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    Synthesis of Co(Acac)3

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    submitted: 05/09/05 Chem 2130-3 Experiment 3: Synthesis of Co(acac-NO2)3 Introduction In this lab‚ Co(acac·NO2)3 is synthesized using the Co(acac)3 complex produced in Experiment 2. The Co(acac)3 complex is used as a reagent instead of acacH because acacH cannot be directly converted to 3-nitroacetylacetone. Since Co(acac)3 is not stable in HNO3‚ Cu(NO3)2 and acetic anhydride are used in this reaction to produce the final product‚ Co(acac·NO2)3. The exact mechanism of the

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    Acac

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    Reading effectively for assignments Anna Phillips anna.phillips@acu.edu.au Academic Skills Unit‚ MacKillop Campus Outline 1. Reading and note-making in different contexts 2. Reading critically and evaluating sources 3. Analysing the assignment and beginning research 4. Reading for the assignment Part 1 Reading and note-making in different contexts 1. Your reading strategies Techniques for reading Techniques for finding • Novels • A place to rent • Newspapers – Read fairly closely

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    3-Nitrochalcone Synthesis

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    objective of this experiment was to synthesize 3-nitrochalcone from 3- nitrobenzaldehyde. This was accomplished with a Diels-Alder reaction that utilized 3-nitrobenzaldehyde and acetophenone. After the reaction was completed‚ purification of the product was conducted using semi-microscale recrystallization. The melting point of the product was 136-141 oC‚ which is in the close vicinity of the literature melting point of 146 oC. The theoretical yield of 3-nitrochalcone was 0.253g and the yield after

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    Abstract This experiment is about the synthesis of 3-nitrobenzaldehyde through nitration. The nitration of benzaldehyde is an example of an electrophilic aromatic substitution reaction‚ in which a proton of an aromatic ring is replaced by a nitro group. Many aromatic substitution reactions are known to occur when an aromatic substrate is allowed to react with a suitable electrophilic reagent‚ and many other groups besides nitro may be introduced into the ring. Although the reaction produced a low

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    In this experiment‚ 5.281g of trans isomers of [Co(en)2Cl2]Cl was synthesized from 12.249g of CoCl2▪6H2O. First‚ CoCl2▪6H2O was reacted with ethlenediamine (NH2CH2CH2NH2) that formed [Co(en)2(H2O)2]Cl. Then the [Co(en)2(H2O)2]Cl was reacted with H2O2 to change the cobalt’s charge to cobalt(III) from cobalt(II). Finally HCl was added into the solution to form [Co(en)2Cl2]Cl. The percent yield was 45.51%.To synthesis trans isomers of [Co(en)2Cl2]Cl‚ distilled water was first mixed with CoCl2▪6H2O‚

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    The Grignard Synthesis of 3-methyl-3-heptanol In this experiment‚ an example of an organometallic compound which has a carbon magnesium bond will be utilized to form a tertiary alcohol. Grignard reagents have been extremely useful in the synthesis of a large number of classes of organic functional groups. Although Grignard reagents are unstable and decompose in air and moisture‚ they can be prepared and used immediately with moderate difficulty in the undergraduate organic chemistry laboratory

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    Synthesis

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    Synthesis The idea of gender wage discrimination being widely practiced in the United States today is a difficult concept for many to swallow. With the Equal Pay Act of 1963 and Title VII of the Civil Rights Act of 1964‚ the realization of the existence of the gender wage gap surprises many Americans. These authors bring to the forefront the idea that there is more to the gender wage gap then just companies discriminating against women and minorities. They sight many sources with defined data

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    stereochemistry of 2‚3-dibromo-3-phenylpropanoic was 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

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    Synthesis of a

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    I. INTRODUCTION Synthesis Acetylsalicylic acid is an acetyl derivative of salicylic acid which appears as a white and crystalline and a weakly acidic substance with a melting point of 135°C and is also known to be aspirin. It is one of the most widely used drugs that can lower fever and is used as a painkiller. According to (Escobel‚ 2011)‚ Aspirin is synthesized through the reaction of salicylic acid with acetyl anhydride that causes a chemical reaction that turns salicylic acid’s hydroxyl group

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    CHM1002 Synthesis of Benzanilide and Methyl 3-Nitrobenzoate and the Identification of ‘Unknowns’ from Spectroscopic and Physical Properties James Lucas 10394308 23/11/12 Introduction In this series of practicals it was the aim to synthesise both Benzanilide and Methyl 3-Nitrobenzoate. Benzanilide was synthesised using The Schotten Baumann reaction which takes a hydrogen atom from an amino group and substitutes it for an acyl group. For Methyl 3-Nitrobenzoate‚ NO2+

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