"Cyclohexene cyclohexanol" Essays and Research Papers

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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 cyclohexanolcyclohexanol 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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    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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    2423L8

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    and unsaturated hydrocarbons using properties and reactions. b) Study substitution and addition reactions. Equipments test tube rack (1) test tube holder (2) 100 mL beaker medium test tube (6) Materials cyclohexene toluene n-hexane conc. H2SO4 Br2/CCl4 or Br2/CH2Cl2 0.50 % KMnO4 10% NaOH 10% Na2CO3 unknowns hydrocarbons Discussion Hydrocarbons‚ compounds which contain only carbon and hydrogen‚ can be classified into

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    properties of hydrocarbon

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    unknown samples. Results : Part A : Combustion Compounds Observations Hexane There was orange flame and burned mildly during the burning process. No soots and smoke were produced. C6H14 + 19/2 O2 6CO2 + 7H2O Cyclohexene Orange flame burned vigorously. A small amount of black soot and smoke were produced during the burning process. C6H10 + 17/2 O2 6CO2 + 5H2O Toluene Orange flame burned very vigorously. A large amount of black soot and smoke

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    Muhammed Sabah Comparing Reactivity Of Alkanes and Alkenes Aim: To compare the reactivity of an alkane and an alkene Hypothesis: The cyclohexene would react to the bromine water and turn colourless‚ whilst the cyclohexane won’t react. Risk Assessment: What’s the problem? | How do you fix? | How does it work? | Bromine water is corrosive to the skin | Wear gloves | Stops the Bromine water from reaching skin | Cyclohexane/ene is highly flammable | Keep away from naked flames. | No naked

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    Reactions of Hydrocarbons

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    Properties and Reactions of Hydrocarbons Abstract Introduction Hydrocarbons are organic materials that contain only carbon and hydrogen atoms‚ these molecules can be saturated or unsaturated and acyclic‚ cyclic‚ or aromatic. In this experiment we used a variety of methods to examine the physical and chemical properties of hydrocarbons. The first experiment we tested a variety of solvents to see if they dissolved our alkane (Decalin). One would expect that non-polar solvents will dissolve

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    Synthesis of Adipic Acid

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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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    Evan Evaristo Department of Occupational Therapy‚ College of Rehabilitation Sciences University of Santo Tomas‚ Espaňa Street‚ Manila 1008 Date Submitted: February 2‚ 2011 Abstract: Organic compounds hexane‚ heptane‚ cyclohexane‚ cyclohexene‚ benzene‚ and toluene were subjected to different physical and chemical tests todifferentiate their intrinsic physical properties and chemical properties in terms ofstructure and behaviour. Nitration test (test for the presence of aromatic ring)

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    Cyclohexanone Lab Report

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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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    Abstract The preparation of 7.7-dichlorobicyclo [4.1.0]heptane which is also known as 7‚7-dichloronorcarane was done by reacting cyclohexene ‚ chloroform and a base( 50% aqueous sodium hydroxide) with benzyl triethylammonium chloride. The latter being a water soluble phase transfer catalyst (PTC).reaction was performed at room temperature and was distilled at atmospheric pressure. The mechanism of action of the above mentioned PTC is described in the text along with the mechanism for the addition

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