A total of 0.1 ml of supernatant was added to cuvette containing 1.9 ml of 50mM phosphate buffer (pH 7). The reaction was started by the addition of 1 ml freshly prepared 30mM H2O2. The rate of decomposition of H2O2 was measured spectrophotometrically at 240 nm. Catalase values were expressed as n moles H2O2 consumed/min/mg protein. Measurement of lipid peroxidation TBARS, a measure of lipid per oxidation, was measured as described by Ohkawa .
One of the reactions you observed resulted in this product: NaCl + H2O + CO2 (g)? What well did this reaction occur in? Describe how the observations for this reaction support your answer. B BoldI ItalicsU Underline Bulleted list Numbered list Superscript Subscript70 Words A reaction I observed in number 1.) Sodium Bicarbonate mixed with Hydrochloric acid.
The theoretical yield for Zinc Sulfide is 0.49 grams but the actual yield is 0.38 grams. So if 0.38 is divided by 0.49 and multiplied by 100 then the percent yield for Zinc Sulfide would be 77.6%. When it comes to Sodium Chloride, the theoretical yield is 0.58 grams and the actual yield is 0.45 grams. So when 0.45 grams is divided by 0.58 grams and multiplied by 100, the percent yield would be 77.5% of Sodium chloride. The actual yield is directly taken from the mass of the products in the experiment while the theoretical yield is determined by using stoichiometric calculations.
Title : Determination of chemical formula of hydrate Aim To determine the chemical formula of hydrated Copper (II) sulphate, CuSO4 Research Background “When the chemical is heated the hydrate will convert to an anhydrous ionic compound (this means the water will leave it). The moles of H2O will be determined by assuming the amount of mass lost by heating is the mass of the evaporated H2O. The moles of the CuSO4 (the white substance after heating) can be calculated from the mass of the white crystals. Using the molar ratio of moles of CuSO4 to moles of H2O, one can determine the chemical formula of the hydrate.” Apparatus and materials Apparatus and Materials used Quantity Crucible and lid Tripod stand Clay triangle Wire gauze White tile
From the bromination of 0.05g aniline, 0.156g of the product was collected. The percent yield was calculated to be 88.1%. Some amount of the product was lost when transferring the product from the Buchner funnel to the balance to measure its mass. To ensure the formation of the desired product, melting point of the product was measured to be 119.8-121.90c, which is in the range of the normal melting point of 2,4,6-tribromoanilne, 120-1220c. Thus, the product was indeed
The goal of the experiment is to synthesize a bromohexane compound from 1-hexene and HBr(aq) under reflux conditions and use the silver nitrate and sodium iodide tests to determine if the product is a primary or secondary hydrocarbon. The heterogeneous reaction mixture contains 1-hexene, 48% HBr(aq), and tetrabutylammonium bromide and was heated to under reflux conditions. Heating under reflux means that the reaction mixture is heated at its boiling point so that the reaction can proceed at a faster rate. The attached reflux condenser allows volatile substances to return to the reaction flask so that no material is lost. Since alkenes are immiscible with concentrated HBr, tetrabutylammonium bromide is used as a phase-transfer catalyst.
Linoleic acid peroxidation was initiated by the addition of 4 mM FeSO4.7H2O, incubated for 60 min at 37oC and terminated by the addition of 2 mL of ice cold trichloroacetic acid (10% v/v). An amount of 1 mL of thiobarbituric acid (1% w/v in 50 mM NaOH) was added to 1 mL of the reaction mixture, followed by heating at 95oC for 60 min. The reaction sample was read at 532 nm.7 The percentage of linoleic acid peroxidation inhibition activity was calculated using the following equation: % Inhibition = [(AB - AA)/AB] x 100, where AB, absorption of blank sample, AA, absorption of test sample. 2.5.4. Metal chelating activity Briefly, 2 mM FeCl2 was added to different concentrations of test sample and reaction was initiated by the addition of 5 mM ferrozine.
of the sugar in the green compact was dissolved in water. When the percentage of the dissolved sugar exceeded 70% wt. inadequate or discontinuous carbon coating on the Al-foam was observed. When the percentage of the dissolved sugar was less than 60% wt. then partial collapse of the foam structure was
1 Experiment 7: Titration of an Antacid Objective: In this experiment, you will standardize a solution of base using the analytical technique known as titration. Using this standardized solution, you will determine the acid neutralizing power of a commercially available antacid tablet. Introduction An understanding of the properties of acids and bases is an essential part of understanding chemical reactions (see Tro, pp 167-171). In aqueous solutions, a compound that produces H+ ions upon dissolution is termed an acid. A compound that produces OH– ions when dissolved in water is called a base.
The electrochemical behaviour of copper-1,10-phenanthroline (phen) complex in aqueous and in water-acetone mixed solutions was studied by CV-thin layer spectroelectrochemistry. In aqueous solution, [Cu(II)(phen)2]2+ complex electrochemically reduced to [Cu(I)(phen)2H2O]+ with maximum absorption at 405nm, and followed by a reversible chemical reaction. The formal potential, E0=0.078V, the number of electron transferred, n=1.0, and the equilibrium constant of the following chemical reaction, K=0.107 (0.005), were determined. In water-acetone mixed solution, [Cu(II)(phen)2]2+ reduced to [Cu(I)(phen)2]+ with maximum absorption at 435 nm. Keywords: CV-thin layer spectroelectrochemistry; copper-1,10-phenanthroline complex 1.