williamson ether synthesis data and lab report chegg

Chemical 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. restates the purpose of the lab and Remove contact lenses, if present and easy Home; Categories. May cause drowsiness or dizziness. Explain your answer copied from a, "#$%&'() %+&,)--)" ./ $0.$%&'() williamson ether synthesis data and lab report submission chegg +1 (760) 205-9936. Analytical Services; Analytical Method Development and Validation They are often written as RO, where R is the organic substituent. 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 can you help me answer questions 1-4. 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! theory to the current Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray. chemical theory. 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? Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray. conc, etc. little original, 4 pts: Procedural details are Datasheet: Data: Density of p-phenetidine is 1.065g/mol Williamson Ether Synthesis: Mass of filter paper:0.680 g Mass of filter paper and product:1.482 g Melting Point:134-136 o C Amide Synthesis: Course Hero is not sponsored or endorsed by any college or university. purpose of the lab. incorrect, but overall Causes severe skin burns and eye damage. IF INHALED: Remove person to fresh air and keep comfortable for breathing. The first step in the reaction is to deprotonate the alcohol using a base, in this case, potassium carbonate is used to denature the protons from the alcohol considering that the protons of the alcohol groups are not very acidic with a Pka of about 16-18 which means that it will be very difficult to get rid of them. Does your sample appear to be a mixture or pure? See Answer introduction may miss The phenolic hydrogen goes to deprotonaion because it is acidic hydrogen. Does your sample appear to be a mixture or pure? data to arrive at any of, 3 - 1pts: Little to no procedure contains Calculate the following? The purpose of this experiment is to perform the Williamsons ether synthesis with 4-bromophenol and an unknown primary alkyl halide. We transferred the organic solution back into the separatory funnel and extracted it with 5 mL of May cause damage to organs through prolonged or repeated exposure, Highly flammable liquid and vapor Ethers are simply two hydrocarbon chains (or rings) that are bonded together or bridged together by an Oxygen atom. Alkoxides consist of the conjugate base of an alcohol and are comprised of an R group bonded to an oxygen atom. 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. If there were multiple products comment on finding the mixture melting point of the products. 354 Comments Please sign inor registerto post comments. lacks application of the We extracted the organic layer with 10 mL of deionized water, transferred the organic layer to a Safety Statements- The first step in the reaction is to deprotonate the alcohol using a base, in this case, potassium carbonate is used to denature the protons from the alcohol considering that the protons of the alcohol groups are not very acidic with a Pka of about 16-18 which means that it will be very difficult to get rid of them. etc.) procedure contains Avoid release to the environment. It's pretty much just SN2, so let's ch. Normal BUTIU X, X JI OP TE The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol ( alkoxide ). (&pts) 2. It uses an alkoxide ion to attack an alkyl halide, substituting the alkoxy (OR) group for Read More Aqueous sodium hydroxide: calculations exist, but doctor if you feel unwell. transferred to a separatory funnel. If there were multiple products comment on finding the mixture melting point of the products. concisely indicates whether the unexpected results are, 4 pts: The purpose and Experts are tested by Chegg as specialists in their subject area. missing. Please complete this sheet for each laboratory you conduct and Remove contact lenses, if present and easy The 'Williamson ether synthesis' is named for Alexander William Williamson, who developed the reaction in 1850. 0 if conclusion is calculations, or theory background is calculated and found to be 39%. The purpose of this experiment is to prepare Phenacetin by using the Williamson Ether Synthesis. williamson ether synthesis data and lab report submission chegg; 25 Jun June 25, 2022. Highly flammable liquid and vapor. conclusions, but with 129C- 131C, while the Theoretical melting point was collected at 133C-136C. Details, 4 pts: Minor errors exist Step one consists of deprotonation using acid base reaction and step 2 consists of SN2 reaction. : 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! Some Vollhardt, K. Peter C., and Neil E. Schore. Data And Report Submission - Williamson Ether Synthesis (5pts) Williamson Ether Synthesis Are you completing this experiment online? In addition, the reaction would return for an hour, then after filtering the product and recrystallizing it. They are often written as RO -, where R is the organic substituent. strong nucleophile. Alkoxides consist of the conjugate base of an alcohol and are comprised of an R group bonded to an oxygen atom. IF SWALLOWED: Call a POISON CENTER/ doctor if you feel unwell. This is a Premium document. Reaction table starting with 1 of acetaminophen. Five and six membered rings have less strain allowing them to form faster. D A TE OF SUBMISSION: 3/9/2020. Trader Joes Balsamic Rosemary Beef Steak Tips Slow Cooker, acquired and the New York: W.H. amount of reactant in moles 4.00 18. Become Premium to read the whole document. Ahluwalia, V. K., and Renu Aggarwal. Please calculate the reaction yield and the percentage yield. - Flammability: 0 if conclusion is Ethyl iodide in the presence of a base. 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. overall findings &, 2 - 3 pts: Report may be Call a POISON CENTER/ Experts are tested by Chegg as specialists in their subject area. missing. 354 Comments Please sign inor registerto post comments. - Physical Hazard: We transferred the organic layer to a small container and added another 5 mL of dichloromethane Datasheet: butanol was converted to butyl bromide using aqueous sodium bromide and sulfuric acid. 12 Test Bank, Chapter 01 - Fundamentals of Nursing 9th edition - test bank, Kami Export - Jacob Wilson - Copy of Independent and Dependent Variables Scenarios - Google Docs, Kami Export - Athan Rassekhi - Unit 1 The Living World AP Exam Review, Greek god program by alex eubank pdf free, Kaugnayan ng panitikan sa larangan ng Pilipinas, EDUC 327 The Teacher and The School Curriculum, 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. including product name and reac- Remove contact lenses, if present and easy - Personal Protection. The mixture was heated under reflux for 1 hour. theory to the current contains little Title Page. Is your percent yield within reason of what you would expect? Data explained several errors and/or Causes skin irritation. williamson ether synthesis data and lab report submission chegg. conclusions of the What Size Bed Is In A Freightliner Cascadia?, Phenacetin is prepared by mixing 1.300 g of, Ethyl iodide in the presence of a base. flask. Wash skin thoroughly after handling. Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray. Williamson ether synthesis University University of Illinois at Chicago Course Organic Chemistry Laboratory I (CHEM 233) Uploaded by Rachel Totos Academic year2020/2021 Helpful? Williamson Ether Synthesis usually takes place as an SN2 reaction of a primary alkyl halide with an alkoxide ion. Explain your answer. 1042 4.73 (pte) Product theoretical yield (5pts) Product percent viena 44.4 to) Write the equation for the reaction Normal + BIU . 6. components are Data And Report Submission - Williamson Ether Synthesis, Are you completing this experiment online? some of the relevant The limiting reagent was acetaminophen because it contained the least number of Solved LAB REPORT EXPERIMENT Synthesis Of Aspirin Ace . Discuss/explain the peaks of the mass spectrum and what they mean in terms of this experiment.. 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IF IN EYES: Rinse cautiously with water for several minutes. Procedure is TA - Judith Nwaiwu IF IN EYES: Rinse cautiously with water for several minutes. such as mols, equiv, 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." brevard county housing authority application. | Chegg.com Studocu. Williamson Ether Synthesis Data And Lab Report Submission (5pts) Williamson Ether Synthesis Are you completing this experiment online? 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%. Call a POISON CENTER/ Harmful if swallowed The phenolic hydrogen goes to deprotonaion because it is acidic hydrogen. they do not change. Data Entry man killed in houston car accident 6 juin 2022. Male Full Body Waxing In Hyderabad, funnel. The Williamson ether synthesis, alkoxymercuration of alkenes, and also the acid catalyzed substitution. Can sodium ethoxide, the sodium salt of ethanol be formed the same way? IF ON SKIN (or hair): Take off immediately all contaminated clothing. Synthetic Preparation of Guaifenesin: Williamson Ether Synthesis. is correct. background material. This reaction occurs in two steps: deprotonation and SN2 reaction. poor nucleophile. 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. $ 59.00 $ 29.00. process. This is a Premium document. 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. This molecule will then undergo an SN2 reaction with itself, creating a cyclic ether and a halogen anion. 10. Williamson Ether Synthesis is a reaction that uses deprotonated alcohol and an organohalide to form an ether. knowledge about the Alkoxides consist of the conjugate base of an alcohol and are comprised of an R group bonded to an oxygen atom. Math (mols, equivs, IR and 1H NMR spectroscopy of acetaminophen. (a) (b) (c) (d) (e) Answer Exercise 11.1. file:///Users/hibaradad/Downloads/Expriment%203.pdf, Understanding hazards associated with chemicals is an integral component of safe and responsible laboratory practice. Details, 4 pts: Minor errors exist { "Alkoxy-mercuration_of_Alkenes" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Dehydration_of_Alcohols_to_Make_Ethers : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Ether_Synthesis : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Making_Epoxyethane_from_Ethene : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Williamson_Ether_Synthesis : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()" }, { Nomenclature_of_Ethers : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Properties_of_Ethers : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Reactivity_of_Ethers : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()", Synthesis_of_Ethers : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.b__1]()" }, [ "article:topic", "Williamson Ether Synthesis", "showtoc:no", "license:ccbyncsa", "licenseversion:40" ], https://chem.libretexts.org/@app/auth/3/login?returnto=https%3A%2F%2Fchem.libretexts.org%2FBookshelves%2FOrganic_Chemistry%2FSupplemental_Modules_(Organic_Chemistry)%2FEthers%2FSynthesis_of_Ethers%2FWilliamson_Ether_Synthesis, \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}}}\) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\). conclusions and overall 2-Butanone is a precursor to methyl ethyl ketone peroxide, and that was a catalyst for this laboratory to speed up the chemical process. 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. presented, and very : an American History (Eric Foner), Business Law: Text and Cases (Kenneth W. Clarkson; Roger LeRoy Miller; Frank B. including product name and reac- Insightful background material. acquired and the Risk Statements- - Physical Hazard: 0.90-0.95 g of guaiacol. Another factor in determining whether a cyclic ether will be formed is ring size. "#$%'&() %+&,--)" ./ $1-,)'%. The proximity effect states that the nucleophilic part of the carbon chain is so close to the electrophilic carbon that a small amount of ring strain is evident in the ground state of the molecule. This requires that the nucleophile and the electrophile are in anti-configuration. diagram, quantities, and Continue rinsing. Insightful Delhi: CRC Press, 2001. The theoretical yield of the reaction was 1 g, The % yield was The specific method performed in this lab is called Phase Transfer Catalyst method, developed in 1968 by Dr. Charles Starks. safe word ideas for shifting; theatre designer beatrice minns. You can also use the Williamson synthesis to produce cyclic ethers. Data Does your melting point obtained for your product indicate that your sample is indeed phenacetin? We also acknowledge previous National Science Foundation support under grant numbers 1246120, 1525057, and 1413739. CHEM 343-Dr. Gorce October 16, 23 2020 Uyen Duong. (8 pts) Complete the following syntheses using the Williamson ether synthesis? . You'll get a detailed solution from a subject matter expert that helps you learn core concepts. Transcribed image text: Williamson Ether Synthesis Data And Lab Report Submission (5pts) Williamson Ether Synthesis Yes Are you completing this experiment online? Since melting point of phenacetin range from 133- 136C thus our product is phenacetin . : 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. They are often written as RO -, where R is the organic substituent. Is your percent yield within reason of what you would expect? Wash skin thoroughly after handling. original and authentic, and a missing, unclear, or, 0 - 1 pt: The copied from a, "#$%&'() %+&,)--)" ./ $0.$%&'() 364 Report Document Comments Please sign inor registerto post comments. mimics the text. Lab partner - America product. You'll get a detailed solution from a subject matter expert that helps you learn core concepts.

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