Enter. Insert the temperature probe in the ice water. Swirl the temperature probe until the temperature approaches and stabilizes near 0 *C (it may not read exactly 0 *C). Press Enter. 4. Remove the temperature probe from the ice water bath. 5. Press SetUp to establish scan parameters for the experiment. Press F1 to set the limits for the scan. Use the keys to move from min to max or from X to Y. An * marks the parameter selected to change at any given time. The Y-axis is for temperature
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the fix shaft between the gates. 2. Place a short strip of timer tape in the recording timer over the paper disc. 3. Make sure the tape is threaded through the gates and is free of snags. 4. Turn the timer on and pull the strip through the gates. 5. Make sure you are getting dots on the underside of the tape. 6. Use the test tape to decide on the best speed to pull the tape‚ so that the dots are easy to read. 7. Place a +1.5 meter piece of tape in the timer. 8. Pull the tape through a gentle
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Constituent of “Panacetin” Recrystallization& Melting-Point Measurement Organic Chemistry Lab Introduction: Panacetin purportedly includes sucrose‚ aspirin‚ and acetaminophen. However‚ the accuracy of Panacetin’s contents has been called into question by the Association for Safe Pharmaceuticals. Therefore‚ the lab must discover the accuracy of the ingredients listed on Panacetin’s label. The unknown in this experiment is presumed to be something
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Potatoes Lab #1 Purpose: To find the molarity/concentration of potato cytoplasm. Materials: As on page 1 in the lab handout. Procedure: As on page 1 in the lab handout. Data and Observations: Test Tube # | Concentration of sucrose solution (mol/L) | Initial Mass (g) | Final Mass | Percentage change in mass | 1 | 1.0 mol/L | 3.00g | 2.25g | -25.0% | 2 | 0.9 mol/L | 2.70g | 2.07g | -23.3% | 3 | 0.8 mol/L | 2.92g | 2.25g | -22.9% | 4 | 0.7 mol/L | 2.60g | 1.94g | -25.4% | 5 | 0.6
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Abstract: For the first part of this lab we refluxed different Carboxylic acids and alcohols in the presence of a acid catalyst in order to form Esters by Fischer Esterification. These Esters had different pleasant smells that we then evaluated. In the second part of the experiment‚ we broke the ester bonds of a triglyceride in order to form glycerol and carboxylate salts. This process is known as Saponification because it produces amphiphilic molecules that allow soap to remove dirt from the surface
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Ashley Robins 9/13/11 Honors Chemistry Period 4 Density Lab Purpose: 1. To determine the density of a solid using different laboratory techniques for measuring volume. 2. To use the intensive property of density to identify an unknown substance. Procedure: 1. Obtain a bag marked with a number containing a cube and a cylinder from the teacher. Record the number on the bag in the data table. Density of a cube: Using a balance‚ record the mass of the cube to the nearest tenth of a gram
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The Virtual Lab – ELISA Test Lab: Immunology 09/04/2013 Instructors: Dr. Charlie Wilson Written by: Dipen Patel I. Objective: The purpose of the lab was to learn the procedure of performing an ELISA test to determine whether a particular antibody is present in a patient’s blood sample. ELISA is an abbreviation for “Enzyme-linked Immunosorbent Assay." II. Introduction: The interaction of antigen and antibody outside the body can be used to determine if patient
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of Oxalate Ion in Ferric Oxalate Trihydrate using Titrimetry Abstract: In this two-part lab‚ we will learn about coordination compounds and their uses with stoiciometry. We will also find out about how theoretical yield is calculated from a reaction we will create. We will also synthesize Potassium Ferric Oxalate Trihydrate (K_3 [〖Fe(C_2 O_4)〗_3]•3H_2 O) using a two step reaction. In the second part of this lab we will calculate how much Oxalate Ion is present in the K_3 [〖Fe(C_2 O_4)〗_3]•3H_2 O using
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Animal Phyla Lab Adapted from “Phylum Lab” produced by the National Aquarium in Baltimore The diversity of animal life on Earth is astounding. Each animal has a unique body plan which allows it to survive and adapt to its given surroundings. With such an abundance of species‚ classifying animals into different categories is necessary. At first the diversity of animals can be overwhelming‚ but after further research and observation‚ many likenesses appear. These similarities become the basis for
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Lab 3 – Biodiversity Demonstration 1: Interdependence of Species Table 1: Interdependence of Species Results Round Species Missing (Bead Color and Name) 1 Blue / Humans 2 Red / Flowers 3 Yellow / Bees 4 N/A POST LAB QUESTIONS 1. Explain how the ecosystem was affected by the missing species for each round of the demonstration. a. Round 1 = Without humans then all progress cease to exist and everything will go in reverse. Humans run pretty much everything and if we just eliminated humans then only
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