Formalin – positive * Glucose – positive * Benzaldehyde * Acetone * Sodium Nitroprusside Test – Test for presence of acetone * -Wine red solution * Iodoform Test – Test for Methyl Ketones * Acetone – positive * Ethyl methyl ketone – positive * Ethyl acetate * Special test for Benzaldehyde * Formation of crystals * Molisch Test – General test for Carbohydrates * Violet ring (2nd layer) * Glucose
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hypothesized the final ester would be octyl acetate. For test tube C I hypothesized it would be methyl salicylate. For test tube D I hypothesized it would be isopentyl acetate. Materials and Methods Apparatus 4 test tubes Test tube rack Graduated cylinder (10 mL) 150 mL beaker 250 mL beakers (2) Hot plate Thermometer Safety glasses Beaker tongs Test tube holder Reagents Methanol Methyl-2-propanol 1-pentanol 1-octanol Acetic acid Formic acid (methanoic acid) Salicylic acid
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(3)NMRQuestion 1 1 / 1 point Equivalent protons in a molecule will result in one NMR signal. How many NMR signals would you predict for each of the following molecules? __1__ benzene __2__ 3-pentanone __4__ toluene __3__ ethanol __2__ t-butyl methyl ether 1. 1 2. 2 3. 3 4. 4 Question 2 1 / 1 point A compound to be analyzed by NMR should be dissolved in a solvent. Clearly the solvent should not have an NMR signal in the spectral area you are trying to analyze. Which solvents are appropriate
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Alkane‚ Alkene‚ Alkyne & Aromatic Learning Objectives 1. 2. 3. Determine the IUPAC name‚ common name and structure of an alkanes‚ alkenes and cycloalkanes. Identify the physical properties of alkanes. Describe briefly natural sources and importance of alkanes Describe reactions of alkanes Propose a mechanism on free radicals substitution 4. 5. 6. Describe the preparation and reactions of alkenes. 7. Propose mechanism on preparation; dehydration of alcohol 8. Define carbocation
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2-(2‚4-Dinitrobenzyl) pyridine Peter Defnet and Cody Krepps Department of Chemstry Juniata College Huntingdon‚ PA September 18‚ 2012 Abstract: Nitration of 2-benzylpyridine is supposed to yield 2-(2‚4-Dinitrobenzyl) pyridine‚ when electrophilic aromatic substitution is the mechanism. Experiencing many pitfalls‚ however‚ has lead to the actual product obtained to contain the expected product‚ as well as many impurities. This report examines the supposed mechanism for the electrophilic substitution
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Conclusion: ¬¬The goal of the first part of this experiment was to achieve a 50-50 conversion of fluorene to Fluorenone. In order to achieve the goal of the experiment fluorene was oxidized to Fluorenone. The hydroxide ions from the sodium hydroxide in the presence of Stark’s catalyst would be able to de-protonate the acidic fluorene protons. This would result in the formation of a carbanion which attacks the oxygen from the air resulting in the formation of a hydroperoxide and eventually a ketone
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The present invention relates to polyvinyl chloride plastisol compositions‚ for example sealant compositions. In the manufacture of automobiles‚ the automobile body is initially primed with a coating composition to prevent corrosion of the metal. This can be done in a number of ways although generally it is performed by cationic electrodeposition using the auto body as the cathode. Once the automobile body has been primed in this manner‚ subsequent steps in the assembly are carried out. These
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Susceptible to both nucleophiles and electrophiles Presence of C=O TEST FOR ALDEHYDES AND KETONES - - Reaction with 2‚4-DNP (Dinitrophenylhydrazine) Positive: Formation of yellow precipitate IODOFORM TEST - Carbonyl compounds: Methyl ketones will give a positive result Postive: Yellow precipitate (CHI3) MOLISCH’S TEST for carbohydrates - TOLLEN’S TEST – for aldehydes - - Test for easily oxidizable compounds (ex. Aldehydes) Positive: Silver mirror deposit -
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Extraction and analysis of two compounds from unknown solution C ABSTRACT Liquid C and solid C were both extracted from unknown solution by first using chemically active liquid-liquid extract‚ followed by vacuum filtration. Liquid C and solid C were then purified with the use of simple distillation and recrystallization respectively. Through the process of recrystallization‚ the percentage purity of solid C was found to be 6.01%. The melting point range of purified solid C was 117.0 – 119
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Experiment Date: 3/12/2012 Photochemistry: Photoreduction of benzophenone and rearrangement to benzpinacolone Abstract: In this experiment Benzpinacolone was synthesized in a process that contained two steps. First the photoreduction of benzophenone in 2-propanol‚ which was done by placing the flask under sunlightfor the absorption of the UV rays to carry out the reaction. Then the second part was the dehydration of benzpinacol to benzpinacolone‚ where the benzpinacol product was converted
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