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could i get help on these questions? 1. NaOMe, MeOH 2. H30+ 1. NaOMe, MeOH 2....
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
Need Help. Will Rate If Complete. 1) NaoEt, EtOH Br 2) O 3) H30+ / A. 1) NaoEt, EtOH (s) ar 2) Y Br 3) Hz0+ / A 1) NaOme/MeOH ~ Br OMe 3) Hz0+/A. 1) NaOEt, EtOH 2) V Br 3) NaOEt, EtOH COOEt 5) H30+/A Robinson Annulation NaoEt, EtOH/A come lui OMe 28- The following molecules can be formed by either: Michael Reaction; Enamine Acylation; Acetoacetic Ester Synthesis; Michael Addition; Malonic Ester Synthesis; Robinson Annulation; Aldol Condensation; Claisen...
confused on these reactions 01. 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. H NaOH, H2O 3) H0 NaOH, H2O in the boxes with the products for the following reactions. Draw only the predominate copioisomer and indicate...
What product (including stereochemistry) is formed in the following intermolecular reaction? [1] NaoMe, MeOH [2] H30*
can you show the products for these claisen and crossed claisen reactions A. O 1. NaoMe 2. H30* OMe B. 1. NaOEt 2. H30 OEt C. 1. NaOEt 2. H30* Eto
2. Consider the following reaction: 1. NaOme/MeOH 2. H30* Does it have a specific name? How many products are possible? Show all of them. Suggest a synthetic route that leads to a lesser number of products. 3. Show the mechanism of formation of one of the products.
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)...
4. Predict the Product: NaBHA MeOH 1. LAH 요 2. H30* Ph3P li Php NaOEt EtOH 1. TBS-CI, imidazole ОН ОН 2. HO TsOH 1. NaOET 2. Br Br 3. NaOET 1. (1.1 equiv) LDA THF, -78°C 2. Br 1. (0.9 equiv) LDA THF, 0°C 2. Br
Provide the missing compounds and reagents in the reaction scheme below. Map at NaOMe, MeOH Select answer 1. NaOMe, MeOH 2. NaOH 3. H30*, heat Select answer NaOMe, MeOH Previous ⓧ Give Up & View Solution O Check Answer e Next Exit Hint
Hi I need help predicting the products for these reactions OEt NaOCH.CH CH,CH OH b. H, O/H,0 a. NaOCH.CH CH,CH,OH b. Br c. NaOHH O, beat d. H2O*/H2O 1. NaCN, DMSO 2. CH,MgBr, Eto 3. H.O/H,O EN 2. NaH, CH,Br chemoselective 1. a. NaOet, EtOH Br b. 2. a. NaOH/H,O, heat b. H30+/H20 CY.NECEN cy OH b. then add HC-NH2 a. NaCN, DMSO b. HO*/H,0