seem to be caused by adverse drug reactions to medical drugs‚ according to research. On the contrary‚ Philippines don’t have a high risk of deaths that causes these because here in our country‚ we rely on those alternative medicines or herbal medicines. It is a lot cheaper but actually‚ it doesn’t have those therapeutic claims so it has a minimal assurance of being treated with the sickness. With these‚ we choose to use Western Medicines as well. Adverse Drug Reaction (ADR) is the response of our body
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Constant of an Unknown Ester Hydrolysis Reaction Abstract The experiments to follow determined that the equilibrium concentrations of the reaction: ester + water ↔ alcohol + acid‚ are equal to 0.0363 moles of ester‚ 0.2852 moles of water‚ and 0.0268 moles each of alcohol and acid. Using this information the equilibrium constant was determined to be 0.06938. 1. Introduction In this lab the equilibrium constant‚ Kc‚ for the acid catalyzed reaction between an unknown ester and water
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On what I have seen‚ the first experiment showed chemical reaction to be more specific‚ combustion. In the experiment the Potassium permanganate (KmnO4) was used as the oxidant‚ and obviously oil as the fuel. As the two were mixed they needed to release energy in form of heat‚ that’s where combustion occurs. I learn that Combustion is the sequence of exothermic chemical reactions between a fuel and an oxidant accompanied by the production of heat and conversion of chemical species. The release of
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Purpose: In this experiment I will predict the amount of product produced in a precipitation reaction using stoichiometry by accurately measuring the reactants and products of the reaction. I will also determine the actual yield vs. the theoretical yield by calculating the percent yield. Materials: 1 Distilled water 1 Paper towels 1 Small paper cup 1 Coffee cup or mug 1 Beaker‚ 100 mL‚ glass 1 Funnel 1 Cylinder‚ 25 mL 1 Goggles-Safety 1 Scale-Digital-500g 1 Weighing boat‚ Plastic 1 CaCl2·2 H2O-Calcium
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This experiment was a Landolt Iodine clock reaction - Oxidation of Bisulphite by Iodate. It involved conducting three measured experiments. The first variable tested was concencentration. This was tested by conducting two experiments‚ each varying the concentration of either the NaHSO3 or KIO3. The varying of NaHSO3 involved using 0.1 Molar of KIO3 against decreasing concentrations of NaHSO3 (0.25 M‚ 0.125 M‚ 0.0625 M and 0.03125 M). When decreasing the concentration of KIO3‚ 0.25 M of NaHSO3 was
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purpose of this lab was to find the theoretical and experimental percentage yields of the double displacement reaction between the solutions Lead (II) Nitrate (PbNO3) and Potassium Iodide (KI). It is important to obtain amounts of Lead (II) Nitrate and Potassium Iodide as close to 1.44g as possible. This reaction creates Lead (II) Iodide and Potassium Nitrate. The precipitate during this reaction is Lead (II) Iodide. The balanced equation is Pb(NO3)2 + 2KI= PbI2 + 2KNO3. In this lab the Lead (II) Iodide
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Top of Form 1. What is the pH of a buffer that results when 33 g NaHCO3 is mixed with 100.0 mL of 2.50 M NaOH and diluted with water to 250 mL? (Ka for HCO3- = 4.8 10-11) (Points : 10) 8.20 10.07 10.12 10.32 10.56 2. What is the pH of an aqueous solution of 0.30 M HF and 0.15 M F-? (Ka of HF = 7.2 10-4) (Points : 10) 1.83 2.84 3.14 3.44 10.86 3. Which of the following mathematical expressions
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Ch.5 Yield (total return) = Dollar inc + (end-beg) beg. Value Risk of Return = r= Risk Free rate + Risk Prem r=rRF+DRP+LP+MRP Risk Free Rate = rRF = r* + IP -effects of int rates on PV/Price of securities: int goes up‚ value of bonds goes down‚ stock goes down (NPV) Prices -factors that influence int rates/yield curve 1.production opportunities-return avail w/in an economy from inves. In productive asset; higher prod opp‚ higher return 2. Time preferences for consumption 3
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Prof. K. M. Muraleedharan Aromatic electrophilic substitution (Ar-SE) Reactions The special reactivity of aromatic systems towards electrophiles arises mainly from two factors: the presence of π electron density above and below the plane of the ring - making it nucleophilic‚ and the drive to regain the aromatic character by opting for substitution as opposed to a simple addition reaction. Preference towards addition reactions in the case of alkenes and substitution in the case of aromatic compounds
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to determine the rate constants‚ k1‚ for the methyl acetate hydrolysis reaction at 25 °C and 35 °C‚ as well as the overall activation energy of the reaction. Methods Methyl acetate was placed in an HCl solution‚ in which it reacts with water to form acetic acid over time. At each time interval‚ an aliquot of the mixture was removed for titration against NaOH to determine the concentration of the acetic acid produced. From the amount of acetic acid produced overtime‚ the rate constant‚ k1‚ can
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