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(a) Under what condition will the enthalpy change of a process equal the amount of heat transferred into or out of the system? (b) During a constant- pressure process, the system releases heat to the surroundings. Does the enthalpy of the system increase or decrease during the process? (c) In a constant-pressure process, \(\Delta H=0 .\) What can you conclude about \(\Delta E, q,\) and \(w ?\)

Short Answer

Expert verified
(a) The enthalpy change, \(\Delta H\), equals the amount of heat transferred, \(q\), at constant pressure (\(\Delta H = q_P\)). (b) In a constant-pressure process with heat release, the enthalpy decreases, as both \(q\) and \(\Delta H\) are negative. (c) When \(\Delta H = 0\) in a constant-pressure process, the heat exchanged (\(q\)) is equal to the difference between the work done by the gas on its surroundings (\(w\)) and the pressure-volume work done (\(P\Delta V\)).

Step by step solution

01

(a) Condition when enthalpy change equals heat transferred

The enthalpy change of a process, \(\Delta H\), is equal to the amount of heat transferred into or out of the system (\(q\)), under the condition of constant pressure. Mathematically, this can be written as: \[ \Delta H = q_P, \] where \(q_P\) is the heat transferred at constant pressure.
02

(b) Enthalpy change during a constant-pressure process with heat release

During a constant-pressure process, the system releases heat to the surroundings. This means that the heat transfer is negative (\(q < 0\)). According to the equation stated earlier, \(\Delta H = q_P\), the enthalpy change will also be negative (\((ΔH < 0)\)) during the process. Therefore, the enthalpy of the system decreases during the process.
03

(c) Analysing the relationship between \(\Delta H\), \(\Delta E\), \(q\), and \(w\) when \(\Delta H=0\)

In a constant-pressure process, the enthalpy change is related to the internal energy change, heat, and work as follows: \[ \Delta H = \Delta E + P\Delta V, \] where \(\Delta E\) is the change in internal energy, \(P\) is the constant pressure, and \(\Delta V\) is the change in volume. When \(\Delta H = 0\), the equation becomes: \[ 0 = \Delta E + P\Delta V. \] Considering the first law of thermodynamics, which relates internal energy change, heat, and work, we have: \[ \Delta E = q - w, \] where \(w\) is the work done by the gas on its surroundings. By substituting this expression for \(\Delta E\) into the equation for constant pressure, we obtain: \[ 0 = (q - w) + P\Delta V. \] Solving for \(q\), we find: \[ q = w - P\Delta V. \] This indicates that when the enthalpy change is 0 during a constant-pressure process, the heat exchanged between the system and its surroundings (\(q\)) is equal to the difference between the work done by the gas on its surroundings (\(w\)) and the pressure-volume work done (\(P\Delta V\)).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

constant pressure
Constant pressure is a condition in thermodynamics where the pressure of a system does not change during a process. This situation is particularly useful when analyzing chemical reactions and physical changes because it simplifies the calculations involved. At constant pressure, the relationship between enthalpy change (\(\Delta H\)) and heat transfer is straightforward:
  • Enthalpy change equals the heat transferred to or from the system.
  • This relationship is expressed mathematically by the equation \(\Delta H = q_P\), where \(q_P\) is the heat transferred at constant pressure.

During a constant-pressure process, if the system releases heat to its surroundings, the heat transfer is negative (\(q < 0\)). This means the system's enthalpy decreases, as indicated by a negative enthalpy change (\(\Delta H < 0\)). It's a simple yet powerful concept often encountered in thermodynamic studies.
heat transfer
Heat transfer involves the movement of thermal energy from one object or system to another. This can occur in several ways, such as conduction, convection, and radiation. In the context of thermodynamics and constant pressure, understanding heat transfer is crucial.
  • At constant pressure, the entire heat transfer during a process is equated to the change in enthalpy (\(\Delta H\)).
  • When heat is released by the system, the value of \(q\) is negative, indicating energy flow out of the system.
  • Conversely, when heat is absorbed, \(q\) is positive, and the system gains energy.

Heat transfer is a core concept in understanding how energy transactions affect the state and phase of a system. It is essential for analyzing processes in chemistry and engineering.
first law of thermodynamics
The first law of thermodynamics is a fundamental principle stating that energy cannot be created or destroyed, only transferred or transformed. Mathematically, it is expressed as:\[\Delta E = q - w,\]where \(\Delta E\) is the change in internal energy, \(q\) is the heat transferred to the system, and \(w\) is the work done by the system.
In constant-pressure processes, this law interconnects with enthalpy changes:
  • When \(\Delta H = 0\), energy balance becomes apparent: the heat added equals the work done minus any pressure-volume work.
  • Substituting \(\Delta E = q - w\) into the enthalpy equation \(\Delta H = \Delta E + P\Delta V\), we find \(q = w - P\Delta V\).
  • This showcases the intricate balance between heat, work, and internal energy in constant-pressure scenarios.

Understanding this law is crucial for grasping how energy conservation applies in real-world thermodynamic systems, ensuring energy changes are accurately accounted for across processes.

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Most popular questions from this chapter

Diethyl ether, \(\mathrm{C}_{4} \mathrm{H}_{10} \mathrm{O}(l),\) a flammable compound that was once used as a surgical anesthetic, has the structure $$\mathrm{H}_{3} \mathrm{C}-\mathrm{CH}_{2}-\mathrm{O}-\mathrm{CH}_{2}-\mathrm{CH}_{3}$$ The complete combustion of 1 mol of \(\mathrm{C}_{4} \mathrm{H}_{10} \mathrm{O}(l)\) to \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(l)\) yields \(\Delta H^{\circ}=-2723.7 \mathrm{kJ}\) . (a) Write a balanced equation for the combustion of 1 \(\mathrm{mol}\) of \(\mathrm{C}_{4} \mathrm{H}_{10} \mathrm{O}(l) .\) (b) By using the information in this problem and data in Table \(5.3,\) calculate \(\Delta H_{f}^{\circ}\) for diethyl ether.

Under constant-volume conditions, the heat of combustion of glucose \(\left(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}\right)\) is 15.57 \(\mathrm{kJ} / \mathrm{g}\) . A 3.500 -g sample of glucose is burned in a bomb calorimeter. The temperature of the calorimeter increases from 20.94 to \(24.72^{\circ} \mathrm{C}\) (a) What is the total heat capacity of the calorimeter? (b) If the size of the glucose sample had been exactly twice as large, what would the temperature change of the calorimeter have been?

Consider the following reaction: $$2 \mathrm{CH}_{3} \mathrm{OH}(g) \longrightarrow 2 \mathrm{CH}_{4}(g)+\mathrm{O}_{2}(g) \quad \Delta H=+252.8 \mathrm{kJ}$$ (a) Is this reaction exothermic or endothermic? (b) Calculate the amount of heat transferred when 24.0 of \(\mathrm{CH}_{3} \mathrm{OH}(g)\) is decomposed by this reaction at constant pressure. (c) For a given sample of \(\mathrm{CH}_{3} \mathrm{OH},\) the enthalpy change during the reaction is 82.1 kJ. How many grams of methane gas are produced? (\mathbf{d} ) How many kilojoules of heatare released when 38.5 \(\mathrm{g}\) of \(\mathrm{CH}_{4}(g)\) reacts completely with \(\mathrm{O}_{2}(g)\) to form \(\mathrm{CH}_{3} \mathrm{OH}(g)\) at constant pressure?

Can you use an approach similar to Hess's law to calculate the change in internal energy, \(\Delta E,\) for an overall reaction by summing the \(\Delta E\) values of individual reactions that add up to give the desired overall reaction?

A coffee-cup calorimeter of the type shown in Figure 5.18 contains 150.0 g of water at \(25.1^{\circ} \mathrm{C} .\) A \(121.0-\mathrm{g}\) block of copper metal is heated to \(100.4^{\circ} \mathrm{C}\) by putting it in a beaker of boiling water. The specific heat of \(\mathrm{Cu}(s)\) is \(0.385 \mathrm{J} / \mathrm{g}-\mathrm{K}\) . The Cu is added to the calorimeter, and after a time the contents of the cup reach a constant temperature of \(30.1^{\circ} \mathrm{C}\) (a) Determine the amount of heat, in J, lost by the copper block. (b) Determine the amount of heat gained by the water. The specific heat of water is \(4.18 \mathrm{J} / \mathrm{g}-\mathrm{K}\) . (c) The difference between your answers for (a) and (b) is due to heat loss through the Styrofoam cups and the heat necessary to raise the temperature of the inner wall of the apparatus. The heat capacity of the calorimeter is the amount of heat necessary to raise the temperature of the apparatus (the cups and the stopper) by 1 K. Calculate the heat capacity of the calorimeter in J/K. (d)What would be the final temperature of the system if all the heat lost by the copper block were absorbed by the water in the calorimeter?

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