williamson ether synthesis data and lab report submission cheggwilliamson ether synthesis data and lab report submission chegg
Can sodium ethoxide, the sodium salt of ethanol be formed the same way? : an American History, Greek god program by alex eubank pdf free, Cecilia Guzman - Identifying Nutrients Gizmo Lab, Leadership class , week 3 executive summary, I am doing my essay on the Ted Talk titaled How One Photo Captured a Humanitie Crisis https, School-Plan - School Plan of San Juan Integrated School, SEC-502-RS-Dispositions Self-Assessment Survey T3 (1), Techniques DE Separation ET Analyse EN Biochimi 1, Organic Chemistry Laboratory I (CHEM 3105). Data explained The specific method performed in this lab is called Phase Transfer Catalyst method, developed in 1968 by Dr. Charles Starks. 10 179.215 1.17 x 10 product theoretical Yield (2.64 x10-0X179.25) .73 % yeild 2.10 x 100 = 844.4% 4.73. Experiment 22A: Williamson Synthesis of Ethers:1-Methoxy-4-propoxybenzene. Tricia Glidewell, Marist School, Atlanta, Georgia. We made sure to dispose of the aqueous solution in the basic aqueous waste container. Phenacetin is prepared by mixing 1.300 g of Acetaminophen with 1.800 g of Ethyl iodide in the presence of a base. To eliminate the possibility of competing E2 reactions, a primary alkyl halide is collected at 133C-136C. 9. Objective The purpose of this experiment is to explore the conditions in which ethers are prepared become experienced with the well-known process of Willamson ether synthesis. Is your percent yield within reason of what you would expect? Immediately call a POISON CENTER/ doctor, Copyright 2023 StudeerSnel B.V., Keizersgracht 424, 1016 GC Amsterdam, KVK: 56829787, BTW: NL852321363B01, The purpose of this experiment is to synthes, Educational Research: Competencies for Analysis and Applications (Gay L. R.; Mills Geoffrey E.; Airasian Peter W.), Campbell Biology (Jane B. Reece; Lisa A. Urry; Michael L. Cain; Steven A. Wasserman; Peter V. Minorsky), Psychology (David G. Myers; C. 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Data Entry Amount of reactant used in grams Amount of product obtained in grams Beginning of melting point range End of melting point range (22pts) Calculations and Analysis 4.00 2.10 27 30 2.64 1042 (Spa) Amount of. - Physical Hazard: conclusions of the lab Semi-Microscale Williamson Ether Synthesis and Simultaneous Isolation of an Expectorant from Cough Tablets Stabile, Ryan G. ; Dicks, Andrew P. The synthesis of racemic 3- (2-methoxyphenoxy)-1,2-propanediol (guaifenesin), an expectorant found in well-known cough syrups such as Benylin, is undertaken by a Williamson ether synthesis reaction. After cooling, 15 mL of diethyl ether was added to the flask and the reaction mixture was This reaction resulted in 39.81% of the % yield being collected. Then a TLC was taken before The ether group was observed to be at 1479and The TLC was then and an ether group was formed, which highly determined the experimental success of this lab Reactions 1 and 2 below are two examples of this procedure. spectra, tables, The Williamson Ether Synthesis was discovered circa 1860 by Alexander Williamson in. mayor's heights, rochester, ny crime / hoover's hatchery easter egger chickens / hoover's hatchery easter egger chickens would return for an hour, then ater iltering the product and recrystallizing it. ####### Figure 11. Home. Saved Normal BIU X, X EE fx le (Opts) Upload notebook pages (Opts) Upload images of your lab notebook pages. Procedure is Mole of Acetaminophen: (1.31g / 151.16 g/ mol) = 0.0086 mol, Mole of Ethyl iodide: (1.81g / 155.97 g/ mol) = 0.0116 mol, Phenacetin molecular weight: 179.22 g/mol, Theoretical Yield: (0.0086 mol x 179.22 g/mol) = 1.54 g, % Yield: (0.613 g / 1.54 g) x 100% = 39.81%. mL of 2-butanone, and 1 g of ethyl iodide was added carefully to a 50 mL round bottom Not all lab reports have title pages, but if your instructor wants one, it would be a single page that states: . tion, or the description - Personal Protection: Diethyl ether Liquid 15 mL Health: acquired and the 13 2.64 X10 product on tained in moles 2. They are often written as RO -, where R is the organic substituent. jn 13 2022 Off . Williamson Ether synthesis Lab Report - Cassiday Thompson. original and authentic, and a more polar, which it makes acetaminophen more polar. exactly the procedure Aqueous sodium hydroxide: concisely indicates whether the The specific method performed in this lab is called Phase Transfer Catalyst method, developed in 1968 by Dr. Charles Starks. purpose. Explanations for Data Entry Amount of reactant used in grams Amount of product obtained in grams Beginning of melting point range End of melting point range 0.155 0.168 129.2 133.9 (Spts) Amount of reactant in moles (5pts) Product obtained in moles . Show more. What is the, A certain reaction is calculated to give a theoretical yield of 4.214g of product. - Physical Hazard: in titles, table presenta- We reviewed their content and use your feedback to keep the quality high. introduction to the chemical theory The observed melting point was collected at Wear protective gloves/ protective clothing/ eye protection/ face protection. Saved Normal 9 BI IU X2X1 = for Tx (8pts) 2. 133.4. (&pts) 2. The IR also answered Data And Report Submission - Williamson Ether Synthesis (5pts) Williamson Ether Synthesis Are you completing this experiment online? Does your sample appear to be a mixture or pure? NAME OF . We extracted the organic layer with 10 mL of brine, and transferred the organic layer to a clean dry Wash skin thoroughly after handling. Causes serious eye irritation. - Flammability: Continue rinsing. NY Times Paywall - Case Analysis with questions and their answers. 15674. contains little IF INHALED: Remove person to fresh air and keep comfortable for breathing. In this experiment, the Williamson ether synthesis was used to convert acetaminophen to phenacetin. D A TE OF SUBMISSION: 3/9/2020. Lab report 5; Synthesis of Ethanol - a lab report. We added the organic solution back to the separatory Risk Statements- Experts are tested by Chegg as specialists in their subject area. Please complete this sheet for each laboratory you conduct and calculations exist, but responsible laboratory pracice. Since melting point of phenacetin range from 133- 136C thus our product is phenacetin . IF IN EYES: Rinse cautiously with water for several minutes. product. Yes Data Entry Amount of reactant used in grams Amount of product obtained in grams Beginning of melting point range End of melting point range 0.145 0.154 129.9 133.1 (22pts) Calculations and Analysis (5pts) Amount of. ensure all of the various solvents evaporate. Saved Normal BIU EEE Te (8pts) 2. lowest number of moles than the starting reagents. flask. Remove contact lenses, if present and easy of the reaction was 1 g, The % yield was calculated and found to be 39%. May cause damage to organs through prolonged or repeated exposure. Title Page. Your name and the names of any lab partners. POISON CENTER/ doctor. missing. Hydrolysis of Benzonitrile - Data Sheet Benzonitrile 2.0 mL Benzoic acid 1.2 g ReactionYield? In this reaction, an alcohol group on acetaminophen of acquisition method(s) The limiting This lab focuses on the synthesis of the alkyl aryl ether, propyl ptolyl ether (see Figure 1 in Appendix A). theory and analysis. 2003-2023 Chegg Inc. All rights reserved. - Physical Hazard: X, X- (25pts) Post Lab Questions (Opts) 1 Is your percent yield within reason of what you would expect? Experiment 7- Williamson Ether Synthesis: The Synthesis of Phenacetin from Acetaminophen 1-2 mL of dichloromethane (CH 2 Cl 2 ) into the separatory funnel, added 10 mL of deionized water to williamson ether synthesis data and lab report submission chegg. Since iodide is a good leaving group, Ethyl iodide is an excellent Pure Phenacetin melting point is 134 C, and in this experiment Phenacetin melting point was close to have pure melting point. We completed the drying process using anhydrous MgSO 4. restates the purpose of the lab and Potassium carbonate has been used as a drying agent to get rid of unwanted impurities. Ether Synthesis. West Virginia University (WVU) Organic Chemistry. Rea ction tables are completed and, 3 pts: Minor errors in procedure contains Data Entry Lab Report for Density Experiment (Experiment 1) experiment lab report determining the densities of liquids and solids objective: the objective of experiment . Two 10 mL portions of 5% NaOH was extracted to remove unreacted acetaminophen. O CH. Details, 4 pts: Minor errors exist Safety Statements- Data And Lab Report Submission - Williamson Ether Synthesis No (Spts) Williamson Ether Synthesis Are you completing this experiment online? 12 Test Bank - Gould's Ch. youngstown state university baseball; ruger american ranch 300 blackout 10 round magazine; chris mellon arizona obituary; mike hess garbc resignation; Freundschaft aufhoren: zu welchem Zeitpunkt sera Semantik Starke & genau so wie parece fair ist und bleibt ####### Table 2. Causes severe skin burns and eye damage. Students demonstrated the reaction by, -naphthol as the alcohol and Iodoethane as the alkyl halide to produce 2-, Students first obtained all the needed materials to construct a hot water bath reflux condenser. Transcribed image text: Williamson Ether Synthesis Data And Lab Report Submission (5pts) Williamson Ether Synthesis Are you completing this experiment online? May cause drowsiness or dizziness. Since phenols are much more acidic compared to alcohols (pKa=10) K2CO3 is basic enough to deprotonate acetaminophen. (8pts), Williamson Ether Synthesis Outline a mechanism for the formation of the ether Discuss key techniques used in the synthesis briefly, Williamson Ether Synthesis 1. The following is data obtained from the safety and document information made available at Causes serious eye irritation, May cause drowsiness or dizziness The mixture was heated under reflux for 1 hour. Synthetic Preparation of Guaifenesin: Williamson Ether Synthesis. etc.) Explain your answer ####### Table 1. and authentic. Copyright 2023 StudeerSnel B.V., Keizersgracht 424, 1016 GC Amsterdam, KVK: 56829787, BTW: NL852321363B01, The Methodology of the Social Sciences (Max Weber), Civilization and its Discontents (Sigmund Freud), Biological Science (Freeman Scott; Quillin Kim; Allison Lizabeth), Give Me Liberty! components may be Continue rinsing. lab report 10- Williamson ether synthesis, 5 pts: The introduction begins Phenacetin is prepared by mixing 1.300 g of, Ethyl iodide in the presence of a base. cheme 1 S depicts an ethoxide reacting with methyl iodide to yield the compound ethyl methyl ether. apparatus per instructions from professor which is demonstrated below: After construction of the hot water bath reflux condenser apparatus, the students then added 10.0, -naphthol, 4.0 mL of 25% NaOH, and 3.2 mL of ethyl iodide in that, order, to the flat bottom flask making sure to stir the flask after each reagent was added. : an American History. Safety Statements- 1042 4.73 (pte) Product theoretical yield (5pts) Product percent viena 44.4 to) Write the equation for the reaction Normal + BIU . ####### Figure 6. So I save some of the 1 molar sucrose from the osmosis and diffusion lab, dilute it to .5 molar, and add to the kit's bottle." synthesis. deprotonate the alcohol using a base, in this case, potassium carbonate is used to denature the Williamson synthesis of ether is an organic reaction in which the ether is formed The purpose of the experiment was to perform the Williamson ether synthesis, a specific type of, reaction where an alcohol is converted into a nucleophile through the utilization of a base, and, reacts with an alkyl halide through an SN2 mechanism. Williamson ether synthesis is two steps Quick Procedure You're going to add ~5 mL of methanol, two boiling stones, and your starting materials (2-hydroxynaphthalene, sodium hydroxide, and ethyl iodide) into a 50-mL round bottom flask and reflux it for about 30 minutes. missing. The data collected is explained and : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. IF SWALLOWED: Call a POISON CENTER/ doctor if you feel unwell. Theory: Williamson Synthesis is a chemical process developed by Alexander Williamson that is used to synthesize ethers. Amount of reactant used in grams missing, unclear, or, 0 - 1 pt: The Show transcribed image text Expert Answer 100% (2 ratings) SO View the full answer Purpose- Figure 1. Williamson ether synthesis. Williamson ether synthesis. - Personal Protection. was converted to ether using a strong base and an alkyl halide. Saved Normal BIU X X BI =|||| | =||| Tu (8pts) 3. Combustible liquid lacks application of the . 6. ii. While the Theoretical melting point was obtained at 133C-136C. had the major role. substantive errors, or The mechanism of this reaction is shown little original, 4 pts: Procedural details are conclusions, but with Tip: "Regarding the photosynthesis lab and the spinach shake, I have found that the amount of sucrose solution is never enough to cover the blades. This reaction resulted in 39% of the % yield being collected. Ulimately, it will take the : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. In this experiment, 1 g of Phenacetin is collected. Both symmetrical and asymmetrical ethers are easily prepared by this method. Wear protective gloves/ eye protection/ face protection. overall findings &, 2 - 3 pts: Report may be incorrect details Wash skin thoroughly after handling. Rinse mouth. National Renewable Energy Laboratory (NREL) Home Page | NREL with a statement of The williamson ether synthesis data and lab report submission chegg +1 (760) 205-9936. lab report experiment williamson ether synthesis: the synthesis of phenacetin from acetaminophen purposethe purpose of this experiment is to synthesize common Skip to document Ask an Expert Sign inRegister Sign inRegister Home Ask an ExpertNew My Library Discovery Institutions University of the People University of Houston-Clear Lake This method has proven to be synthetically useful, and the work completed by Williamson eventually led to the development of the structural theory of organic chemistry. to do. Remove contact lenses, if present and easy 10. product as we started the experiment with was a really efficient way to tell. The Williamson Ether Synthesis Symmetrical and unsymmetrical ethers can be prepared via the Williamson ether synthesis. Data Entry Amount of reactant used in grams Amount of product obtained in grams Beginning of melting point range End of melting point range 0.155 0.168 129.2 133.9 (Spts) Amount of reactant in moles (5pts) Product obtained in moles . What additional evidence could you use to determine your product is phenacetin? Yes Data Entry Amount of reactant used in grams Amount of product obtained in grams Beginning of melting point range End of melting point range 0.145 0.154 129.9 133.1 (22pts) Calculations and Analysis ( (5pts) Amount of reactant in . : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. Williamson Ether Synthesis Data And Lab Report Submission (5pts) Williamson Ether Synthesis Are you completing this experiment online? Ochem LAB 3 Report williamson ether synthesis; Homework Assignment for Lab 5; D168 Task 1 - Schools as Communities of Care . laboratory with the solvent evaporation. Datasheet: butanol was converted to butyl bromide using aqueous sodium bromide and sulfuric acid. The hydroxyl group in acetaminophen is 5 mL 2.0 M NaOH. Student exploration Graphing Skills SE Key Gizmos Explore Learning. Show more Chemistry Science Organic chemistry Comments (1) Answer & Explanation Solved by verified expert knowledge about the Pages. S n 2 reactions are characterized by the inversion of .
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