Chem. 317 Title: The Synthesis of Chloropentaamminecobalt(III) chloride and Linkage Isomerization to Further Synthesis Pentamminenitrocobalt(III) chloride Experimental: Ammonium chloride (.0467 mol) was diluted in concentrated aqueous ammonia (15 ml) in a 125ml Erlenmeyer flask. CoCl26H2O (.0210 mol) was then added to the ammonium chloride solution. The ammonium chloride solution was heated and stirred while 30% hydrogen peroxide (4 mL) was added drop wise. The reaction was monitored and removed from the heat once the effervescence ceased, and then was allowed to cool.
In the first part, five 100 mL flasks of 5 mL ligand solution, 5 mL 2 M sodium acetate, 4 mL 3 M NH2OH, and 1-5 mL Fe2+ solution are diluted with water. The absorption spectrum for varying concentrations of Fe2+ are measured using a spectrophotometer and the data is graphed in Excel. The slope of the line is ε in the Beer-Lambart equation A = εcl. In the second part of the experiment, eleven flasks containing diluted stock solutions of Fe2+ and ligand are mixed with 5 mL 2 M sodium acetate and 4 mL 3 M NH2OH and diluted with water. The absorption spectrum is measured using a spectrophotometer and the data is graphed in Excel.
Reactions Lab David Vaghari INSTRUCTOR: Dr. Chernovitz Monday, July 23, 2012 Oxygen Production Introduction In this lab, potassium chlorate will be decomposed producing oxygen gas and potassium chloride. The hypothesis is that the reaction will yield 3.916 grams of oxygen gas. Materials Test tube 10 grams potassium chlorate Bunsen burner Procedure Step 1. Obtain a test tube, place a 10 gm of potassium chlorate. Step 2.
The supernatant was transferred to a 1.5 ml tube; to which 225 µl of 5 M NH4Ac was added, mixed gently, incubated on ice for 30 min and centrifuged at 10,000 rpm for 15 min at 4°C. Then the supernatant was transferred to a fresh tube, 510 µl of isopropanol was added to precipitate the DNA and centrifuged immediately for 10 min at 10,000 rpm. The supernatant was removed; the pellet was washed twice with cold 70% ethanol, air-dried and suspended in 50 µl TE
Discussion and Conclusion In this experiment, the bromination of an alkene will be observed and a mechanism to account for the occurrence distribution of the products will be determined. In the first part of the experiment the 0.9 grams of E-stilbene will be put in a flask with 10ml of dichloromethane and then stirred to affect dissolution of the E-stilbene, since dichloromethane is a nonpolar solvent which can dissolve the nonpolar alkene. After the E-stilbene has been dissolved, 5ml of bromine in dichloromethane will be added, which will be stirred for thirty minutes until the solution is white, to ensure that the reaction has gone to completion. Bromine in dichloromethane is used because dichloromethane works as a good solvent for bromination reactions, due to the fact that it doesn’t react with bromine or most other organic molecules. The reddish color of bromine is discharged upon addition to an alkene as the bromine reacts, making this reaction a useful qualitative test for unsaturation when the reaction has gone to completion.
The blends were preheated for 1 min in a hot press (Toyoseiki, Japan) and then compression molded at 190℃ for 5 min under 25 bars pressure. After that, the samples were cooled to room temperature under the same pressure and sheets with 1 mm thickness were obtained for experiments. Samples are coded as P-xD-yPO, in which x and y demonstrate the
Solution Stoichiometry and Gas Law Problems Problem 1 In flask A, 1.500g of silver nitrate solid is dissolved in 50.0mL of water, while in flask B, 0.500g of potassium carbonate is dissolved in 25.0mL of water. The two solutions are then mixed together. a) Before mixing, what is the molarity of each solution? b) Write the balanced molecular equation, the complete ionic equation, and the net ionic equation for the reaction. c) If the percentage yield is 85.0%, what mass of precipitate is actually produced?
Part A: Spectroscopy 1. 0.05g of Iron(III) Nitrate in a 50-ml beaker. Add 17 mL of distilled water to the beaker and mix with a stir rod until the solid is completely dissolved. 2. Obtain another 50-mL beaker and add 0.05g of Chromium(III) Nitrate to the beaker.
Add a quarter spatula of copper (II) oxide and warm the solution gently to the 4th test tube and record observations. 7. To the 5th test tube, add 3cm3 of ethanol a couple of drops of conc, sulphuric acid and warm gently. Pour the resulting mixture into 30cm3 of sodium carbonate solution to remove excess acid and smell and record observations. Experiment 2 Time | Observations | 5 minutes | Bubbled like sugar | Once salt water was added | Turned soapy white and thick | Equation: METHOD 1) Put 2 cm3 of castor oil into a 250 cm3 beaker and add 10 cm3 of 5mol.dm-3 sodium hydroxide from a measuring cylinder.
EXPERIMENT ( 3 ) Topic : The preparation of Phenyl Benzoate from benzoyl chloride Introduction : The preparation of phenyl benzoate (ester) from phenol and benzoyl chloride is an esterification. In this experiment, you are requested to prepare and purify phenyl benzoate by some techniques. Chemicals : Phenol, Benzoyl chloride, Dilute NaOH, Methanol Procedures : 1. Dissolve 1 g phenol in 15 cm3 dilute NaOH using a 50 cm3 quickfit flask. 2.