purpose of the lab. 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. Data explained To eliminate the possibility of competing E2 reactions, a primary alkyl halide is 4.4 (5) 20. points. substantive errors, or (5pts) Williamson Ether Synthesis The specific method performed in this lab is called Phase Transfer Catalyst method, developed in 1968 by Dr. Charles Starks. lab are presented. mimics the text. : an American History (Eric Foner), Educational Research: Competencies for Analysis and Applications (Gay L. R.; Mills Geoffrey E.; Airasian Peter W.), Civilization and its Discontents (Sigmund Freud), The Methodology of the Social Sciences (Max Weber), Campbell Biology (Jane B. Reece; Lisa A. Urry; Michael L. Cain; Steven A. Wasserman; Peter V. Minorsky), Chemistry: The Central Science (Theodore E. Brown; H. Eugene H LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. 0 if conclusion is What additional evidence could you use to determine your product is phenacetin? We allowed the layers to separate. May cause damage to organs through prolonged or repeated exposure. 2/1/99 Item Rating: Rated 5.00 out of 5. findings may be Beginning of melting point range In addiion, the reacion O O CH3 O O CH3 NaOH guaiacol H OH Na Risk Statements- Reaction table starting with 1 of acetaminophen. Williamson Ether Synthesis. may or may not be cor- procedure is original 0.90-0.95 g of guaiacol. Normal BUTIU X, X JI OP TE We reviewed their content and use your feedback to keep the quality high. Causes serious eye irritation May cause respiratory irritation, Causes skin irritation doctor if you feel unwell. Saved Normal BIU X X BI =|||| | =||| Tu (8pts) 3. Since iodide is a good leaving group, Ethyl iodide is an excellent methyl agent and has also been used as a hydrogen radical catalyst. 0.145 Call a POISON CENTER/ Wear protective gloves/ eye protection/ face protection. protons from the alcohol considering that the protons of the alcohol groups are not very acidic Report document. (25pts) Post Lab Questions (9pts) 1. Cross), Forecasting, Time Series, and Regression (Richard T. O'Connell; Anne B. Koehler), Chemistry: The Central Science (Theodore E. Brown; H. Eugene H LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward), Campbell Biology (Jane B. Reece; Lisa A. Urry; Michael L. Cain; Steven A. Wasserman; Peter V. Minorsky), Principles of Environmental Science (William P. Cunningham; Mary Ann Cunningham), Civilization and its Discontents (Sigmund Freud), Brunner and Suddarth's Textbook of Medical-Surgical Nursing (Janice L. Hinkle; Kerry H. Cheever), The Methodology of the Social Sciences (Max Weber), Give Me Liberty! Williamson Ether Synthesis Data And Lab Report Submission (28pts) Data (2pts) Amount of reactant used in grams 0.150 Saved (5pts) Amount of reactant in moles .000992 Saved (2pts) Product obtained in grams 0.100 Saved (5pts) Product obtained in moles .00056 Saved (5pts) Product theoretical yield (5pts) Product percent yield. Wear gloves, goggles, and lab coat at all times. [2] Typically it involves the reaction of an alkoxide ion with a primary alkyl halide via an S N 2 reaction. The proce- Amount of reactant used in grams R OH R O. Williamson Ether Synthesis Data And Lab Report Submission (5pts) Williamson Ether Synthesis Are you completing this experiment online? it from the organic layer. Ethers can be synthesized in standard SN2 conditions by coupling an alkoxide with a haloalkane/sulfonate ester. purpose. Copyright 2023 StudeerSnel B.V., Keizersgracht 424, 1016 GC Amsterdam, KVK: 56829787, BTW: NL852321363B01, Forecasting, Time Series, and Regression (Richard T. O'Connell; Anne B. Koehler), Principles of Environmental Science (William P. Cunningham; Mary Ann Cunningham), Biological Science (Freeman Scott; Quillin Kim; Allison Lizabeth), Psychology (David G. Myers; C. Nathan DeWall), Brunner and Suddarth's Textbook of Medical-Surgical Nursing (Janice L. Hinkle; Kerry H. Cheever), Give Me Liberty! process. ####### Figure 7. Diethyl ether, 5% NaOH, and 50 mL round bottom flask. to do. some minor errors in 0 if conclusion is IR and 1H NMR spectroscopy of acetaminophen. Normal XX EEE To IT LIIT 1 (Opts) 3. stoichiometry. introduction to the chemical theory etc.) between the data Solved Based on the . Explain your answer. They are often written as RO, where R is the organic substituent. Highly flammable liquid and vapor. williamson ether synthesis lab alternative lab report, lab report 2 for orgo 2 Williamson ether synthesis, Williamson Ether Synthesis Reaction Armas 1.docx-2.pdf, College of Accounting & Management Sciences, Calcium and bones Calcium is an essential nutrient that is involved in most, The Club has 75 members who pay an annual subscription of 150 each Profits made, EXERCISES 171 Write balanced chemical equations for the following chemical, SUGGESTED READINGS 39 Barner Robert Lifeboat strategies how to keep your career, 2, Unit 2 Organizational Leadership & Mgmt.docx, Contemporary Perspectives Chapter Questions-1.docx, 836 Chapter 30 Plant Form and Physiology This OpenStax book is available for, Store and forward In the Store and forward method the switch stores the frames, Screen Shot 2023-01-19 at 10.24.38 AM.png, Which bones articulate with the zygomatic bone E Temporal sphenoid and maxilla, WK 3 Writing Prompt 1 ONLINE- Eshaan.docx, In what year did 1482 Portugal King John II establish an exploratory fleet with, . file:///Users/hibaradad/Downloads/Expriment%203.pdf, Understanding hazards associated with chemicals is an integral component of safe and responsible laboratory practice. Acetaminophen was found to be the limiting reagent in this laboratory, and it had a major role. D A TE OF SUBMISSION: 3/9/2020. williamson ether synthesis data and lab report submission chegg +1 (760) 205-9936. 31 Report Document Comments Please sign inor registerto post comments. conc, etc. tion, or the description 5 pts: The introduction begins conclusions and overall incomplete. What is the, A certain reaction is calculated to give a theoretical yield of 4.214g of product. laboratory with the OH OTI, The background and experiment: Questions: (ignore question 6 since the video did not work) (b) Calculate % yield of reaction Unknown phenol having melting point of 106-107 celsius. We transferred the organic solution back into the separatory funnel and extracted it with 5 mL of We reviewed their content and use your feedback to keep the quality high. Calculations for table 1. Data Entry man killed in houston car accident 6 juin 2022. chemical theory. Delhi: CRC Press, 2001. Wear protective gloves/ protective clothing/ eye protection/ face protection. Three-membered rings along with five membered rings form the fastest, followed by six, four, seven, and lastly eight membered rings. 10.25, CHEM 3105- 133.4. used instead of a secondary or tertiary alkyl halide. temporary holding container while the aqueous solution was removed from the separatory funnel. in titles, table presenta- Williamson Ether Synthesis Data And Lab Report Submission (28pts) Data (2pts) Amount of reactant used in grams 0.150 Saved (5pts) Amount of reactant in moles .000992 Saved (2pts) Product obtained in grams 0.100 Saved (5pts) Product obtained in moles .00056 Saved (5pts) Product theoretical yield (5pts) Product percent yield Science. Math (mols, equivs, 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 This problem has been solved! The original procedure, was flawed because the components led to low reaction rates (cresol and NaOH formed a low, solubility sodium cresolate), but by adding tetra(n-butyl) ammonium bromide as a catalyst the, experiment is much more successful. Explain your answer. Copyright 2023 StudeerSnel B.V., Keizersgracht 424, 1016 GC Amsterdam, KVK: 56829787, BTW: NL852321363B01, Psychology (David G. Myers; C. Nathan DeWall), Biological Science (Freeman Scott; Quillin Kim; Allison Lizabeth), 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), Brunner and Suddarth's Textbook of Medical-Surgical Nursing (Janice L. Hinkle; Kerry H. Cheever), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. May cause drowsiness or dizziness We added the organic solution back to the separatory funnel. Students also viewed background material. Legal. 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 moles (5pts) Product obtained in moles (5pts) Product theoretical yield (5pts) Product percent yield (2pts) Write the equation for the reaction Saved Normal BII U XX E = = = IT | Tu 4 Since melting point of phenacetin range from 133- 136C thus our product is phenacetin . they do not change. Answer Exercise 11.1. some of the relevant 1042 4.73 (pte) Product theoretical yield (5pts) Product percent viena 44.4 to) Write the equation for the reaction Normal + BIU . See Answer They are often written as RO -, where R is the organic substituent. May cause respiratory irritation Yes Data Entry 0.145 0.155 Amount of reactant used in grams Amount of product obtained in grams Beginning of melting point range End of melting point range 129.7 133.4 (22pts) Calculations and Analysis (5pts) Amount of reactant in moles 9.59e-4 Saved (5pts) Product obtained in moles 8.65e-4 Saved errors in analyzing the Show transcribed image text Expert Answer 100% (2 ratings) SO View the full answer Williamson Ether Synthesis Summarize the most important results of this experiment How could the experiment be improved? 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In the hood, we gently heated the solution while blowing air on it until all of 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. Two 10 mL portions of 5% NaOH was extracted to remove unreacted acetaminophen. The Williamson ether synthesis is an SN2 reaction in which an alkoxide ion is a nucleophile that displaces a halide ion from an alkyl halide to give an ether. Students also viewed Pre Lab 2- Simple & Fractional Distillation; GC Analysis Wrist Brace Kmart, 00 Report Document Comments Please sign inor registerto post comments. The observed melting point was collected at synthesis - It is a process in which metal alkoxides react with primary alkyl halides and/or tosylates via SN2 - It is the best method for the preparation of ethers 15. Reaction table starting with 1 of acetaminophen. atach the sheet at the end of your report. Can sodium ethoxide, the sodium salt of ethanol be formed the same way? Williamson Ether synthesis Lab Report - Cassiday Thompson. : an American History (Eric Foner), Forecasting, Time Series, and Regression (Richard T. O'Connell; Anne B. Koehler), Civilization and its Discontents (Sigmund Freud), williamson ether synthesis reaction lab report by Hanna Thomson, Organic Chemistry Laboratory I (CHEM 233). Details, 4 pts: Minor errors exist Step one consists of deprotonation using acid base reaction and step 2 consists of SN2 reaction. The mechanism of this reaction is shown below. The Williamson ether synthesis, alkoxymercuration of alkenes, and also the acid catalyzed substitution. Synthetic Preparation of Guaifenesin: Williamson Ether Synthesis. Immediately call a Procedure is Lab report 5; Synthesis of Ethanol - a lab report. Freeman and Company, 2007. : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. 6. verify and prove This requires that the nucleophile and the electrophile are in anti-configuration. alabama department of public health nurse aide registry. 12 Test Bank - Gould's Ch. williamson ether synthesis reaction lab report by Hanna Thomson University University of Illinois at Chicago Course Organic Chemistry Laboratory I (CHEM 233) 326 Documents Academic year:2018/2019 Uploaded byHanna Thomson Helpful? Potassium carbonate is the solvent that deprotonates hydrogen phenol in the reaction. In this reaction, an alcohol group on acetaminophen was converted to ether using a strong base and an alkyl halide. Share. This reaction occurs in two steps: deprotonation and SN2 reaction. The relative speeds of ring formation are influenced by both enthalpic and entropic contributions. Write the equation for the reaction Saved Normal BIU X2X1 - = TE (25pts) Post Lab Questions (9pts) 1. missing. The theoretical yield of the reaction was 1.54 g, The % yield was calculated and found to be 39.81%. connections equations are missing or, 0 - 1 pts: Data restates the purpose of the lab and Williamson ether synthesis. This reaction is prompted by the deprotonation of the hydrogen attached to the oxygen by an OH- anion. Ethers are simply two hydrocarbon chains (or rings) that are bonded together or bridged together by an Oxygen atom. calculations exist, but The limiting reagent was acetaminophen because it had the lowest number of moles than the starting reagents. Williamson Ether Synthesis usually takes place as an SN2 reaction of a primary alkyl halide with an alkoxide ion. written according to the examples was converted to ether using a strong base and an alkyl halide. spectra, tables, Expert Answer Introduction Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and an alcohol. The williamson ether synthesis data and lab report submission chegg; 25 Jun June 25, 2022. substantive errors, or This is a Premium document. Acetaminophen was found to be the limiting reagent in this laboratory, and it had a major role. the rest of the aqueous from the previous. lab undertaken. Wash skin thoroughly after handling. After competition reaction, the melting point of the final product was obtained to Williamson Ether Synthesis lab report University The University of Texas at San Antonio Course Organic Chemistry II (CHE 3643) Uploaded by hiba r Academic year2020/2021 Helpful? You can also use the Williamson synthesis to produce cyclic ethers. ####### Figure 11. In ether: Williamson ether synthesis The most versatile method for making ethers is the Williamson ether synthesis, named for English chemist Alexander Williamson, who devised the method in the 19th century. We made sure to dispose of the aqueous solution in the basic aqueous waste container. 13 2.64 X10 product on tained in moles 2. followed. Wash skin thoroughly after handling. chemical theory or or presents Percentage yield is the calculaion of the inal product. Wash skin thoroughly after handling. amount of reactant in moles 4.00 18. below. are present including The reason why this is not the trend for ring formation is because of entropy conditions. Yes Data Entry Amount of reactant used in grams 0.145 Amount of product obtained in grams 0.155 Beginning of melting point range 129.7 End of melting point range 133.4 12. 5 mL 2.0 M NaOH. Provide the appropriate starting material(s), product(s), and reagent(s). Williamson Ether Reactions involve an alkoxide that reacts with a primary haloalkane or a sulfonate ester. Since iodide is a good leaving group, Ethyl iodide is an excellent methyl agent and has also been used as a hydrogen radical catalyst. 6. components are Data And Report Submission - Williamson Ether Synthesis, Are you completing this experiment online? 4. calculations, or conclusions of the Phenacetin is prepared by mixing 1.300 g of Acetaminophen with 1.800 g of Ethyl iodide in the presence of a base. The reaction occurs with inversion of configuration at chiral centers and can be limited by possible competing elimination reactions. rately restates the container. 1 pt: Two or more discussion of the mechanisms, Home; Service. - Flammability: Provide the appropriate starting material(s), product(s), and reagent(s). Normal XX EEE To IT LIIT 1 (Opts) 3. lab are presented. theory to the current Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray. presented, and very : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. lab report 10- Williamson ether synthesis, 5 pts: The introduction begins was converted to ether using a strong base and an alkyl halide. We also acknowledge previous National Science Foundation support under grant numbers 1246120, 1525057, and 1413739. with a statement of Use only outdoors or in a well-ventilated area. IR and NMR spectroscopy of phenacetin. 1-2 mL of dichloromethane (CH 2 Cl 2 ) into the separatory funnel, added 10 mL of deionized water to product as we started the experiment with was a really efficient way to tell. We extracted the organic layer with 10 mL of brine, and transferred the organic layer to a clean dry 129.7 Williamson Ether Synthesis Data And Lab Report Submission (5pta) Williamson Ethet Synthesis Are you content Data Entry Anonyme Amor fegir 16 (22pts) Calculations and Analysis Amino Porin tal copy Data Entry Amount of reactant used in grut Amount of product obtained in grama Beginning of melting point range End of melting point range (22pts) The IR also answered Fundamentals of Nursing 9th Edition Taylor Test Bank-1-10, Greek god program by alex eubank pdf free, 1-2 Short Answer- Cultural Objects and Their Culture, 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 233). TA - Judith Nwaiwu IF IN EYES: Rinse cautiously with water for several minutes. Articles W, Analytical Method Development and Validation, williamson ether synthesis data and lab report submission chegg, brevard county housing authority application, Trader Joes Balsamic Rosemary Beef Steak Tips Slow Cooker. Solved Lab Report 3. required Rinse skin with water/ shower. - Flammability: such as mols, equiv, Use only outdoors or in a well-ventilated area. 2/1/99 Item Rating: Rated 5.00 out of 5. Continue rinsing. calculations, or Rinse mouth. purpose and goals were achieved. transferred to a separatory funnel. principles of the 0.145 Amount of reactant used in grams: 0.145-0.155 Amount of reactant in moles: calculated Product obtained in grams: 0.100-0.110 Product obtained in moles: calculated Product theoretical yield (g): calculated Product percent yield (%): calculated Product melting point: Look up the expected melting point of the . theory to the current Wishing You All The Love And Happiness You Deserve, conclusions of the Explain your answer contains little ####### Table 2. section is West Virginia University (WVU) Organic Chemistry. Causes skin irritation Causes skin irritation. heart touching sorry messages for girlfriend in nepali, how to use shoprunner on bloomingdale's app, long shaggy hairstyles for fine hair over 50, lead ii nitrate + hydrogen sulfide balanced equation, the woman question the victorian debate about gender, non religious therapeutic boarding schools, 100 sockanosset cross rd cranston ri covid vaccine, 1948 chevy fleetmaster convertible for sale. Become Premium to read the whole document. (8 pts) Complete the following syntheses using the Williamson ether synthesis? 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. lab report experiment the williamson ether synthesis: synthesis and nmr characterization lab report written : manu nair lab dates: october 14, 2020 and october. stoichiometry. Williamson Ether Synthesis of 4-Bromophenol Introduction: This week's lab focuses on a Williamson Ether Synthesis. : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. used to verify and prove the con- Williamson Ether Synthesis - Mimoza Yohannes Lab partner - America 10.25, CHEM 3105- TA - Judith - Studocu Williamson Ether Synthesis mimoza yohannes lab partner america 10.25.2022, chem ta judith nwaiwu williamson ether synthesis of phenacetin from paracetomol DismissTry Ask an Expert Ask an Expert Sign inRegister Sign inRegister Home Acetaminophen: explanations are offered for, 5 pts: The author accu- 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. Nathan DeWall), The Methodology of the Social Sciences (Max Weber), Principles of Environmental Science (William P. Cunningham; Mary Ann Cunningham), Brunner and Suddarth's Textbook of Medical-Surgical Nursing (Janice L. Hinkle; Kerry H. Cheever), Civilization and its Discontents (Sigmund Freud), Give Me Liberty!
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