proper sequence of reactions needed to produce the desired final product: ? A. NaoMe, Mel/NaOMe, allyl-Br /...
10. Select the compound that can not be made using the malonic ester synthesis: O o...
10. Select the compound that can not be made using the malonic ester synthesis: O o O OH MeO OMe OH Ph ОН A. B. Ph C. D. 11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A. the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel...
11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid...
11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? C. the ionized cation partitions to the aqueous layer A. the alkoxy cation needs to be eliminated in the separatory funnel B. the stabilized enolate adds a proton D. this generates heat leading to decarboxylation 14. Which reagent(s) is(are) needed to complete the desired synthesis?: O ? A. NaOM, H Meo Н. I dil. HCI B....
9. Select the product for the reaction depicted below: LDA / EtBr بل من C, A,...
9. Select the product for the reaction depicted below: LDA / EtBr بل من C, A, B. 10. Select the compound that can not be made using the malonic ester synthesis: 0 0 0 CH OMe Meo بد CH Ph CH A, B, C, Ph D,
26. Select the product for the transformation indicated: CO Me COMO Meo OME NaoMe MOH CO,...
26. Select the product for the transformation indicated: CO Me COMO Meo OME NaoMe MOH CO, Me 7 dil HCI ? OH CO, Me A. C D B. 27. Select the needed sequence of reactions to load from the starting material to the desired product: OH 0 OH A. PCC / Nah, MeOH / LDA, acetaldehyde / dil. HCI ? B. H.CrO4/LDA, Mel / LDA. propanal i dil. HCI C. MCPBA / Nah, MeBr / Nah, propyl-1/KOH D. NBS /...
4. Synthesis Reactions. Draw the feature product of the following reactions. (8 x 3 pts) 1....
4. Synthesis Reactions. Draw the feature product of the following reactions. (8 x 3 pts) 1. Mg Ph Br 2. CO2 3. H a "NH2 Ph 1. NaOH, CI 2. LAIH b. CHỊCH NHA NaBHgCN, H+ Ph C. Br (excess) NH d NaOH H HO OH H CH e. 1. NaOH H2O NH 2. H+ o= 1. NaOH H2O 2. SOCI N(CH3)2 3 HO
Thank you！ 9. What would be the product of the following conversion? 1. NaOEt, EIOH OEt...
Thank you！
9. What would be the product of the following conversion? 1. NaOEt, EIOH OEt 2. H,о- OEt ОН О OEt OEt OEt OE OEt e. d. 10. What is the product of the Dieckmann condensation of the following diester? 1.NaOCH, CH,Oн HgCOoc coOCHs 2. H,0* осн, COOCH COOCH b. d. both a) and b) e. a), b), and c) a. C. 11. Consider the synthesis below. What is compound X? COOEt COOH 1. КОВи 1. NAOH, H2O, heat...
no explanation needed, I just need the right answer choices. Thank you!! Predict the major organic...
no explanation needed, I just need the right answer choices.
Thank you!!
Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry. Me Me 1. Mgº, THE o Br Me H Me 1 Me 3. H20, HCI Me Y Me Me Me Me Me Me Me HO он Me Me Me Me Predict the major...
practice questions ③ show the product on products Expected for the reactions below a) + CH₃OH...
practice questions
③ show the product on products Expected for the reactions below a) + CH₃OH alcohol c-c-c aldehyde c-c-c acid C b) 014 + CH3 CH alcohol ÖH c) -10 kmnog LOH heat (Excess) cox - Bonus! 0: CEN: d) -10- H₂ Pd/c. (Excess H2) (Red) H -Bones! e) ÖH ć. + -10 alcohol он acid croch Grid x + CH₃ CH₂ 0 4 (drohol) -10 NH₂ 3 continued - show prodoct (s) رخ دن 2) 15 PH:10 NaOH...
10. Select the compound that can not be made using the malonic ester synthesis: O O OH MeO Оме OH Ph OH A. B. Ph C. D. 11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A. the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel D....
11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel D. this generates heat leading to decarboxylation 0 12. Select the proper sequence of reactions needed to produce the desired final product: ? A. NaoMe, Mel/NaOMe, allyl-Br /...
10. Select the compound that can not be made using the malonic ester synthesis: O o O OH MeO OMe OH Ph ОН A. B. Ph C. D. 11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? A. the alkoxy cation needs to be eliminated C. the ionized cation partitions to the aqueous layer B. the stabilized enolate adds a proton in the separatory funnel...
11. In general both the malonic ester and acetoacetate synthesis require the addition of dilute acid in order to generate the final product. Why? C. the ionized cation partitions to the aqueous layer A. the alkoxy cation needs to be eliminated in the separatory funnel B. the stabilized enolate adds a proton D. this generates heat leading to decarboxylation 14. Which reagent(s) is(are) needed to complete the desired synthesis?: O ? A. NaOM, H Meo Н. I dil. HCI B....
9. Select the product for the reaction depicted below: LDA / EtBr بل من C, A, B. 10. Select the compound that can not be made using the malonic ester synthesis: 0 0 0 CH OMe Meo بد CH Ph CH A, B, C, Ph D,
26. Select the product for the transformation indicated: CO Me COMO Meo OME NaoMe MOH CO, Me 7 dil HCI ? OH CO, Me A. C D B. 27. Select the needed sequence of reactions to load from the starting material to the desired product: OH 0 OH A. PCC / Nah, MeOH / LDA, acetaldehyde / dil. HCI ? B. H.CrO4/LDA, Mel / LDA. propanal i dil. HCI C. MCPBA / Nah, MeBr / Nah, propyl-1/KOH D. NBS /...
4. Synthesis Reactions. Draw the feature product of the following reactions. (8 x 3 pts) 1. Mg Ph Br 2. CO2 3. H a "NH2 Ph 1. NaOH, CI 2. LAIH b. CHỊCH NHA NaBHgCN, H+ Ph C. Br (excess) NH d NaOH H HO OH H CH e. 1. NaOH H2O NH 2. H+ o= 1. NaOH H2O 2. SOCI N(CH3)2 3 HO
Thank you！
9. What would be the product of the following conversion? 1. NaOEt, EIOH OEt 2. H,о- OEt ОН О OEt OEt OEt OE OEt e. d. 10. What is the product of the Dieckmann condensation of the following diester? 1.NaOCH, CH,Oн HgCOoc coOCHs 2. H,0* осн, COOCH COOCH b. d. both a) and b) e. a), b), and c) a. C. 11. Consider the synthesis below. What is compound X? COOEt COOH 1. КОВи 1. NAOH, H2O, heat...
no explanation needed, I just need the right answer choices.
Thank you!!
Predict the major organic product of the following reactions. Assume one equivalent of reagent unless otherwise stated, it's a solvent, oxidizing, or reducing agent. If no reaction will occur, choose E. Be mindful of stereochemistry. Me Me 1. Mgº, THE o Br Me H Me 1 Me 3. H20, HCI Me Y Me Me Me Me Me Me Me HO он Me Me Me Me Predict the major...
practice questions
③ show the product on products Expected for the reactions below a) + CH₃OH alcohol c-c-c aldehyde c-c-c acid C b) 014 + CH3 CH alcohol ÖH c) -10 kmnog LOH heat (Excess) cox - Bonus! 0: CEN: d) -10- H₂ Pd/c. (Excess H2) (Red) H -Bones! e) ÖH ć. + -10 alcohol он acid croch Grid x + CH₃ CH₂ 0 4 (drohol) -10 NH₂ 3 continued - show prodoct (s) رخ دن 2) 15 PH:10 NaOH...
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