Br Method 1: 1) t-BUOK 2) H3O° 3) PCC 4) MeMgBr 5) H2O 6) PCC Method 2: 1) NaOH 2) PCC 3) MeMgBr 4) H2O 5) PCC Method 3: 1) Mg 2) 3) Н-0 4) РСС Method 4: 1) Mg 2) 3) H20 4) PCC
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- (A) moose the correct product. 1. NaGE, Ero 2. H₂0, A 食。 CO₂ Et -CO₂E7 (B) Coret 31. Choose the best reagents. & 4 (A) 1. LAH; H₂0 2. CHz | 3. H₂0/H+ (B) 1. NaOH, -78% 2. CH31 3. H₂0/H (C) 1. LDA, -78%℃ 2. CH31 3. H₂₂0/H+ 1. Nah, 0°C 2. CH31 3. H₂2₂0/H+* (<) Colt (D)Dtermine the reagents that can accomplish the rxn CH2OH (1) Reagent ? (2) Reagent ? C9H1202 (4) Reagent ? (3) H+ a. (1) SOC12 (2) 1-propanol; (4) PCC/pyridine b. (1) NaH, (2) acetone, (4) NABH4 c. (1) NaH, (2) epoxide (4) PCC/pyridine d. (1) Jones reagent, (2) NaH, (4) epoxideProvide the major organic product(s) that complete the following reaction equations. Please include stereochemistry (R/S, E/Z) where applicable 1) H2 Lindlars cat. 2) Cl2, DCM Me H. K 1) PBr3 pyridine 2) NaCN OH OH H2SO4 (cat.) Ме 1) H2SO4 H20 2) NaOCI CH;CO2H, 0 °C 7
- 2. In the following multistep synthesis, fill in the missing compounds in the boxes provided: ZI Dilute H3O+ 1) 1 eq. NaH 2) For H 1) 1 eq. KH 2) Mel H3O+ 1) 1 eq. EtBr 2) H30*Draw the structure of the organic product that is formed when the compound shown below is treated with the following reagents: 1) TsCl, pyridine; 2) NaCN. Interactive 3D display mode H₂Cl OH Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single beQ2) a) Write a mechanism for the following reaction. 1.NH₂OH CI N N +ZnCl₂ 2. CINCI MeCN, Reflux 2 hr NH
- A Grades for Angela Winston: CHEM-2 0 0 C ← caps lock 52 Heavy rain soon A Choose the reagent(s) that would be most likely to complete this reaction. - . S Aktiv Chemistry alt app.101edu.co E # D م Aktiv Chemistry 8888 R ه الكاكاك الكاكاك الكاك G B H N ASUS VivoBook OOOO U ل Answered: se the reagent(s) that wou Question 11 of 27 - M الشان K alt L (1586) Oldies music playing from ctrl 1.OsO. (catalytic) 2 NMO Bra HO 1. BH-THE 2 H.O., NaOH الحالات الالالالالكاك الالالال الكاك تات 1. Hg(OAC), M.O 2. NaBH., NaOH ه + enter, shiftH14.42 - Level 3 Unanswered • 3 attempts left Shown are four possible methods to form 2-pentanone from 1-bromobutane. Select the method(s) that will actually produce the desired product as the major product. 1. 2. C `Br Method 1: 1) t-BUOK 2) H3O 3) PCC 4) MeMgBr 5) H20 6) PCC Method 2: 1) NAOH 2) PCC 3) MeMgBr 4) H2O 5) PCC Method 3: 1) Mg 2) 3) H20 4) PCC Method 4: 1) Mg 2) . 3) H2O 4) PCC 3. 4. A¬Observations on the reaction of each test sample with Baeyer's reagent. Sample +/- Observations No color change, still colored violet solution Cyclohexane Naphthalene Нехane Corn oil Нeptane Ethyne|
- esc ! Dashboard 1 Draw the products and necessary reagents of the three step retrosynthetic reaction sequence shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. https://app.101edu.co 0: F1 Bwa @ 2 CH3C(=O)CI F2 AICI 3 #3 Aktiv Chemistry 3 80 F3 Select to Draw Select to Draw S4 $ 4 800 F4 27 X % Gwque commes en la mana 5 F5 Problem 20 of 20 átv MacBook Air < 6 F6 X B C D &N N- diazepam Draw all of the expected products when this compound is completely hydrolyzed in strong acid. • You do not have to consider stereochemistry. • You should include all products. If a compound is formed more than once, add another sketcher and draw it again. Alternatively, you may use the square brackets tool to add stoichiometries greater than one. • 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.From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to acetophenone (PHCOCH3) Use the minimum number of steps; in no case are more than two steps necessary. List reagents by letter in the order that they are used; example: fa. Reagents available g. а. ВНз, ТHF: then H2O2, -OH d. PhMgBr; KMNO4, H2O then H30+ e. LIAIH4; h. POCI3, pyridine b. Br2, FeBr3 then H30+ c. CH3MgBr; f. PCC, then H3 0+ CH2 Cl2