suggested the presence of an aromatic ring‚ alkene group and carbonyl group. CNMR showed the presence of an aromatic ring‚ carbonyl group and a methyl group. HNMR showed the presence of an aromatic ring‚ alkene group and carbonyl. Using the rule of 13 and the adjustment for oxygen‚ the predicted structure of the anise oil was C10H12O with 5 degrees of unsaturation. Since the aromatic ring is 4 degrees of unsaturation by itself‚ the last degree of unsaturation was most likely an alkene
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4th form Chemistry questionnaire 1. All of the following structures show the same molecule‚ except one. Which structure is different? H H H H A) H -- C -- C -- C --- C -- H B) CH3 CH2 CH2 CH3 H H H H H H -- C -- H CH3 C) H H D)
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bromination of (E)-1‚2-diphenylethene (trans-stilbene) by addition reaction in which bromine was added across the double bond to yield a vicinal dibromide. The next step was to perform a double elimination reaction by product gained to synthesize an alkyne‚ that is‚ 1‚2-diphenylacetylene. The two major techniques used in this lab were TLC analysis and UV-vis spectroscopy. TLC technique is non-destructive‚ that is‚ the molecules in the mixtures are separated physically without being chemically altered
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to test for the presence of alcohol. The color changed to brown‚ indicating the presence of the desired product. A drop of the product was also tested with IR spectroscopy. There were peaks at both 1600cm-1 and 3300cm-1 which are indicative of an alkene. 1600cm-1 correlates with the C=C stretch‚ while the 3300cm-1 signal correlates
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0 PANJAB UNIVERSITY CHANDIGARH- 160 014 (INDIA) (Estted. under the Panjab University Act VII of 1947-enacted by the Govt. of India) FACULTY OF SCIENCE SYLLABI FOR M.Sc. (TWO YEAR COURSE ) IN CHEMISTRY 1st & 2nd YEAR( Semester System) EXAMINATIONS 2013-2014 --:O:-- 1 OUTLINES OF TESTS‚ SYLLABI AND COURSES OF READING FOR M.Sc. FIRST YEAR (SEMESTER-I) EXAMINATION OF 2013 OBJECTIVE OF THE COURSE To teach the fundamental concepts of Chemistry and their applications. The syllabus pertaining
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Experiment 11: Synthesis of Dibenzalacetone by the Aldol condensation Introduction: The Aldol condensation reaction‚ under basic conditions‚ involves the nucleophilic addition of an enolate ion to another carbonyl group. The resulting product‚ a beta-hydroxy ketone or aldehyde‚ is called an aldol because it contains both and aldehyde group and the hydroxy group of alcohol. Condensations‚ including aldol condensation‚ combine two or more molecules‚ typically with a loss of a smaller molecule (including
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1691 Strong 4. The reaction of the unknown with bromine gave a negative result meaning the solution did not turn clear‚ but rather‚ maintained an orangish brown color. This is interpreted to mean that bromine in not adding to either side of an alkene bond‚ so there is no C=C bond in the unknown compound. The reaction of the dicarboxylic acid with bromine gave a positive result meaning that the solution turned clear as a result of bromine adding to both sided of the C=C bond. The dicarboxylic
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C H A P T E R 5 Basic Concepts from Organic Chemistry 5.1 | INTRODUCTION The fundamental information that environmental engineers and scientists need concerning organic chemistry differs considerably from that which the organic chemist requires. This difference is due to the fact that chemists are concerned principally with the synthesis of compounds‚ whereas environmental engineers and scientists are concerned‚ in the main‚ with how the organic compounds in liquid‚ solid‚ and gaseous wastes
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Infrared Spectroscopy Organic Chemistry Lab 301A B. The purpose of this lab is to study Infrared Spectroscopy‚ which focuses on the study of the electromagnetic spectrum. The area to be studied is the infrared region‚ which is made up of gamma‚ X‚ and UV rays. We want to be able to identify spectra’s to their complementary structures. The background of this experiment particularly deals with the study of compound structure determination‚ and traits. We must be aware of the functional groups
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pigments found in plants are chlorophyll A‚ chlorophyll B‚ β-Carotene‚ lutein‚ neoxathin‚ violaxanthin‚ and phaeophtin. The most abundant of the pigments are chlorophyll A and chlorophyll B‚ the only Name of Class fast alkanes alkenes ethers halogenated hydrocarbons aromatic hydrocarbons increasing polarity aldehydes and ketones esters alcohols amines slow carboxylic acids General Formula difference between the two is that on ring 3 chlorophyll a has a RH R2C CR2 methyl group where chlorophyll
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