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- (lewis acid catalyst) FeCl3 он (acetone) OH (meso - hy dro benzoin) (2,2-dime thyl-4,5-1,3-dixolane) Draw the reaction scheme and mechanism here of the following reaction. Thank you!Draw the product of the reaction shown below at physiological pH (pH = 7.4). Ignore inorganic byproducts. I Toin N N H CF3CO2H Drawing Qapp.101edu.co Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. esc F1 CH3CH2CH2OH H2SO4 (cat), heat ☀ F2 80 F3 OH a F4 W Q F5 Atoms and P Draw or ta MacBook A C F6
- Draw the major nitrogen-containing organic product(s) of the reaction shown. O O HUNCHINHCHCOCH, H₂NCHCNHCHCOCH3 1. NaOH, H₂O, room temperature CH₂OH CH(OH)CH3 2. H3O* to pH 7, room temp. • Draw only the product(s) containing nitrogen. Draw products in the ionic forms obtained under the reaction conditions. . Do not include counter-ions, e.g., Na+, I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate multiple products using the sign from the drop-down menu.One of the steps in the mechanism of the above reaction as shown below. Draw the structure of all the products of this reaction. com/mm/takeAssignCourt Rotivity.do?locator assignment-take 1 pt ment Eto O Eto O 3. NaOH, H₂O, heat 4. HCI, H₂O, heat One of the steps in the mechanism of the above reaction is shown below. Draw the structure of all of the products of this reaction. O OEt O 1. Eto Na 2 Å OH You do not have to consider stereochemistry. • Draw enolate anions in their carbanion form. . You should include all products. Ôno P Ć [References) . Include counter-ions, e.g., Na, I, in your submission, but draw them in their own separate sketcher. . Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate multiple products using the + sign from the drop-down menu. ///-000- IF Previous Email InstructorThe following reaction should under go a(n) H₂C SN1 Br NaSPh DMF A/ reaction.
- Predict the product of the given reaction. оН ОН DMP (excess)Step 4: In an acid-catalyzed epoxide ring opening, the epoxide is first protonated and can then be attacked by weak nucleophiles. H HO: :Nuc Nuc Weak nucleophiles such as water and alcohols can react with the protonated epoxide. One of the main differences between base-catalyzed and acid-catalyzed epoxide ring openings is the regiochemical product expected. In an acid-catalyzed reaction, if one of the epoxide carbons is tertiary and the other primary, the nucleophile will attack at the more substituted carbon. If the epoxide is monosubstituted, the nucleophile will attack preferentially at the primary carbon vs. the secondary carbon. Which reaction will not give the indicated product? N 1. CH,CH,O 2. H₂O OH CH₂CH₂OH, H* N CH₂CH₂OH, H 1 CHICH,O 2. H₂O HO HO H- H5. Predict the major product(s) of the following reactions. If no reaction would occur, write “NR". 요이 CN OH HOEt 1) 1.05 eq. LDA 2) H Ph 3) H+, H₂O, A OEt H+, H₂O NH, Ht NH, Ht P₂O5 1) NaOH H₂O, A 2) H3O+ 1) NaOEt 2) dil. H3O+ NHMe OMe i i NH₂ i ÅH H NaBH4 EtOH 1) 1.05 eq. LDA THF, -78 °C 2) CH3CH₂Br 1) LIAIH4 Et₂O 2) H+, H₂O, A. NaCl P₂O5 1) CH3MgBr 2) H¹, H₂O Ph3P=/ NH H+
- ← Problem 4 of 20 Draw the product of the reaction shown below. Ignore inorganic byproducts. OH NAH, PhCH₂Cl DMSO Select to Edit Ω Submit Q4. Suggest a plausible arrow-pushing mechanism for the following reaction. NH N Me NH OH OH conc. HCI H₂O 110 °C, 3 h NT ΤΗ Me OH OH 76%4. Predict the product for each reaction. Note that some have two reactions. You can give the final answer or use mechanisms to arrive at the correct answer. NH₂ Ph P KCN HBr 0₂ Me₂S OH KMnO4 I j H H+ H₂O H₂O* (COCI),, DMSO Et₂N OH Ph₂P= H₂NNH₂ HO H₂O* Дон H* 'OH alm OH H₂O* H₂O* NaBH MeOH NaBH EtOH
