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    Lifesaver Lab

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    coloring. The purpose of this laboratory is to demonstrate in which solution the LifeSaver dissolves faster within five minutes. Materials Water Salt Baking Soda Regular LifeSaver hard candy Cups Watch settled for 5 minutes Observations The Lifesavers are round shape‚ purple color‚ solid and hard and 2cm size. Water is clear at room temperature. Salt and Baking Soda are in it solid state with power appearance. Question Which solution will dissolve the LifeSaver the most within five minutes? Hypothesis

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    Experiment 1 Mixtures

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    Experiment 1: Mixtures Aim: To develop an understanding of different types of mixtures including solutions and to examine the different solubilities of some solutes in two solvents: water and ethanol Procedure: Refer to Experiments Book Pg 13 Results: Part A- Mixture Observations Classifications 1 100% Orange Juice There were suspended pulp in the juice Heterogeneous Mixture 2 100% Apple Juice Clear solution Homogeneous Mixture 3 Solder Uniform mixture Homogeneous Mixture 4 Fruit Cake Chunks of raisins

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    An isotonic solution has the same osmolarity as a tissue. A hypertonic solution has a higher osmolarity and a hypotonic solution has a lower osmolarity. If samples of a tissue are bathed in hypertonic and hypotonic solutions‚ and measurements are taken to find out whether water enters or leaves the tissue‚ it is possible to deduce what concentration of solution would be isotonic and therefore predict the results of osmosis in different

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    Diffusion

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    called hypotonic solution and hypertonic solution. Hypothesis: My Hypothesis for diffusion that the starch solution will be hypotonic and diffuse into potassium iodide (IkI). Hypothesis for osmosis is that each of the individual dialysis bags will increase because of the different concentration of the solutions. Which makes this and hypotonic experiment. Hypothesis for this experiment is that each of the four cylinders of potato will decrease in mass‚ because of the solution/concentration

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    Biology Osmosis

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    the effect of osmosis In potato cells Introduction I am doing an experiment to find out the effect that osmosis has on Water solution and a Sugar solution. Osmosis is a process which water moves from an area of low concentration to an area of high concentration. I am going to record my results to see if osmosis occurs in water solution of sugar solution. Apparatus In this experiment I would need; - 1) 3 test tube 2) A beaker 3) A cork borer 4) A Knife Safety

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    moving in one direction equals to the amount of molecules moving in the other direction. There are three types of solutions to diffusion: isotonic‚ hypertonic‚ or hypotonic. When the solutions have the same concentration of solutes‚ they are isotonic. When the solutions differ in their solute concentration‚ the solution with more solute is hypertonic to the other solution. The solution that has less solute is hypotonic

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    to determine the equilibrium constant for the reaction Fe3+(aq) + HSCN(aq) –>FeSCN2+(aq) + H+(aq). The equilibrium constant expression Kc for Reaction is kc=FeSCN2+[H+]Fe3++[HSCN] Procedure *Preparation of the Beer’s law plot Prepare five solutions of FeSCN2+(aq) of known concentrations between 1x10-5M and 1x10-4M by diluting various volumes of 4.62x10-4 HSCN. Calculate the Final concentration FeSCN2+ for Beer’s law Using the C1V1=C2V2 Initial Concentration (M) | Initial Volume(ml) | Final

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    Ph Measurer Lab Report

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    conduct my experiment‚ I measured 10g of ascorbic acid powder and mix it within 1 litre of water. I believed that by having the solution prepared before putting in the d-block elements would save time overall. Unfortunately‚ the data was all over the place‚ this is because the later I conduct the experiment‚ there is a higher chance of oxidation occur in the ascorbic acid solution as it have a direct contact with oxygen in the atmosphere. In order to keep constancy‚ I had to reduce the amount of ascorbic

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    buffer was made. We began this experiment by measuring seven constant amounts of 1ml of 0.1% catechol using a 1 mL pipet into each seven cuvettes. The catechol is our substrate solution. Next‚ different amounts of phosphate buffer ph.6 of 0.5ml‚ 1.0ml‚ 1.5ml‚ 2.0 ml 2.5ml‚ 3.0ml and 4.0ml were added to each of the solution of the 0.1% catechol. The purpose of adding phosphate buffer pH6 is to maintain the particular ph6 for the polyphenol-oxidase (enzyme)‚

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    was first determined. Acetanilide was produced by acetylation of aniline with acetic anhydride. The crude acetanilide was dissolved in a solvent in a heating water bath. The hot solution was filtered and the filtrate‚ cooled slowly in an ice bath as crystals started forming out. As the compound crystallizes from the solution‚ molecules of other compounds were excluded from the crystals to obtain pure acetanilide. INTRODUCTION Recrystallization‚ referred to as the second crystallization‚ is a method

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