Introduction to Alkane Nomenclature A. Determining the Priority of Functional Groups. What’s in a name? 3-ethyl-5-(1-methylpropyl)-4‚4-dimethylnonane Too big a subject to cover on one sheet! This paper will focus on alkanes. Determining functional group priority will be the subject of a subsequent sheet. suffix http://masterorganicchemistry.com D. Applying the Lowest Locator Rule F. Dealing With Branched Substituents (the IUPAC Way) Number the chain from one end so as
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through a Williamson Ether Synthesis reaction with an SN2 mechanism. Introduction In this two-week experiment‚ guaifenesin‚ an expectorant found in over-the-counter cough syrups and tablets‚ was prepared through the Williamson Ether Synthesis model. The model involved an SN2 mechanism between the sodium phenoxide salt derived from guaiacol (2-methoxyphenol) and 3-chloro-1‚2-propanediol (Wildman‚ 2003). With the Williamson Ether Synthesis specializing in producing ethers‚ it was ideal for this
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Market and Nonmarket Environments Market environment includes those interactions (which involve voluntary economic transactions and the exchange of property) between firms‚ suppliers and customers that are governed by Markets and Contracts. Nonmarket environment is composed of the social‚ political and legal arrangements that structure interactions (between the firm and individuals‚ interest groups‚ govt. entities‚ and the public which are intermediated not by markets but by public and private
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Chemistry 2283g Experiment 1 – Alkyl Halides EXPERIMENT 1: Preparation and Reactivity of Alkyl Halides Relevant Sections in the text (Wade‚ 7 ed.) • 6.7 (p. 228) Reactions of alkyl halides • 6.8 – 6.12 (p. 229 – 242) The SN2 reaction: generality‚ factors affecting SN2 reactions‚ substrate reactivity‚ mechanism • 6.13 – 6.14 (p. 243 – 249) The SN1 reaction: mechanism‚ stereochemistry General Concepts The most common of the variety of methods available for preparing alkyl halides is the replacement
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William son Eth er Synth esis Introduction In this reaction‚ an alcohol is deprotonated to form a good nucleophile‚ which then attacks the electrophile methyl iodide to form an ether. Tetrabutylammonium bromide‚ a phase transfer catalyst‚ is used to carry ions back and forth between the organic phase and the aqueous phase. OH O NaOH + NaI + H2O CH3I Before coming to lab‚ please review the following techniques: "Reluxing a reaction‚" "Extraction and washing‚" "Drying an Organic Solvent‚" "Evaporating
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Experiment 7: Diethyl n- Butylmalonate Lab Partner: Reference: Williamson K.L.‚ & Masters‚ K.M. (2011).”Diethyl n- Butylmalonate”. Macroscale and Microscale Organic Experiments ( 6th edition pp. 531-534) Belmont‚ CA: Brooks Cole. Purpose: In this experiment‚ potassium carbonate combined with a quaternary
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fourth edition ORGANIC CHEMISTRY Francis A. Carey University of Virginia Burr Ridge‚ IL Dubuque‚ IA Madison‚ WI New York San Francisco St. Louis Bangkok Bogotá Caracas Lisbon London Madrid Mexico City Milan New Delhi Seoul Singapore Sydney Taipei Toronto | v v Boston | e-Text Main Menu | Textbook Table of Contents | Study Guide Table of Contents McGraw-Hill Higher Education A Division of The McGraw-Hill Companies ORGANIC CHEMISTRY‚ FOURTH EDITION
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Synthesis of Phenols You can prepare phenols in large quantities by the pyrolysis of the sodium salt of benzene sulfonic acid‚ by the Dow process‚ and by the air oxidation of cumene. Each of these processes is described below. You can also prepare small amounts of phenol by the peroxide oxidation of phenylboronic acid and the hydrolysis of diazonium salts. Pyrolysis of sodium benzene sulfonate In this process‚ benzene sulfonic acid is reacted with aqueous sodium hydroxide. The resulting salt
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SYNTHETIC EXPLOITATION OF ENZYMES: BIOCATALYSIS IN ORGANIC SOLVENTS: FUNDAMENTALS ENZYMES IN ORGANIC SYNTHESIS 1. Enzymes catalyze a broad spectrum of reactions with high turnover numbers. Rate enhancements approach 1012 fold. 2. Enzymes may accept a wide range of substrates. 3. Enzymes are highly regio and stereoselective. 4. Enzyme reactions take place under mild conditions; this minimizes problems of isomerization and racemization. 5. Enzymatic processes are less hazardous and polluting
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Carly Bolyard Chem 2020 Experiment Performed: 9/17/2014-9/24/2014 Lab Partner: Erika Breeden Synthesis of 1‚4-Di-t-Buytl-2‚5-Dimethoxybenzene via Friedel-Crafts Alkylation Title: Synthesis of 1‚4-Di-t-buytl-2‚5-dimethoxybenzene via Friedel-Crafts Alkylation Introduction: Friedel-Crafts alkylation of benzene (and substituted benzenes) involves substituting a hydrogen atom on a benzene ring with an alkyl group. In the reaction a new alkyl group becomes bonded to a carbon atom of
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