Acid-Base Titration Using a pH Meter Bradley Holloway and Jennifer Parker Period 6 April 16‚ 2013 Introduction: In chemistry‚ the ability to find molarities of acidic and basic solutions is a convenient way to convert between moles of solute and the volumes of their solutions. Through the process of titration‚ the molarity of these acids and bases can be found to a high level of precision. To begin titration‚ one solution is added to a second solution slowly until a certain point
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brands of calcium carbonate (CaCO3) tablets was determined by reacting the tablets in excess standardized hydrochloric acid (HCl) and then back-titrating with a standardized sodium hydroxide (NaOH) solution. Back titration was required for two reasons. Firstly‚ CaCO3 tablets are poorly water-soluble but dissolve rapidly in acid. Secondly‚ CaCO3 is a weak base so it is difficult to determine the end point of the reaction if titrated directly. Assuming good manufacturing practice‚ the amount of active
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hydrated iron (II) ammonium sulfate is weighed accurately using a 50mL beaker. The salt is transferred to a 250mL volumetric flask using a filter funnel‚ washed down with distilled water. The container is rinsed carefully and the rinsing is added to the volumetric flask. 100mL of water is added slowly to the volumetric flask‚ followed by 5mL of concentrated H¬2SO4. It is stoppered‚ shaken well and made up to the mark with distilled water. Standardizing Potassium Permanganate Solution The
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Experiment 2 Title: Determination of Quinine in Tonic Water Objective: To Determine the Concentration of Quinine Hydrochloride in Sample (Schweppers) given‚ by plotting a Calibration Curve of Fluorescent Intensity against Concentration of Quinine Hydrochloride in ppm‚ after Fluorescence Intensity of a series of Standard Solution prepared and the Sample solution by Fluorescence Spectrometer. Data: Brand name of tonic water sample: Schweppes Dilution factor = 1000 Concentration of
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The inverted water method MLA citation BBC News. BBC‚ n.d. Web. 09 Nov. 2015. "Factors Affecting Enzyme Activity." Factors Affecting Enzyme Activity. N.p.‚ n.d. Web. 14 Nov. 2015. Enzymes. Scenario experiment AIM: To investigate one factor that affect the distribution of hydrogen peroxide by the catalase in this organism. In this catalase and hydrogen peroxide experiment‚ we will find out how enzymes act as catalysts by causing chemical reactions to occur. Using a potato and hydrogen peroxide
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BACK TITRATION- DETERMINATION OF THE CARBONATE CONTENT IN GARDEN LIME NAME: OSEI BONSU ERIC ID: 3906409 EXPERIMENT: I.2.2.1.
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Example Lab Report Experiment 4 1. Judith Anthony‚” Strong Acid/Strong Base Titrations”‚ CHEM 1130‚ T.A-Joseph Kreft‚ Tuesday 8am‚Room 1871‚Donna Ellitnorpe. 2. Purpose of this experiment: The purpose of this experiment is to observe the neutralization reaction that occurs between strong acid and strong base solutions. The technique of titration is used to observe the acid content of the fluid in a car battery. 3. Procedure: Calculate the volume of 6.00 M NaoH that is needed
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D. F. Nachman Thermochemistry: An Ice Calorimeter Determination of Reaction Enthalpy 9/11/2014 Introduction: A chemical reaction often indicated by a transfer of energy measured in heat. By measuring this heat transfer in a constant pressurized environment‚ the enthalpy of the reaction can be used to infer certain information about a specific reactions reactants and products. The transfer of heat from outside sources in would be described as an endothermic reaction. Contrary‚ when
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Sacramento tap water reveals ion concentrations of various different dissolved minerals such as calcium (Ca2+) and magnesium (Mg2+). These concentrations are a result of mineral deposits in local lakes and rivers. Perma Pure‚ a gas conditioning products manufacturing company‚ simplifies the mechanism of ion exchange by explaining that water is a solvent that dissolves most ionic bonds when exposed to compounds ("The Mechanism of Ion Exchange"). Therefore‚ as tap water passes through rocks it will
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upstream and downstream fragments‚ 200 ng of pyrG marker fragment and adjust to 50 μL of double-distilled water. 35. Lysis Buffer: to prepare 50 mL of buffer dissolve 23.6 g of Guanidine thiocyanate (118.16 g/L) in 25 mL of double-distilled water. Once dissolved add: 2.5 mL of 1 M Tris-HCl pH 7.0 (121.14 g/L)‚ 2 mL of 0.5 M EDTA pH 8.0 (186.12 g/L) and 0.05 mL of Triton X-100. Add double-distilled water to 50mL (final concentrations: 4 M guanidine thiocyanate‚ 50 mM Tris-Hcl pH 7.0‚ 20 mM EDTA and 0.1
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