Experiment N | Kinetics of the Depolymerization of Diacetone Alcohol via Basic Catalysis | | Ingrid Tafur -5672578 | 2/11/2011 | CHM233O Partner: Laura Marrongelli Demonstrator: Cheryl McDowall Objective The rate constant of the depolymerization of diacetone alcohol via basic catalysis was determined by monitoring the change in volume as a function of time at constant temperature of a pseudo first order reaction where the species in excess was sodium hydroxide. This was accomplished
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cheese. Lactic acid bacteria(LAB)‚ a bacteria that can be found in the production of cheese‚ its stress gene was investigated in the experiment by using various biochemical and genetic techniques to identify and extract. The characterisation of the strain illustrates how identification of strains differ using different methods‚ such as gram stain and 16s rRNA screening. After the characterisation‚ the stress gene isolation assist the further understanding of the gene on LAB be giving different stress
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substrate concentration‚ the enzyme is working at “maximum efficiency.” With a concentration at 40‚ it produced 2‚339 products. 2. The maximum velocity of a reaction is reached when the active sites are almost continuously filled. Increased substrate concentration after this point will not increase the rate. The reaction rate increases as substrate concentration is increased. It will soon level off though. 3. When the concentration is at low substrate‚ most of the enzyme molecules are not filled
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Lab #5: Refraction of Light Theory: Refraction can be defined as the bending of a wave when it enters a medium which causes it to have some reduced speed. In terms of light‚ refraction occurs when the ray passes through some medium which slows its speed; such as water or glass. In this instance the ray tends to bend towards the normal of the medium. The amount of bending or refraction which occurs can be calculated using Snell’s Law (). Objective: To measure the index of refraction of Lucite
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ENZYME TIME (posted 9-7) Written by: Len Davis Creatine. Check. Arginine. Check. Protein powder. Check. Enzymes. Che . . . wait‚ what was that last one? You may not think of them as you compile your supplement shopping list‚ but enzyme products can be a smart choice for packing on muscle mass. Traditionally‚ enzymes are known as a digestive aid‚ but studies have shown that they also play an important role in recovery from high-intensity training‚ making them a prime addition to a bodybuilding
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.Potential energy and kinetic is what makes the roller coaster ascends up the hill and it descends Roller coasters the change of ds down the hill. Potential and kinetic energy is what makes the roller coaster move. What some people may not realize is that the roller coaster has no engine. When you’re going down hill they use different types of wheels to keep the ride smooth. A roller coaster is not pulled by cable. The 3 types of wheels are running wheels which guides the roller coaster‚ Friction
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Learning Objectives • • • • • • • Explore Packet Tracer Real-time mode Explore the Logical Workspace Explore Packet Tracer operation Connect devices Examine a device configuration Review the standard lab setup Overview of the devices Background Throughout the course you will be using a standard lab setup created from actual PCs‚ servers‚ routers‚ and switches to learn networking concepts. This method provides widest range of features and the most realistic experience. Since equipment and time are
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Assessment of Catalase Function Lab Introduction The purpose of this lab report was to test and measure the rate of substrate destruction by an enzyme‚ we tested the destruction of hydrogen peroxide by the enzyme catalase. Hydrogen peroxide is a poisonous by product of metabolism that can damage cells if it is not removed. Catalase is an enzyme that speeds up the breakdown of hydrogen peroxide into water and oxygen gas. H2O2 + catalase → H2O + O2 A catalyst is a substance that lowers the
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Simple Experiments on the Enzyme Catalase Aim: The aim of this practical is to use three different techniques to investigate the effect of different concentrations of the enzyme catalase on the rate of breakdown of hydrogen peroxide. Background information Catalase is an enzyme which is found in all living organisms. This enzyme catalases the decomposition of hydrogen peroxide into water and oxygen. Cells continually produce a poisonous by-product of metabolising‚ called hydrogen peroxide. This
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To investigate the effect of temperature on an enzyme controlled reaction Introduction and planning For the investigation of enzymes‚ I am going to conduct an experiment to see how temperature can affect the rate of reaction of enzymes by testing it with starch. The enzyme that we are going to use is called amylase. We are going to test this enzyme with starch. By mixing amylase and starch solutions together under different temperature conditions‚ we can record the rate of reaction by taking a
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