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Questions and Answers
A chemical reaction occurs in an isolated system. Which of the following statements is true regarding the change in internal energy ($ΔE$) of the system?
A chemical reaction occurs in an isolated system. Which of the following statements is true regarding the change in internal energy ($ΔE$) of the system?
- The $ΔE$ will be negative if the reaction is endothermic.
- The $ΔE$ will be zero because no energy can enter or leave the system. (correct)
- The $ΔE$ will be positive if the reaction is exothermic.
- The $ΔE$ will depend on the amount of work done by the system.
Consider a scenario where a gas expands against a constant external pressure while absorbing heat from the surroundings. Which of the following statements accurately describes the signs of heat (q) and work (w) in this process, according to the first law of thermodynamics?
Consider a scenario where a gas expands against a constant external pressure while absorbing heat from the surroundings. Which of the following statements accurately describes the signs of heat (q) and work (w) in this process, according to the first law of thermodynamics?
- q is negative, w is positive
- q is positive, w is negative (correct)
- Both q and w are positive
- Both q and w are negative
Which of the following processes is endothermic?
Which of the following processes is endothermic?
- Dissolving ammonium nitrate in water. (correct)
- Neutralization of a strong acid with a strong base.
- Combustion of methane gas.
- Freezing of water.
For a chemical reaction at constant pressure, the change in enthalpy ($ΔH$) is equal to:
For a chemical reaction at constant pressure, the change in enthalpy ($ΔH$) is equal to:
A system releases 500 J of heat to the surroundings and does 200 J of work on the surroundings. What is the change in internal energy ($ΔE$) of the system?
A system releases 500 J of heat to the surroundings and does 200 J of work on the surroundings. What is the change in internal energy ($ΔE$) of the system?
The internal energy of a gas increases by 300 J when it is compressed, and at the same time it gives off 600 J of heat. What is the work done on or by the gas?
The internal energy of a gas increases by 300 J when it is compressed, and at the same time it gives off 600 J of heat. What is the work done on or by the gas?
Which of the following statements correctly describes the relationship between enthalpy change ($ΔH$) and internal energy change ($ΔE$) for a reaction involving gases, where there is a decrease in the number of moles of gas?
Which of the following statements correctly describes the relationship between enthalpy change ($ΔH$) and internal energy change ($ΔE$) for a reaction involving gases, where there is a decrease in the number of moles of gas?
A 2.0 mol sample of an ideal gas expands from an initial volume of 10.0 L to a final volume of 25.0 L at a constant temperature of 300 K. Calculate the work done (in Joules) by the gas if the expansion occurs against a constant external pressure of 1.0 atm. (1 L atm = 101.3 J)
A 2.0 mol sample of an ideal gas expands from an initial volume of 10.0 L to a final volume of 25.0 L at a constant temperature of 300 K. Calculate the work done (in Joules) by the gas if the expansion occurs against a constant external pressure of 1.0 atm. (1 L atm = 101.3 J)
For the reaction N2(g) + 2O2(g) → 2NO2(g), ΔH = 68 kJ. If the reaction is reversed and the amount of N2(g) is doubled, what is the new ΔH value?
For the reaction N2(g) + 2O2(g) → 2NO2(g), ΔH = 68 kJ. If the reaction is reversed and the amount of N2(g) is doubled, what is the new ΔH value?
Given the following reactions and their enthalpies:
N2 + O2 → 2NO ΔH = 180kJ
2NO + O2 → 2NO2 ΔH = -112kJ
Calculate the enthalpy change for the reaction N2 + 2O2 → 2NO2 using Hess's Law.
Given the following reactions and their enthalpies:
N2 + O2 → 2NO ΔH = 180kJ 2NO + O2 → 2NO2 ΔH = -112kJ
Calculate the enthalpy change for the reaction N2 + 2O2 → 2NO2 using Hess's Law.
Consider the following reactions:
C2H2(g) + 5/2 O2(g) → 2 CO2(g) + H2O(l) ΔH = -1299.5kJ
C(s) + O2(g) → CO2(g) ΔH = -393.5kJ
H2(g) + ½ O2(g) → H2O(l) ΔH = -285.8kJ
What manipulations are required to calculate the enthalpy for the reaction 2C(s) + H2(g) → C2H2(g)?
Consider the following reactions:
C2H2(g) + 5/2 O2(g) → 2 CO2(g) + H2O(l) ΔH = -1299.5kJ C(s) + O2(g) → CO2(g) ΔH = -393.5kJ H2(g) + ½ O2(g) → H2O(l) ΔH = -285.8kJ
What manipulations are required to calculate the enthalpy for the reaction 2C(s) + H2(g) → C2H2(g)?
Given the following reactions:
2B(s) + 3/2O2(g) → B2O3(s) ΔH = -1273kJ
B2H6(g) + 3O2(g) → B2O3(s) + 3H2O(g) ΔH = -2035kJ
H2(g) + 1/2O2 (g) → H2O(l) ΔH = -286kJ
H2O(l) → H2O(g) ΔH = 44kJ
What series of manipulations will allow you to calculate the enthalpy for the synthesis of diborane from its elements: 2B(s) + 3H2(g) → B2H6(g)?
Given the following reactions:
2B(s) + 3/2O2(g) → B2O3(s) ΔH = -1273kJ B2H6(g) + 3O2(g) → B2O3(s) + 3H2O(g) ΔH = -2035kJ H2(g) + 1/2O2 (g) → H2O(l) ΔH = -286kJ H2O(l) → H2O(g) ΔH = 44kJ
What series of manipulations will allow you to calculate the enthalpy for the synthesis of diborane from its elements: 2B(s) + 3H2(g) → B2H6(g)?
If the enthalpy change (ΔH) for a reaction is negative, what does this indicate about the reaction?
If the enthalpy change (ΔH) for a reaction is negative, what does this indicate about the reaction?
For the reaction 2O3(g) → 3O2(g), ΔH = -427kJ and for O2(g) → 2O(g), ΔH = +495kJ What is the enthalpy change for the reaction O3(g) → 3O(g)?
For the reaction 2O3(g) → 3O2(g), ΔH = -427kJ and for O2(g) → 2O(g), ΔH = +495kJ What is the enthalpy change for the reaction O3(g) → 3O(g)?
Consider the reaction: NO(g) + O3(g) → NO2(g) + O2(g) ΔH = -199kJ, and O2(g) → 2O(g) ΔH = +495kJ. Using these reactions, determine the enthalpy (ΔH) for: NO(g) + O(g) → NO2(g)
Consider the reaction: NO(g) + O3(g) → NO2(g) + O2(g) ΔH = -199kJ, and O2(g) → 2O(g) ΔH = +495kJ. Using these reactions, determine the enthalpy (ΔH) for: NO(g) + O(g) → NO2(g)
Standard state conditions are important in thermochemistry. Which of the following conditions define standard state conditions?
Standard state conditions are important in thermochemistry. Which of the following conditions define standard state conditions?
For an exothermic reaction, which statement is true regarding the enthalpy change ($ΔH$) and the heat involved?
For an exothermic reaction, which statement is true regarding the enthalpy change ($ΔH$) and the heat involved?
Consider the reaction: $N_2(g) + 3H_2(g) \rightarrow 2NH_3(g)$ with $\Delta H = -92.2 \text{ kJ}$. What is the enthalpy change for the reverse reaction: $2NH_3(g) \rightarrow N_2(g) + 3H_2(g)$?
Consider the reaction: $N_2(g) + 3H_2(g) \rightarrow 2NH_3(g)$ with $\Delta H = -92.2 \text{ kJ}$. What is the enthalpy change for the reverse reaction: $2NH_3(g) \rightarrow N_2(g) + 3H_2(g)$?
If the complete combustion of 1 mole of ethane ($C_2H_6$) releases 1560 kJ of heat at constant pressure, what is the $\Delta H$ for the combustion of 0.5 moles of ethane?
If the complete combustion of 1 mole of ethane ($C_2H_6$) releases 1560 kJ of heat at constant pressure, what is the $\Delta H$ for the combustion of 0.5 moles of ethane?
In calorimetry, what observation typically indicates an endothermic reaction within the calorimeter?
In calorimetry, what observation typically indicates an endothermic reaction within the calorimeter?
A 25.0 g piece of metal at 85.0°C is placed in 100.0 g of water at 22.0°C. The final temperature of the water and metal is 25.6°C. Given the specific heat of water is 4.184 J/g°C, which expression calculates the specific heat ($c$) of the metal?
A 25.0 g piece of metal at 85.0°C is placed in 100.0 g of water at 22.0°C. The final temperature of the water and metal is 25.6°C. Given the specific heat of water is 4.184 J/g°C, which expression calculates the specific heat ($c$) of the metal?
Using Hess's Law, given the following reactions:
$A \rightarrow B, \Delta H_1 = -50 \text{ kJ}$
$B \rightarrow C, \Delta H_2 = 20 \text{ kJ}$
What is the enthalpy change for the reaction $A \rightarrow C$?
Using Hess's Law, given the following reactions:
$A \rightarrow B, \Delta H_1 = -50 \text{ kJ}$ $B \rightarrow C, \Delta H_2 = 20 \text{ kJ}$
What is the enthalpy change for the reaction $A \rightarrow C$?
40.0 mL of 0.50 M HCl is mixed with 40.0 mL of 0.50 M NaOH in a calorimeter. The initial temperature of both solutions is 22.0°C, and the final temperature after mixing is 25.0°C. Assuming the density of the solution is 1.0 g/mL and the specific heat capacity is 4.18 J/g°C, what is the approximate enthalpy change per mole of reaction?
40.0 mL of 0.50 M HCl is mixed with 40.0 mL of 0.50 M NaOH in a calorimeter. The initial temperature of both solutions is 22.0°C, and the final temperature after mixing is 25.0°C. Assuming the density of the solution is 1.0 g/mL and the specific heat capacity is 4.18 J/g°C, what is the approximate enthalpy change per mole of reaction?
Which of the following is NOT a direct application of Hess's Law?
Which of the following is NOT a direct application of Hess's Law?
Flashcards
Energy
Energy
The capacity to do work or produce heat.
Thermochemistry
Thermochemistry
The study of energy and its transformations, especially in relation to chemical reactions involving heat.
Thermal Energy
Thermal Energy
Energy associated with the random motion of atoms and molecules.
Potential Energy
Potential Energy
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Law of Conservation of Energy
Law of Conservation of Energy
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Exothermic Process
Exothermic Process
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Endothermic Process
Endothermic Process
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Enthalpy (ΔH)
Enthalpy (ΔH)
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Enthalpy of Reaction
Enthalpy of Reaction
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Exothermic Reaction
Exothermic Reaction
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Calorimetry
Calorimetry
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Calorimeter
Calorimeter
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Specific Heat
Specific Heat
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Molar Heat Capacity
Molar Heat Capacity
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Hess's Law
Hess's Law
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Reactant Enthalpy & Exothermic Rxn
Reactant Enthalpy & Exothermic Rxn
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Degree Sign (°)
Degree Sign (°)
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Standard Enthalpy of Reaction (△H°rxn)
Standard Enthalpy of Reaction (△H°rxn)
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Standard Enthalpy of Formation (△Hf)
Standard Enthalpy of Formation (△Hf)
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Fuel Value
Fuel Value
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Bond Enthalpy
Bond Enthalpy
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Reversing a Reaction
Reversing a Reaction
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ΔH and Stoichiometry
ΔH and Stoichiometry
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Applying Hess’s Law
Applying Hess’s Law
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Standard State Conditions
Standard State Conditions
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Enthalpies of Formation
Enthalpies of Formation
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Combining ΔH Values
Combining ΔH Values
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Cancelling Species
Cancelling Species
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Study Notes
Chapter 5: Thermochemistry
- This covers the study of energy and its transformations, especially the relationship between chemical reactions and energy changes involving heat.
Section 1: The Nature of Chemical Energy
- Energy is defined as the capacity to do work or produce heat.
- Thermodynamics is the study of energy and its transformations.
- Thermochemistry is a type of thermodynamics that studies the relationships between chemical reactions and energy changes involving heat.
- Radiant energy (solar energy) and thermal energy (energy associated with random motion of molecules) are types of energy
- Potential energy represents energy available by virtue of an object's position and kinetic energy represents energy of motion
- All forms of energy can be converted from one form to another.
- The Law of Conservation of Energy states energy cannot be created or destroyed but only converted
Section 2: First Law of Thermodynamics
- Most chemical reactions absorb or produce energy, primarily in the form of heat.
- Heat is the transfer of thermal energy between two bodies at different temperatures.
- The first law of thermodynamics states that energy cannot be created or destroyed but can be converted into different forms.
- Analyzing energy changes requires defining the system, which is the specific part of the universe of interest.
- The surroundings are the rest of the universe outside the system.
- Systems can be open, closed, or isolated.
- An exothermic process releases heat and transfers thermal energy to the surroundings
- An endothermic process requires heat to be applied to the system.
Section 3: Enthalpy
- Internal energy of a system is the sum of kinetic and potential energies of its components.
- "ΔE = q + w" represents the change in a system's internal energy where "q" is heat and "w" is work
- "#" and a + or - sign indicate the direction of energy flow
- ΔΕ is negative if exothermic because energy leaves and work is done on the surroundings; positive if endothermic because energy enters and work is done on the system.
- Enthalpy (H) helps measure the flow of heat for a system
- ΔH represents change in enthalpy as in ΔH = H(products) - H(reactants)
- If products have more enthalpy, heat will be absorbed (ΔH is positive, and the reaction is endothermic);
- If reactants have more enthalpy, heat is released (ΔH is negative, and the reaction is exothermic).
Section 4: Enthalpies of Reaction
- The enthalpy change accompanying a reaction is called the enthalpy of reaction or the heat of reaction
- The reaction 2H2(g) + O2(g) → 2H2O(g) has a △H of -483.6kJ
- A negative enthalpy change indicates the reaction is exothermic
- Enthalpy is an extensive property, contingent on the state of reactants and products.
- Enthalpy change for a reaction equals the magnitude but is opposite in sign to the reverse reaction.
Section 5: Calorimetry
- Calorimetry is the science of measuring heat by observing temperature changes when a system absorbs or discharges energy as heat.
- A calorimeter is an instrument used experimentally to measure heat change.
- Specific heat of a substance is the amount of heat required to raise the temperature of one gram of the substance by 1 degree C; units are J/g°C.
- Molar heat capacity measures heat capacity of one mole of a substance.
- Calorimeters often have two cups nested inside each other
- The inner cup holds the solution where rxn occurs
- Temperatures are measured initially and after the reaction starts
- If the solution heats up, heat is released by the reaction (exothermic); if it cools down, heat is absorbed by the reaction (endothermic).
Section 6: Hess's Law
- During reaction, if temperature rises to 31.9C from 25C, then the enthalpy can he calculated using ΔH
- During calorimetry problems, the enthalpy of the solution is calculated using "q = (mass)(specific heat)(ΔTemperature)"
- According to Hess's Law; for a given set of reactants to a particular set of products, the change in enthalpy is the same whether the reaction takes place in one step or in a series of steps.
- If a reactions is reversed, the sign of AH is reversed and AH is directly proportional to the reactants.
- If the coefficients in a balance equation are multipled by an integer, the ΔΗ is also multiplied by the same integer.
Section 7: Enthalpies of Formation
- At standard states, substances are at 1 atm and often 298K (rather than 273K as in STP).
- A degree sign (°) indicates a standard state.
- Charts provide ΔH° values for elements and compounds for calculating the standard enthalpy of reaction (ΔH°rxn).
- Hess's Law can be used to calculate standard enthalpy of reaction. Additionally, reactions also provide standard enthalpy of reaction
Section 8: Bond Enthalpies
- Energy changes from chemical reactions which involve heat are closely linked to changes in the formation and breaking of chemical bonds.
- Bond enthalpy represents the enthalpy change for breaking a particular bond in one mole of a gaseous substance.
Section 9: Foods and Fuels
- Chemical reactions that produce heat are combustion reactions
- The amount of energy released when one gram of any substance is combusted is the fuel value, which fuel values can be measured with calorimeters.
- The bodies energy comes from carbohydrates and fat, then broken down for muscles, temp control, and tissue repair
- Any unused excess is stored as fat.
- Fossil fuels like natural gas, petroleum, and coal are commonly used as fuels due to their bonds breaking and releasing heat, often for electricity.
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Description
Explore thermochemistry, the study of energy and its transformations in relation to chemical reactions. Learn about the nature of chemical energy, including potential and kinetic energy. Understand the First Law of Thermodynamics and the Law of Conservation of Energy.