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(a) Why is the change in enthalpy usually easier to measure than the change in internal energy? (b) \(H\) is a state function, but \(q\) is not a state function. Explain. (c) For a given process at constant pressure, \(\Delta H\) is positive. Is the process endothermic or exothermic?

Short Answer

Expert verified
(a) The change in enthalpy (\(\Delta H\)) is easier to measure than the change in internal energy (\(\Delta U\)) because most experiments occur at constant pressure, making \(\Delta H\) equal to the heat absorbed or released. Measuring work, which is required to calculate \(\Delta U\), is difficult in practice. (b) Enthalpy (\(H\)) is a state function as it depends only on the system's current state (being the sum of \(U, P,\) and \(V\), all state functions). Heat (\(q\)) is not a state function as it depends on the path taken. (c) A process with a positive change in enthalpy (\(\Delta H > 0\)) at constant pressure is endothermic, as it involves absorption of heat by the system.

Step by step solution

01

(a) Comparison between measuring change in enthalpy and change in internal energy

Enthalpy (\(H\)) is a thermodynamic property defined as the sum of the system's internal energy (\(U\)) and the product of its pressure (\(P\)) and volume (\(V\)): \(H = U + PV\). The change in enthalpy (\(\Delta H\)) is usually easier to measure than the change in internal energy (\(\Delta U\)) because most practical experiments and reactions occur at constant pressure. Under constant pressure conditions, the change in enthalpy (\(\Delta H\)) is equal to the heat absorbed or released by the system (\(q_p\)): \(\Delta H = q_p\). However, the change in internal energy (\(\Delta U\)) involves measuring the changes in both heat (\(q\)) and work (\(w\)) done by or on the system, since \(\Delta U = q + w\). Measuring work is quite difficult in practice, especially for chemical reactions, while measuring heat absorbed or released is relatively easier. Therefore, it is more convenient to measure the change in enthalpy than the change in internal energy.
02

(b) Enthalpy as a state function and heat not being a state function

State functions are properties that depend only on the current state of the system and are independent of the path taken to reach that state. Enthalpy (\(H\)) is a state function because it is defined as the sum of the system's internal energy (\(U\), also a state function) and the product of pressure (\(P\), a state function) and volume (\(V\), a state function): \(H = U + PV\). On the other hand, heat (\(q\)) is not a state function because it is a form of energy transfer that depends on the path taken. The amount of heat transferred between two states of a system is not solely determined by the initial and final states but depends on the process through which the system changes.
03

(c) Determining whether a process is endothermic or exothermic based on the change in enthalpy

A process at constant pressure has a positive change in enthalpy (\(\Delta H > 0\)). Based on the definition of enthalpy and its relationship with heat at constant pressure conditions (\(\Delta H = q_p\)), a positive value for \(\Delta H\) implies that the heat has been absorbed by the system from its surroundings. Since endothermic processes involve absorption of heat by the system, a process with a positive change in enthalpy at constant pressure is endothermic.

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Most popular questions from this chapter

Ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) is currently blended with gasoline as an automobile fuel. (a) Write a balanced equation for the combustion of liquid ethanol in air. (b) Calculate the standard enthalpy change for the reaction, assuming \(\mathrm{H}_{2} \mathrm{O}(g)\) as a product. (c) Calculate the heat produced per liter of ethanol by combustion of ethanol under constant pressure. Ethanol has a density of \(0.789 \mathrm{~g} / \mathrm{mL}\). (d) Calculate the mass of \(\mathrm{CO}_{2}\) produced per \(\mathrm{kJ}\) of heat emitted.

(a) When a 4.25 -g sample of solid ammonium nitrate dissolves in \(60.0 \mathrm{~g}\) of water in a coffee-cup calorimeter (Figure 5.18), the temperature drops from \(22.0^{\circ} \mathrm{C}\) to \(16.9^{\circ} \mathrm{C}\). Calculate \(\Delta H\left(\right.\) in \(\left.\mathrm{kJ} / \mathrm{mol} \mathrm{NH}_{4} \mathrm{NO}_{3}\right)\) for the solution process $$ \mathrm{NH}_{4} \mathrm{NO}_{3}(s) \longrightarrow \mathrm{NH}_{4}^{+}(a q)+\mathrm{NO}_{3}^{-}(a q) $$ Assume that the specific heat of the solution is the same as that of pure water. (b) Is this process endothermic or exothermic?

When a \(6.50-\mathrm{g}\) sample of solid sodium hydroxide dissolves in \(100.0 \mathrm{~g}\) of water in a coffee-cup calorimeter (Figure 5.18 ), the temperature rises from \(21.6^{\circ} \mathrm{C}\) to \(37.8^{\circ} \mathrm{C}\). Calculate \(\Delta H\) (in \(\mathrm{kJ} / \mathrm{mol} \mathrm{NaOH})\) for the solution process $$ \mathrm{NaOH}(s) \longrightarrow \mathrm{Na}^{+}(a q)+\mathrm{OH}^{-}(a q) $$ Assume that the specific heat of the solution is the same as that of pure water.

Three common hydrocarbons that contain four carbons are listed here, along with their standard enthalpies of formation: (a) For each of these substances, calculate the molar enthalpy of combustion to \(\mathrm{CO}_{2}(g)\) and \(\mathrm{H}_{2} \mathrm{O}(l) .\) (b) Calculate the fuel value in \(\mathrm{kJ} / \mathrm{g}\) for each of these compounds. \((\mathrm{c})\) For each hydrocarbon, determine the percentage of hydrogen by mass. (d) By comparing your answers for parts (b) and (c), propose a relationship between hydrogen content and fuel value in hydrocarbons.

Given the data $$ \begin{aligned} \mathrm{N}_{2}(g)+\mathrm{O}_{2}(g) & \longrightarrow 2 \mathrm{NO}(g) & & \Delta H=+180.7 \mathrm{~kJ} \\ 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) & \longrightarrow 2 \mathrm{NO}_{2}(g) & & \Delta H=-113.1 \mathrm{~kJ} \\ 2 \mathrm{~N}_{2} \mathrm{O}(g) & \longrightarrow 2 \mathrm{~N}_{2}(g)+\mathrm{O}_{2}(g) & \Delta H &=-163.2 \mathrm{~kJ} \end{aligned} $$ use Hess's law to calculate \(\Delta H\) for the reaction $$ \mathrm{N}_{2} \mathrm{O}(g)+\mathrm{NO}_{2}(g) \longrightarrow 3 \mathrm{NO}(g) $$

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