color‚ and odor were noted through simple observation. Miscibility of the test compounds were noted through color change or a warming effect. Flammability was tested by igniting 3-5 drops of the sample in a small evaporating dish. Baeyer’s test and Bromine test were used for tests for active unsaturation. Aromaticity of the compound was determined through nitration. Oxidation was tested by introducing 8 drops of 2% KMnO4 solution and 3 drops of 10% NaOH solution to 4 drops of the sample organic compound
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bromination with hydrogen peroxide and hydrobromic acid‚ and debromination with zinc. The yields of parts A‚ B‚ and C are as follows: 68.6 %‚ 54.6 %‚ and 55.9 %. Introduction In the chemical process of bromination‚ an alkene is halogenated with bromine. Solvents that are typically used include methylene chloride and carbon tetrachloride along with iodine‚ the traditional reagent. However‚ because of the carcinogenic properties of the solvents and the corrosiveness of iodine‚ other alternatives are
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The purpose of the lab “All in the Family” was to compare the reactivity of the halogens Chlorine‚ Bromine‚ and iodine by observing the reactions between their elemental forms and their ionic forms. To accomplish this experiment‚ we first added a squirt of pet ether to two test tubes. Then‚ we added the same amount of Cl2 to both of the tubes‚ shook the mixtures‚ and recorded the color that resided in each mixture as the initial color. After‚ a squirt of NaBr was added to one test tube‚ and a squirt
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is finally tested to determine whether or not it has been dehydrated. The three tests used were infrared spectroscopy‚ Bromine chemical test and Bayer’s chemical test. The infrared spectroscopy showed a large narrow peak at 3062.12(cm-1) and 3020.71(cm-1) which indicates that there is a double bond present. To assure the results were correct the chemical tests were done. The Bromine test was found to be positive for cyclohexene. The OH group was removed from the cyclohexanol and replaced with a double
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BACHELOR OF SCIENCE (HONS) BIOTECHNOLOGY YEAR 1 SEMESTER 1‚ 2 & 3 UDBB 1164 FUNDAMENTAL ORGANIC CHEMISTRY 0 EXPERIMENT 1 PROPERTIES OF HYDROCARBONS Introduction Hydrocarbons are compounds which contain only carbon and hydrogen‚ can be classified into several types‚ depending on their structure. Aliphatic hydrocarbons are divided into three classes: alkanes (e.g. methane‚ ethane and propane) have only single bonds‚ and are said to be saturated; alkenes (e.g. ethene and propene)
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following substance freezes at 39oC? a) Copper b) Mercury c) Steel d) Bromine 5. Which of the following substance boils at 357oC? a) Bromine b) Steel c) Copper d) Mercury 6. Which of the following substance has all the properties that should be present in thermometric materials? a) Mercury b) Bromine c) Steel d) Copper 7. Which thermometers are widely used in laboratories? a) Mercury-in-glass thermometers b) Bromine-in-glass thermometers c) Steel-in-glass thermometers d) Copper-in-glass
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1 Ethene may be converted into poly(ethene). What type of reaction is this? (A) Condensation (B) Hydrolysis (C) Oxidation/reduction (D) Polymerisation 2001:1 1 2 You have carried out a first-hand investigation to compare the reactivity of an alkene with its corresponding alkane. (a) State the name of the alkene. 2002:16(a) 1 (b) Outline a procedure to compare the reactivity of this alkene with its corresponding alkane. 2002:16(b) 2 (c) Describe the
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University of Maryland‚ College Park Department of Chemistry and Biochemistry CHEM 231: Organic Chemistry I‚ Fall 2014 The Highlights Bonnie Dixon TA: Courney Love Office: CHM 2130 email: bdixon1@umd.edu email: clove@umd.edu When/Where: Lecture MWF 9 a.m. – 10 a.m. in CHM 1407 Discussion T/H at 12:30 pm‚ 2 pm‚ and 3:30 pm in the CHM 1228 Course Materials: Organic
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Organometallic preparation and addition to carbonyls‚ Wittig reagent preparation and Wittig rxn‚ Wolff‚ H-based nucleophile carbonyl reduction‚ imine formation‚ reductive amination (rxn only)‚ ketal/acetal formation‚ dithiane chemistry (rxn only)‚ alpha-bromination of ketones‚ -COOH properties (the trends on HW4)‚ Fischer‚ acidic/basic hydrolysis of esters/amides/nitriles‚ CH2N2‚ acid chloride formation (rxn only)‚ acid chloride rxns with esters and amides. 2 Rxn of carboxyllic acid derivatives
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structures; • describe the reactions involved in the preparation of haloalkanes and haloarenes and understand various reactions that they undergo; • correlate the structures of haloalkanes and haloarenes with various types of reactions; • use stereochemistry as a tool for understanding the reaction mechanism; • appreciate the applications of organo-metallic compounds; • highlight the environmental effects of polyhalogen compounds. Haloalkanes and Haloarenes Haloarenes Halogenated compounds persist
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