Title: Preparation of Cyclohexene from Cyclohexanol Aim: To prepare an alkene‚ cyclohexene‚ by the dehydration of an alcohol‚ cyclohexanol‚ and better understand the processes that take place during this reaction. Introduction: One of the common ways of preparing an alkene is through the dehydration of an alcohol. In this experiment cyclohexanol is dehydrated to prepare cyclohexene while using sulfuric acid as a catalyst. A bromine test can be later done to ensure that the end product is
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I. Objectives * Be able to prepare cyclohexene from the dehydration of cyclohexanol * Understand the mechanisms of the dehydration reaction (acid-catalyzed dehydration). * Know how to use the necessary equipment for this reaction‚ such as the fractioning column. * Obtain positive results in unsaturation tests for the presence of carbon-carbon double bond (cyclohexene). II. Background Cyclohexanol‚ the reagent of this experiment‚ is used in the production of nylon
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Cyclohexene Synthesis by Dehydration Reaction of Cyclohexanol Gjulia Vokrri 02-15-2013 Abstract Alkenes can be produced by heating and dehydrating an alcohol in the presence of a strong acid. The purpose of this experiment was to synthesize cyclohexene by dehydration of cyclohexanol and to detect the presence of a double bond in the alkene. The dehydration reaction using distillation was
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Alkene Synthesis from Alcohol: Preparation of Cyclohexene From Cyclohexanol 5/29/14 Abstract: A 42.89% yield cyclohexene was successfully synthesized from 10.0 mL cyclohexanol by unimolecular elimination (E1) through the dehydration of cyclohexanol and confirmed via a bromine test and the IR spectra. Introduction: Alkenes are hydrocarbons that have carbon–carbon double bonds and are one of the many functional groups in organic molecules. Alkenes are sp2 hybridized
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Nate Rhodes The Synthesis of Alkenes: Dehydration of Cyclohexanol Organic Chemistry Lab 1 Tuesday 8:00 11/08/11 Paul Jackson Abstract: The goal of this experiment was to form cyclohexene from cyclohexanol through a dehydration reaction. Cyclohexene was successfully synthesized according to the bromine test performed and the IR spectra. There was a percent yield of cyclohexene of 76.1%. Introduction: Alkenes‚ hydrocarbons containing at least one carbon-carbon double bond‚ are important
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Dehydrating Cyclohexanol • Introduction The purpose of the lab experiment is to prepare cyclohexene from cyclohexanol through an acid-catalyzed dehydration. In order to produce the cyclohexene from cyclohexanol‚ an elimination reaction was performed. First by protonating the oxygen of the alcohol and creating an oxonium ion we replaced the poor leaving group (OH) into a better leaving group (OH2+). Second‚ dehydrating the cyclohexanol using phosphoric acid and sulfuric acid as acid catalysts
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Synthesis of Cyclohexanol Author: Ahmed Ayyash 06/06/13 Introduction: In this experiment‚ cyclohexanol was prepared from an initial cyclohexene. However‚ this occurred over a number of steps‚ these are out lined below. 1. Cyclohexene + aqueous acid cyclohexyl cation 2. cyclohexyl cation + hydrogen sulphate + water protonated cyclohexanol + cyclohexyl hydrogen sulphate 3. cyclohexyl hydrogen sulphate protonated cyclohexanol + HSO4 4. protonated cyclohexanol + HSO4 ⇄
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Dehydration of Cyclohexanol Introduction In this experiment cyclohexene‚ an alkene‚ was prepared by the dehydration of cyclohexanol‚ an alcohol‚ using phosphoric acid‚ an acid catalyst. The reaction is as follows: [pic] The dehydration of cyclohexanol was performed in a simple distillation apparatus. As cyclohexene formed‚ it was distilled out of the mixture. Background Dehydration is an elimination reaction of an alcohol that takes place in the presence of an acid catalyst
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Introduction: Cyclohexanol is mainly used in the production of caprolactam and adipic acid that is a raw material of nylon 6 (Zhang‚ et al‚ 2002). Cyclohexanol can be produce through several methods‚ which include the oxidation of cyclohexane‚ the hydration of cyclohexene‚ or the hydrogenation of phenol (Zhang‚ et al‚ 2002). Problem with oxidation of cyclohexene is poor selectivity‚ extremely large recycles and explosion hazards. (Suresh‚ Sridhar‚ Potter‚ 1988). The purpose of this experiment was
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Oxidation of Cyclohexanol Introduction: The oxidation of cyclohexanol involves using household bleach to oxidize this secondary alcohol and produce a ketone product‚ cyclohexanone. Oxidation-reduction (redox) reactions occur when the oxidation state of atoms change due to a transfer of electrons. Oxidation occurs when electrons are ‘lost’ to the formation of bonds and reduction occurs when electrons are ‘gained’ in the braking of bonds (Levine). Using this reaction and its product‚ a redox experiment
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