ASynthesis of an alkyl halide Jade A. Chuahiong and Marika Bianca F. Morioka Institute of Chemistry‚ University of the Philippines‚ Diliman‚ Quezon City 1101 Philippines Date Performed: April 25‚ 2013; Date Submitted: April 30‚ 2013 Alkyl halides could be synthesized through several processes and using different compounds as reactants. One of the simplest method used is the addition of a hydrogen halide to an alcohol. In this research‚ tert-butyl alcohol was reacted with cold concentrated
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SYNTHESIS OF AN ALKYL HALIDE S.M. BLANCAFLOR1 1INSTITUTE OF BIOLOGY‚ COLLEGE OF SCIENCE UNIVERSITY OF THE PHILIPPINES‚ DILIMAN‚ QUEZON CITY 1101‚ PHILIPPINES DATE SUBMITTED: 3 JANUARY 2012 DATE PERFORMED: 8 DECEMBER 2011 ------------------------------------------------- ABSTRACT Alkyl halides are molecules which have a carbon atom attached to a halogen atom (e.g.‚ chlorine‚ iodine‚ or bromine.) Alkyl halides are very important since they are used in many of the products used today
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Experiment 6: Synthesis of an Alkyl Halide Maria Alexandria Buraga Ammuyutan Institute of Chemistry‚ University of the Philippines‚ Diliman‚ Quezon City 1101 Philippines ------------------------------------------------- Department of Food and Science Nutrition‚ College of Home Economics‚ Univeristy of the Philippines‚ Diliman‚ Quezon City 1101 Philippines ------------------------------------------------- ABSTRACT ------------------------------------------------- Alcohols react with hydrogen
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Substitution | Synthesis of n-Butyl Bromide and t-Pentyl Chloride | | Jessica | [Pick the date] | Abstract The synthesis of the alkyl halide n-Butyl Bromide from alcohol is the foundation for the experiment. During the isolation of the n-butyl bromide‚ the crude product is washed with sulfuric acid‚ water‚ and sodium bicarbonate to remove any remaining acid or n-butyl alcohol. The primary alkyl halide halide n-butyl bromide is prepared by allowing n-butyl alcohol to react with sodium bromide and sulfuric
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Relative Reactivity of Alkyl Halides Introduction Nucleophilic substitution of alkyl halides can proceed by two different mechanisms – the SN2 and the SN1. The purpose of the experiment was to identify the effects that the alkyl group and the halide-leaving group have on the rates of SN1 reactions‚ and the effect that the solvent has on the rates of SN1 and SN2 reactions. The SN1 mechanism is a two-step nucleophilic substitution‚ or unimolecular displacement. In the first step of the mechanism
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Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction Unknown Letter: B 23 April 2013 Academic Integrity Statement: “Experimental data may be collected with other students in organic chemistry labs. However I understand that sharing information required for a lab report (including but not limited to word processing or spreadsheet files‚ calculations‚ graphs‚ conclusions and additional problems at the end of the lab report) with other students is a violation of the University
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Lab 5 n-Butyl Bromide Preparation Introduction: The purpose of this lab is to properly extract and distill n-butyl bromide It is ideal to perform this technique with accuracy‚ which can be measured by the percent yield. Chemicals: n-Butyl Bromide- clear‚ yellow liquid that is slightly soluble in water. Molar weight of 137.02g and has zero reactivity. Sodium Bromide- white‚ crystals‚ granules. Soluble in water with no reactivity. Molar weight of 102.89g. Sulfuric Acid- colorless liquid
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This paper is submitted by Anupam Basu LAB (Linear Alkyl Benzene):- For more than 30 years‚ UOP has been a leading innovator in the production of LAB. During that time‚ we’ve developed the state-of-the-art technology you’ll need to ensure that your new or revamped LAB complex operates most efficiently and produces the highest quality product.LAB is the primary raw material used in the production of linear alkyl benzene sulfonate (LAS). LAB is produced from benzene and long chain normal paraffins
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Conversion of Alcohols to Alkyl Halides Ankita Patel August 6‚ 2013 Introduction This lab consisted of the conversion of alcohols into alkyl halides through common substitution methods. These methods include SN1 and SN2 mechanism‚ both of which can occur for this type of reaction. For both reactions‚ the first step of protonation will be to add hydrogen to the –OH group and then the rest of the reaction will proceed according to the type of mechanism. SN1 reactions form a cation intermediate
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n-butyl bromide or n-bromobutane‚ which is derived from an alcohol and an acid. In this case‚ n-butyl alcohol and sulfuric acid were the reagents. There were two methods of distillation that was involved in this experiment. The first was by reflux distillation‚ which is used to speed up a chemical reaction without having the reactants/ products evaporate or explode. Data Table 1 indicates the amount of each reagents that was prepared for the reflux apparatus. However‚ the reagents‚ sodium bromide‚ water
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