Reaction of Anthracene with Maleic Anhydride 1 The Diels-Alder Reaction of Anthracene with Maleic Anhydride Microscale Diels-Alder Reaction Leah Monroe March 6‚ 2003 Organic Chemistry Lab II Experiment performed on February 25 and 27‚ 2003 Abstract: This experiment involved a reaction between anthracene and maleic anhydride via a Diels Alder reaction to yield 9‚ 10-dihydroanthracene-9‚10-α‚ β-succinic anhydride. Anthracene was the diene and maleic anhydride was the dienophile. The percent
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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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Abstract For the following experiment‚ a Diels-Alder reaction between maleic anhydride and anthracene was conducted. Reflux mechanism was used for the reaction to occur. To increase the speed of the reaction‚ xylene was used because of its high boiling point. After the reaction was complete‚ 1.08g of the off white product was obtained with a yield of 69.7%. It was not clear if a pure product had been formed because time constraints did not allow us to perform thin layer chromatography. Introduction
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Diels-Alder Synthesis of Exo-Norbornene-cis-5‚6-Dicarboxylic Anhydride for Organic Chemistry Laboratory Instruction Kyle Myers and Dr. James Roark University of Nebraska at Kearney‚ Department of Chemistry‚ Kearney‚ NE 68849 Abstract A technique for the Diels-Alder synthesis of endo-norbornene-cis-5‚6dicarboxylic anhydride and its stereoisomer‚ exo-norbornene-cis-5‚6-dicarboxylic anhydride‚ is explained. To prove that each stereoisomer was made in the experiment and to distinguish between the
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electronic components‚ printed circuit boards‚ consumer electronics and other industrial products. This report focuses on analyzing photoresist & its special chemicals and capacitor chemicals as well as maleic anhydride derivatives used in printed circuit boards‚ flat panel displays and semiconductors. 1 Photoresist Photoresist is mainly used for fine graphics processing in PCB‚ LCD‚ semiconductor and other areas. In 2013‚ the global photoresist market scale reached approximately RMB40 billion‚ mainly
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Ronak Parikh U30682934 Experiment 2: Diels-Alder Reaction: Synthesis of cis-Norbornene-5‚6-endo-dicaroboxylic anhydride Introduction: The main goal of this experiment is to perform a Diels-Alder reaction between 2‚3-dimethyl-1‚3-butadiene and maleic anhydride‚ identify the product and hydrolyze to form the dicarboxylic acid. Diels alder reactions are classified as pericyclic reaction‚ which is a reaction which involves a cyclic rearrangement of bonding electrons‚ which means
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Diels-Alder Reaction: Synthesis of cis-Norbornene-5‚ 6-endo-dicarboxylic anhydride Introduction: The Diels-Alder reaction is a [4+2] cycloaddition of a conjugated diene and a dienophile. This type of reaction was named for Otto Diels and Kurt Alder who were the first to investigate this reaction (Weldegirma‚ 2012). The Diels- Alder reaction is one of the most important reactions in all of organic chemistry because of the applicability of it. This reaction can form
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Written in the first chapter of the Book of Genesis 1:1-31 through to Genesis 2:1-3‚ is the most popular Hebrew and Christian version of the Creation story. To begin with‚ in the first day God creates heaven‚ Earth‚ day and night. Then on the second day the skies and oceans are created followed by the creation of dry land‚ vegetation and fruit trees on the third day. Continuing on the fourth day God creates the sun‚ moon‚ stars and then on the fifth day all creatures that swim along with all creatures
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Score: 139.70 1. out of 140 points (99.79%) award: 10 out of 10.00 points Exercise 3-1 Classifying adjusting entries LO C3 In the blank space beside each adjusting entry‚ enter the letter of the explanation A through F that most closely describes the entry. A. B. C. D. E. F. To record this period’s depreciation expense. To record accrued salaries expense. To record this period’s use of a prepaid expense. To record accrued interest revenue. To record accrued interest expense. To record the earning
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Centre for Foundation Studies Foundation In Science Year 1 Trimester 1 Unit Code Unit Title Session : : : FHSC1114 Physical Chemistry 2015/05 : Ms. Amelia Chiang‚ Ms. Azlina Banu‚ Ms. Farhanah‚ Ms.Gurpreet‚ Ms. Jamie‚ Ms. Lau Mei Chien‚ Ms. Lily Lee‚ Ms. Nabilah‚ Mr. Ng Sweet Kin‚ Ms. Phang Ying Ning‚ Ms. Precilla‚ Ms. Rachel Tham‚ Ms. Rajalakshmi‚ Mr. Sivabalan‚ Ms. Tan Lee Siew Tutorial 3: Chapter 3 Stoichiometry and Solution Concentration 1. Balance the following equations: (a) (b) 2. V2O5(s)
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