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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that would be used later on in quantitative analysis of percent yield of cyclohexene. Lastly‚ a bromine test was carried out to quantitatively test the presence of cyclohexene product in the prepared sample. A total of 2-3 drops of 3% bromine in dichloromethane was added to a new test tube as well one drop of the prepared cyclohexene. Upon observing a color change from brown to clear‚ one can confirm the presence of cyclohexene in the obtained
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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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Formation of an Alkene by Alcohol Dehydration Lab Report Balanced Chemical Equation for the Main Reaction Mechanism The acid-catalyzed dehydration of secondary and tertiary alcohols involves non-isolable carbocation intermediaries. In the first step of the of the reaction mechanism below‚ a phosphoric acid catalyst adds a proton to the oxygen atom of the alcohol to form an oxonium ion. The OH is converted to a better leaving group as the positive charge on the oxygen weakens the carbon-oxygen
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Institute of Technology; 2 Professor‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology [pic] ABSTRACT The purpose of this experiment is to prepare cyclohexene form cyclohexanol‚ and know the properties of alkene. The first part of this experiment is preparation of cyclohexene. Simple distillation set-up is assembled. (See Figure 1). Exactly 6.0mL of cyclohexanol is weighed in a quick-fit one-necked pear shaped flask. 1.50mL of 85% H3PO4 is measured using the
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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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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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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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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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