Title: Diffusion in Gases I Aim: To observe the diffusion of bromine Apparatus and Materials: Glass tube‚ bromine‚ fume chamber Diagram: Procedure: -Liquid bromine was placed in a jar and covered Observations: When first placed in the jar the original color of bromine was red-brown. As it began to diffuse its color changed from dark brown to a lighter brown until it becomes a yellow-like orange color. As it was diffusing liquid bromine changes its state to gaseous. With an odour given off smelling
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product‚ why selective?‚ is this molecule chiral?) Bromine was added to Estilbene to form an anti product. This happened because no true carbocation was formed in reaction. Instead‚ there was an intermediate where one of the bromine atoms was partially bonded to both carbon atoms of the double bond. This prevented bond rotation around the carbon-carbon bond. The steric hindrance prevented the bromine from being added to the same side as the first bromine atom. Thus‚ the process of bromination was stereoselective
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Description The students titrate different oils and fats mixed with Volasil against bromine water. Apparatus and equipment (per group) w White tile w Conical flask w Dropper pipette. (Use the type of teat pipette usually fitted to Universal Indicator bottles‚ that do not allow squirting – eg Griffin.) w Burette (filled with bromine water) w Boss w Clamp w Stand. Chemicals (per group) –3 w Bromine water (Harmful and irritant) 0.02 mol dm (This concentration does not have to be accurate
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Acetylene gas was used for the selective reactivity of hydrocarbons to functional group tests; Bayer’s test‚ Bromine test light‚ Bromine test dark‚ and Tollen’s test. In Bayer’s test‚ only Acetylene‚ Eugenol and Unknown hydrocarbon 2 reacted positively and the rest retain the purplish color of KMnO4. On the other hand‚ the five compounds in Bromine test with light reacted positively. In Bromine test dark‚ Hexane and Unknown hydrocarbon 1 did not react because light (UV) is absent. Lastly‚ in Tollen’s
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required reagent of concentrated sulfuric acid as one of the catalyst and water which allow the mixing known as washing the cyclohexene with water. The formation of product cyclohexene which is reweight and adding of bromine the last reagent for confirming that is alkene known as bromine test which leads to colour changes. Yet this experiment reflects some important discussion and conclusion for the formation of cyclohexene. INTRODUCTION One of the common ways of preparing an alkene is through
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found to determine syn or anti addition of bromines. The melting point was 199-203°C and the NMR J values angle is at 167 which both prove the erythro-2‚3-dibromo-3-phenylpropanoic. Determination of the Stereochemistry of 2‚3-dibromo-3-phenylpropanoic acid. Introduction The purpose of this experiment was to determine the mechanism of the reaction of trans-cinnamic acid with the addition of bromines to 2‚3-dibromo-3-phenylpropanoic acid. An addition of bromine was added to trans-cinnamic acid and it
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contain c-c single bonds‚ are saturated‚ and are the least reactive. Alkenes are c=c double bonds‚ more reactive than alkanes‚ and unsaturated. In the next part of the experiment we added bromine to alkenes. This caused an electrophilic halogenation reaction. If the bromine reacted with the alkene the bromine would discolor from orange and turn clear. Experiment Part A) Solubility of Alkanes: 1 mL of nine solvents (water‚ methanol‚ n-butanol‚ ethylene‚ glycol‚ acetone‚ hexane‚ toluene‚ ethyl
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different hydrogen atoms when reacted with bromine under free-radical substitution. The time it took for the bromine color to disappear was used to determine the order of reactivity of the different hydrocarbons. Data and Results The data of the 10 hydrocarbon tubes and the 2 control tubes with bromine and dichloromethane in the two different conditions is listed below in Table 1. As a result‚ the hydrocarbon tubes in light reacted and lost the bromine color quicker than the tubes not in light
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- College of Science‚ University of Santo Tomas‚ Manila ABSTRACT The unknown hydrocarbon sample was differentiated and characterized by the use of three tests. The outcomes of these tests are as follows: Nitration test (negative)‚ Bromine test (positive) and Basic Oxidation test (positive). From these results the unknown sample can be classified as non-aromatic and unsaturated. INTRODUCTION Hydrocarbons are organic compounds that consist of only C and H atoms. They include the
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Lewis base. It can therefore be saturated by the addition of a halogen to the double bond. Both of the reactants are non-polar but there is an induced polarity during the reaction due to the electron-rich site at the double bond‚ which results in bromine acting as an electrophile. In this reaction‚ the cinnamic acid reacts as an alkene. Alkenes are unsaturated hydrocarbons with a carbon-carbon double bond. In a double bond‚ a pair of electrons lies between the carbon atoms in a σ bond and the other
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