A system goes from state 1 to state 2 and back to state 1 . (a) What is the relationship between the value of \(\Delta E\) for going from state 1 to state 2 to that for going from state 2 back to state \(1 ?\) (b) Without further information, can you conclude anything about the amount of heat transferred to the system as it goes from state 1 to state 2 as compared to that upon going from state 2 back to state \(1 ?(\mathrm{c})\) Suppose the changes in state are reversible processes. Can you conclude anything about the work done by the system upon going from state 1 to state 2 as compared to that upon going from state 2 back to state \(1 ?\)

Short Answer

Expert verified
(a) The relationship between the energy changes is: \(\Delta E_{1 \to 2} = -\Delta E_{2 \to 1}\). (b) We cannot conclude anything about the heat transfers without further information, as heat transfer depends on the specific path taken by a system during the process. (c) If the processes are reversible, the work done during the two processes is equal in magnitude but opposite in sign: \(W_{1 \to 2} = -W_{2 \to 1}\).

Step by step solution

01

Identify the relationship between the energy changes between the two processes

The energy change of a system is given by the equation: \[\Delta E = E_{final} - E_{initial}\] For going from state 1 to state 2: \[\Delta E_{1 \to 2} = E_2 - E_1\] For going back from state 2 to state 1: \[\Delta E_{2 \to 1} = E_1 - E_2\] By analyzing these two equations, we can determine the relationship between the energy changes.
02

Determine the relationship

By comparing the two equations: \[\Delta E_{1 \to 2} = -(E_1 - E_2)\] \[\Delta E_{2 \to 1} = E_1 - E_2\] We can see that: \[\Delta E_{1 \to 2} = -\Delta E_{2 \to 1}\] #Part (b): Heat Transfer Comparison#
03

Determine if we can conclude anything about heat transfer

It is not possible to determine anything about the heat transfer for these processes without further information. Heat transfer depends on the specific path taken by a system during the process, not only on its initial and final states. #Part (c): Work Done Comparison (Assuming Reversible Processes)#
04

Determine if we can conclude anything about the work done

In case the changes in state are reversible processes, we can use the fact that \(\Delta E\) depends on the heat, \(Q\), and the work, \(W\). Specifically, \[\Delta E = Q - W\] Since we already found the relationship between the energy changes in part (a), we can rewrite the equation in terms of heat and work: \[Q_{1 \to 2} - W_{1 \to 2} = - (Q_{2 \to 1} - W_{2 \to 1})\] If the processes are reversible, the heat transfers will be the same for both processes but with opposite signs (because reversible processes are path-independent regarding heat transfer). Thus, \[Q_{1 \to 2} = -Q_{2 \to 1}\] Using this information, we can conclude that the work done during the two processes is equal in magnitude but opposite in sign: \[W_{1 \to 2} = -W_{2 \to 1}\]

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Most popular questions from this chapter

The \(K_{b}\) for methylamine \(\left(\mathrm{CH}_{3} \mathrm{NH}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix D. (a) Write the chemical equation for the equilibrium that corresponds to \(K_{b} .\) (b) By using the value of \(K_{b},\) calculate \(\Delta G^{\circ}\) for the equilibrium in part (a). (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=6.7 \times 10^{-9} \mathrm{M},\left[\mathrm{CH}_{3} \mathrm{NH}_{3}^{+}\right]=2.4 \times 10^{-3} \mathrm{M}\) and \(\left[\mathrm{CH}_{3} \mathrm{NH}_{2}\right]=0.098 \mathrm{M} ?\)

(a) What do you expect for the sign of \(\Delta S\) in a chemical reaction in which two moles of gaseous reactants are converted to three moles of gaseous products? (b) For which of the processes in Exercise 19.11 does the entropy of the system increase?

Indicate whether \(\Delta G\) increases, decreases, or does not change when the partial pressure of \(\mathrm{H}_{2}\) is increased in each of the following reactions: (a) \(\mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g)\) (b) \(2 \mathrm{HBr}(g) \longrightarrow \mathrm{H}_{2}(g)+\mathrm{Br}_{2}(g)\) (c) \(2 \mathrm{H}_{2}(g)+\mathrm{C}_{2} \mathrm{H}_{2}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{6}(g)\)

For each of the following pairs, choose the substance with the higher entropy per mole at a given temperature: (a) \(\operatorname{Ar}(l)\) or \(\mathrm{Ar}(g),\) (b) \(\mathrm{He}(g)\) at 3 atm pressure or \(\mathrm{He}(g)\) at 1.5 atm pressure, (c) \(1 \mathrm{~mol}\) of \(\mathrm{Ne}(g)\) in \(15.0 \mathrm{~L}\) or \(1 \mathrm{~mol}\) of \(\mathrm{Ne}(g)\) in \(1.50 \mathrm{~L}\), (d) \(\mathrm{CO}_{2}(g)\) or \(\mathrm{CO}_{2}(s)\).

In each of the following pairs, which compound would you expect to have the higher standard molar entropy: (a) \(\mathrm{C}_{2} \mathrm{H}_{2}(g)\) or \(\mathrm{C}_{2} \mathrm{H}_{6}(g)\) (b) \(\mathrm{CO}_{2}(g)\) or \(\mathrm{CO}(g) ?\) Explain.

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