3. The final product is removed from the organic layer by extraction with the hydrochloric acid solution. Draw the curved arrows for the proton transfer reaction that takes place, and draw the resulting product. Explain how this reaction enables the removal of the lidocaine from the organic layers. H + H-CI
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- mheducation.com/ext/map/index.html?_con=con&external_browser=D0&launchUrl=https%253A%252F%252Fcompass2g.illinois.edu%252Fweb wing i Saved Complete the reactions to show the synthesis of the following compound from (CH,),CHCH,CH,Br. Part 1: Br K OC(CH3)3 view structure Part 2 out of 2 Br2 H,O What reagent is needed where the "?" is located?The final step in the synthesis of morphine (shown) is an organic solvent extraction to purify morphine from unconsumed reactants. Morphine has two weak acid alcohol groups with pks of 10.0. Before the organic extraction can take place, the pH of the solution must be adjusted to maximize the organic solubility of the morphine. Choose HO the pH range that would result in the highest recovery of morphine. H H- N-CH3 HO a) pH 9 - 10 b) pH 7 - 8 с) рH 11 - 12 d) pH 13 - 14Acetic acid was also formed in the synthesis of aspirin and would be present with aspirin in the reaction mbrture. Why is it unlikely that your isolated aspirin is contaminated with acetic acid? a Whet le voun euld*(f) 1. xs 1. i-PrMgBr - abbreviation 6 2. H20 2. H20 Isopropyl 4-oxo- pentanoate Excess isoprору! magnesium bromide followed by water1. To pass Chem 18.1, ELIBAP must be able to determine the melting points of three ester compounds extracted and purified from three different plants. Ester 1 Ester 2 Ester 3 :0: H. MW: 182.17 g/mol MW: 152.15 g/mol MW: 164.20 g/mol Possible Melting Points: -31 °C 64-67 °C -9 °C a. Given the molar mass and molecular structures of the esters, determine their most possible melting points. b. According to her friend who took Chem 18.1 last semester, one of the ester compounds exists as a solid above room temperature (25 °C) while the rest remain in their liquid forms. Identify the ester which is present in solid form above room temperature. Draw the structure.Cs Scanned with CamScanner 15. Give the step-by-step mechanism using curved arrows for the following reaction. Comment on why base catalysis is unsuitable for this reaction. LHO CO,H CO2Et HD. OXIDATION OF ALCOHOLS1. Place 1 mL of each of the following alcohols in separate clean test tubes: ethanol,benzyl alcohol and ethylene glycol.2. To each alcohol sample, add 2 mL of acidified potassium dichromate solution.Mix by shaking gently and observe any changes. Warm gently if necessary to startthe reaction.Record results in the table below.Alcohol Color changes observed Ethyl AlcoholBenzyl AlcoholGlycerol Equations for the oxidation of each alcohol:a. _________________________________________________________________b. _________________________________________________________________c. _________________________________________________________________E. FORMATION OF ESTERS1. To 2 mL of ethyl alcohol, add 1 mL of glacial acetic acid and 2 drops ofconcentrated sulfuric acid (CAUTION). Warm gently, then pour into a beakercontaining 20 mL of ice water previously made alkaline with sodium carbonatesolution. Stir well and note the…Provide the major organic product for the 1. LilH 4 2.нсін, о Provide the major organic product of the following reaction. following reaction. ?. 6. Provide the major organic product for the following reaction. HO Br OH NH - Br 1. LIAIH4 2. HC1, H₂O 7. Provide the major organic product of the following reaction. concentrated KMnO4 reflux1. Complete the following flowchart. H₂N Aqueous phase Add NaOH pellets OH OH + 1) Dissolved in ether 2) Extracted w/ 3M HCI Aqueous phase Add conc. HCI Organic phase Extracted w/ 3M NaOH Organic phase6) What is the nucleophilic site in the following compounds? H3C-0-CH3 H2C=CH2 CH;NH2 II II A) | = Hydrogen; I| = TT electrons in bond; III = nitrogen. %3D B) | = Oxygen; II = carbon; III = nitrogen. C) Hydrogen; II = carbon; III = carbon. %3D D) | = Oxygen; II = TT electrons in bond; III = nitrogen.0&launchUrl=https%253A%252F%252Fcompass2g.illinois.edu%252Fwebapps%252Fpc rawing i Saved Help Be sure to answer all parts. Complete the reactions to show the synthesis of the following compound from (CH3),CHCH,CH,Br. Part 1 out of 2 Br K OC(CHak Hint draw structure Solution Next part Guided Solution *******NN*****ghan Currie Yo... Yin Yoga For The... 2 Workouts | Athleti... M Gmail D2L Homepage - Sum... D2L Homepage - Sum... Question 8 of 14 ZI 5th_grade_studen... Charred Red Cabb... The organic product of the reduction of the compound shown is A) ammonia B) primary amine C) secondary amine D) tertiary amine E) ammonium ion Menu-Simone's...SEE MORE QUESTIONS