skeleton: CH3 H3C CH3 2. The molecule trans-cyclooctene is known to exist. (It is chiral‚ by the way). Why is the analagous molecule trans-cyclohexene unstable? Far too strained to have a trans-alkene in a six-membered ring. H H H = H H H trans-cyclooctene (planar representation) trans-cyclooctene (perspective representation) trans-cyclohexene???? 3. Draw each of the following bicyclic alkenes in a good "perspective" representation. Only one of these three compounds actually exists
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Identification Using Infrared Spectroscopy Aim: To identify the functional groups in organic compounds using infrared spectra. APPARATUS AND REAGENTS: Nicolet 380FTIR‚ HATR Accessory (liquid crystal plates) Reagents ( Methanol‚ Benzene and Cyclohexane‚ Cyclohexene) THEORY: An important tool of the organic chemist is Infrared Spectroscopy‚ or "IR". IR spectra are acquired on a special instrument‚ called an IR spectrometer. IR is used to gather information about compound ’s structure‚ assess its purity‚ and
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Maleic anhydride underwent the Dials-Alder reaction with distilled cyclopentadiene as the dienophile. The reaction was a cycloaddition which produced cis-Norbornene-5‚6-endo-dicarboxylic Anhydride surface. (1) Product one had a mass of 9.351 grams and product two had a mass of 9.572 grams. The theoretical yield was found to be 10.047 grams‚ which makes the percent yield to be 93.07%. Melting Points were found to confirm the purity of the product. Product one had a melting point of 163.7-164
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Analysis of Hydrocarbons Jennifer Alambra‚ Ma. Nancy Anulat‚ Alfonso Apepe*‚ Jacqueline Arsenal 3Bio4 Department of Biological Sciences - 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
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LETTER OF TRANSMITTAL 2nd May 2011 Md. Firoz-Al-Mamun Assistant Professor Faculty Of Business ASA University Bangladesh Subject: Submission of term paper. Dear Sir‚ With due respect it is our pleasure to present the term paper entitled ‘‘Marketing Plan”. While preparing the statement we have tried our best to create a perfect Marketing Plan and tried to show all sort of planning and project works that is required to make the plan perfect. We have collected all the up-dated information
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Diels-Alder Reaction Heather Jost Lab Partner: Jasmina Salcinovic CHEM2642L Luise Strange de Soria Georgia Perimeter College September 29‚ 2004 Diels-Alder Reaction Resources: Mayo‚ Pike‚ Trumper‚ Strange de Soria. Microscale Organic Laboratory. New York: John Wiley and Sons‚ 2002. Strange de Soria‚ Luise. “Student Survival Guide”. http://www.gpc.edu/~lstrange/2642lab/survivalguide/grignard2.pdf. 2004. Purpose: The purpose of these experiments
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C2H4 (g) + H2 (g) [pic]C2H6 (g) – Hydrohalogenation (more specifically‚ Hydrofluorination) of ethylene: ▪ ethylene + hydrogen fluoride [pic] fluoroethane ▪ C2H4 (g) + HFl (g) [pic]C2H5Fl (g) – Reaction of cyclohexene with bromine water: ▪ cyclohexene + bromine water[pic] 2-bromo-1-cyclohexane ▪ C6H10 (l) + Br2 (aq) [pic] C6H10Br2 (aq) – Reaction of cyclohexane with bromine water (subsitution reaction‚ only under sunlight‚ that is UV light): ▪ C6H12 (l) + Br2(aq)
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alcohol with concentrated hydrochloric acid. Q6. Explain why the solution became milky white in appearance after adding 11 M HCl(aq) to the tertiary butyl alcohol. Q7. A student is given two alcohols with which to perform Lucas Test. These are cyclohexanol and 2-methyl-2-propanol. The bottles containing each alcohol are labelled‚ but the propettes used are not. The student accidentally muddles the propettes. When drops of each alcohol are mixed with Lucas. Reagent and kept at 27 °C‚ both solutions
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DETAILED LESSON PLAN IN ADVANCED CHEMISTRY IV- Euler LEARNING OBJECTIVES At the end of the lesson‚ students are expected to: Write the IUPAC name of certain alcohol compounds; SUBJECT MATTER Topic: Nomenclature of Carboxylic Acid References: General‚ Organic and Biochemistry by Denniston‚ Topping and Caret. Page 283-289. Fundamentals of General‚ Organic and Biochemistry by John R. Holum. Page 418-425. Materials: Ball and stick model of compounds Overhead projector Textbooks Pictures of certain
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DEHYDRATION OF 4-METHYLCYCLOHEXANOL PURPOSE Perform an acid-catalyzed dehydration of 4-methylcyclohexanol to produce 4-methycyclohexene. TECHNIQUES • Dehydration of an alcohol • Preparation of an alkene • Distillation • Unsaturation tests THEORY An acid-catalyzed dehydration is a common way to synthesize an alkene from an alcohol. Use of a strong acid like sulfuric or phosphoric acid serves to protonate the alcohol "OH" group‚ forming an H2O molecule that is a much better leaving group
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