sulfate than cyclohexanol‚ excess anhydrous sodium sulfate may lead to the absorption of cyclohexane and thus loss of product. Anhydrous sodium sulfate absorbs water due to its polarity and therefore may also absorb cyclohexanol because of its polar O-H bond. If too much anhydrous sodium sulfate was added to the solution‚ part of the product would be absorbed too and thus a yield of less than 100% would be produced. 2. Lithium aluminum hydride would also reduce cyclohexanone to cyclohexanol. List three
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Exercise DP.1: Estimating Pure Component Properties in Hysys Workshop Report Requirements: 1. Create a graph of the vapor pressure in psia of cyclohexanol‚ cyclohexanol and high boiler as a function of temperature from 50 to 450 F. Print and submit these graphs. 2. Compare the pure component critical properties ( Critical Temperature‚ Critical Pressure) given in the design problem statement against the values used by Hysys. ( To view properties of a component‚ View the Basis Environment
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and cyclohexanol‚ the alcohol or A component)‚ or of pure cyclohexanol‚ and its subsequent oxidation in solution to adipic acid using an excess of strong nitric acid. This report deals with KA oil/cyclohexanol production by various routes‚ followed by the common step of nitric acid oxidation. KA oil production from cyclohexane by the cobalt catalyst and boric acid air oxidation routes is reviewed. Production of KA oil from phenol is also covered‚ as is the Asahi process for cyclohexanol production
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Experiment 8: Synthesis of Adipic Acid Performed November 8th & 10th By Jennifer Seitz Organic Chemistry 344 Section 803 Fall 2011 Objective: The purpose of this experiment was to synthesize adipic acid from cyclohexanol via an oxidation reaction that was catalyzed by sulfuric acid. Purity of the product was assessed by measuring the melting point. Physical Properties/Structures: Name | Formula | Molecular Weight (g/mol) | Boiling Point (0C) | Melting Point(0C) | Density(g/mL)
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In the first experiment‚ cyclohexanol was oxidized to form cyclohexanone. This was accomplished by pouring 2.0 ml of cyclohexanol and 1.0 ml of acetic acid into a 250 ml Erlenmeyer flask. Under a fume hood‚ slowly add 30 ml of bleach‚ and oxidizing agent‚ to the mixture and stir for 20 minutes. Acetic acid will react with bleach to make it a better oxidizing agent and form hopochlorous acid. Hypochlorous acid will then oxidize cyclohexanol. The mixture turned cloudy during the process but clear up
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YOUR NAME: Erin Alston‚ Kennedy Stuart‚ Amber Lamb and Stephonya Williams EXPERIMENT TITLE: Oxidation: Cyclohexanone from Cyclohexanol by Hypochlorite Oxidation and Adipic Acid from Cyclohexanone DATE: 4/18/2014 INTRODUCTION: In experiment 4‚ alcohol is oxidized to a ketone with household bleach. The product is then isolated by steam distillation and is extracted into the distillate with ether. After the removal of ether‚ it leaves the product cyclohexanone. In experiment 6‚ cyclohexanone is
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3168‚ Australia Received 13 October 1998; received in revised form 22 December 1998; accepted 23 December 1998 Abstract The oxidation products of cyclohexene "nd several applications as intermediates for the manufacture of useful chemicals like cyclohexanol‚ cyclohexenol/cyclohexenone‚ cyclohexadiene‚ etc. The uncatalysed oxidation of cyclohexene with molecular oxygen was studied in a batch reactor. The products‚ cyclohexene hydroperoxide‚ cyclohexenol‚ cyclohexenone and cyclohexene oxide were realised
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Procedure: The addition of 4.0 mL cyclohexanol‚ 1.0 mL of 85% phosphoric acid‚ and one boiling chip‚ were all added to a 10 mL round bottom flask that would be attached to the end of an assembled simple distillation set up. A sand bath was placed atop a hot plate‚ and the simple distillation mechanism was lowered into the sand bath with the bottom most piece (the 10 mL round bottom flask) submerged about half way. The distillation process was completed after a sufficient amount of liquid distillate
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OXIDATION OF CYCLOHEXANOL TO CYCLOHEXANONE The oxidation of cyclohexanol to cyclohexanone involves the removal of hydrogen from the OH group. After separation and purification‚ an Infrared Spectrum will be run to determine the composition of the recovered material. Infrared Spectroscopy is a very powerful technique used in the determination of molecular structure and the identification of unknown organic materials. The infrared spectrum yields direct
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E. 4‚2‚1‚3 1‚4‚2‚3 1‚3‚4‚2 4‚1‚2‚3 2‚1‚4‚3 OH OH HO OH 1 2 3 4 L. What is the IUPAC name of the following alcohol? A. S-2-ethyl-5‚5-dimethyl-R-cyclohexanol B. R-2-ethyl-5‚5-dimethyl-R-cyclohexanol C. S-2-ethyl-5‚5-dimethyl-S-cyclohexanol D. S-6-ethyl-3‚3-dimethyl-cyclohexane E. S-3-ethyl-R-6-S-6-dimethyl-cyclohexanol HO M. Predict the most likely mechanism(s) for the reaction of cis-3-methyl-chloro-cyclohexane with sodium methoxide (in methanol as the solvent) – circle one
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