The Enthalpy of Formation of Magnesium Carbonate

Abstract: An ice calorimeter was used to study the reaction of magnesium metal and 1.00M

Step 3: Use the thermometer to identify and record the temperature for room temperature, in your refrigerator, in your freezer, and then research the temperature of boiling water (do not take this temperature) and record them in Table 2.

In order to measure the heats of reactions, add the reactants into the calorimeter and measure the difference between the initial and final temperature. The temperature difference helps us calculate the heat released or absorbed by the reaction. The equation for calorimetry is q=mc(ΔT). ΔT is the temperature change, m is the mass, c is the specific heat capacity of the solution, and q is the heat transfer. Given that the experiment is operated under constant pressure in the lab, the temperature change is due to the enthalpy of the reaction, therefore the heat of the reaction can be calculated.

    In this lab, a calorimeter was used to find the enthalpy of reaction for two reactions, the first was between magnesium and 1 molar hydrochloric acid, and the second was between magnesium oxide and 1 molar hydrochloric acid. After the enthalpy for both of these were found, Hess’ law was used to find the molar enthalpy of combustion of magnesium, using the enthalpies for the two previous reactions and the enthalpy of formation for water. The enthalpy of reaction for the magnesium + hydrochloric acid reaction was found to be -812.76 kJ. The enthalpy of reaction for the magnesium oxide + hydrochloric acid reaction was found to be -111.06 kJ. These two enthalpies and the enthalpy of formation for water were manipulated and added together using Hess’s law to get the molar enthalpy of combustion of magnesium. It was found that the molar enthalpy of combustion of magnesium was -987.5 kJ/mol. The accepted enthalpy was -601.6 kJ/mol, which means that there is a percent difference of 64%. This percent difference is very high which indicates that this type of experiment is very inefficient for finding the molar enthalpy of combustion of magnesium. Most likely, a there are many errors in this simple calorimeter experiment that make it inefficient for finding the molar enthalpy of combustion of magnesium.

About 80 mL of HCl was obtained and mixed with phenolphthalein. Using a LabQuest unit and Gas Pressure Sensor kit, the HCl mixture was added to the flask with the magnesium ribbon and allowed to react. When reaction was complete, the change of temperature and gas was recorded. This procedure was repeated for different masses of magnesium ribbon (masses found on page 89 of the lab manual). After the completed procedure, moles of H₂ produced in each trial were calculated. (The actual procedure can be found on pages 87-89 of the lab manual)

Experiment 2 focused on finding the enthalpy of solution of magnesium chloride. Testing the enthalpy of solution started with measuring out 10 mL of deionized water in a graduated cylinder for three separate trials, each trial having a different mass of magnesium chloride. The water was then poured into a well of a Styrofoam calorimeter then the initial temperature of water was taken using a temperature probe and the LoggerPro programming. A measured amount of magnesium chloride was placed in the same well as the water in the calorimeter,

Because it is dangerous to burn magnesium, it is not possible to directly record heat change. Our lab team suggests an indirect way of determining the heat of combustion for magnesium. To accomplish this, we need to perform two separate trials. One uses a solid (powder) version of MgO, while the other uses Mg ribbon. With the results from these, we can use Hess’ Law to determine q=∆H. This provides both a safe and successful way of indirectly determining the heat of combustion for magnesium.

If 10.0g of solid baking soda is poured into 30 mL of citric acid, then a reaction will occur and an increase in temperature will be observed. Whereas, if a piece of magnesium metal is added to 30 mL of Hydrochloric Acid, then a reaction will occur and an increase in temperature will be observable. For Part 3 of the experiment, if 50 mL of tap water is placed in a can 2.5 cm inches above a burning marshmallow, then through the process of calorimetry the energy content of the marshmallow should be 5.0kJ/g (the value provided by the United States Department of Agriculture).

How empirical formula of Magnesium Oxide is obtained by heating Magnesium in the presence of air?

Purpose: To utilize a calorimeter correctly to find the enthalpy changes in two different reactions. The purpose was also to use concepts of specific heat to observe the relationship between temperature observations and heat transfer. Then, use the equations to see the relationship between change in energy and the amount of substance involved. Use Hess’ law to determine the change in energy.

The volume of carbon dioxide gas produced from a reaction was measured in order to determine what carbonate sample was used. A gas assembly apparatus was used to capture the gas from a reaction between an unknown carbonate and 6M hydrochloric acid; three trials were performed. The mass of the unknown carbonate was determined, and the reaction occurred in a test tube. The volume of gas produced by the reaction was measured, and the partial pressure of carbon dioxide was calculated after the partial pressure of water vapor was determined using Dalton’s Law of Partial Pressures. The percent mass of carbon dioxide gas was then calculated, and the average mass percent was compared to the table of known carbonates. It was concluded that the unknown carbonate sample used in the reaction was magnesium carbonate.

The theoretical molar enthalpy was calculated by using Hess’ Law of Summation. The theoretical values of the standard molar enthalpy of formation, also known as delta H not of formation, were taken from the product side of the net ionic equation and added up; the delta H not of formation values for the reactants were also added up. Following Hess’s Law of Summation, the change in enthalpy per mole of reaction, delta H not of reaction, is equal to that of the total delta H not of formation reactants subtracted from the total delta H not of formation of the products, to calculate the theoretical molar enthalpy of reaction.

LEARNING OBJECTIVES The learning objectives of this experiment are to. . . ! ! determine changes in enthalpy and entropy of the reaction of zinc with copper sulfate using two methods: electrochemistry and calorimetry. compare the enthalpy values obtained by the two methods. BACKGROUND Thermodynamics is concerned with energy changes that occur in chemical and physical process es. The enthalpy and entropy changes of a system undergoing such processes are interrelated by the change in free energy, ªG, according to the equation

Experiment to investigate factors affecting the rate of reaction between magnesium ribbon and hydrochloric acid

Introduction: Every chemical change is accompanied by a change in energy usually in the form of heat. If heat is evolved, the reaction is exothermic, and if heat is absorbed, the reaction is endothermic. The energy change of a reaction that occurs at constant pressure is called the heat of reaction or the enthalpy of reaction (ΔHr). This quantity of heat is measured experimentally by allowing the reaction to occur in a calorimeter. In this experiment you will determine the heat of neutralization when an acid and a base react to form 1 mole of water. In a perfect calorimeter, heat is exchanged only between the reaction and the calorimeters water. Technically, some heat may may be absorbed the calorimeter. All calorimeters exchange some heat with its environment. This amount of heat is called the calorimeters heat capacity (the amount of of heat required to raise its temperature 1∘Celsius). We are going to “pretend” that our calorimeter is the perfect calorimeter.