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Limestone stalactites and stalagmites are formed in caves by the following reaction: $$ \mathrm{Ca}^{2+}(a q)+2 \mathrm{HCO}_{3}^{-}(a q) \longrightarrow \mathrm{CaCO}_{3}(s)+\mathrm{CO}_{2}(g)+\mathrm{H}_{2} \mathrm{O}(l) $$ If \(1 \mathrm{~mol}\) of \(\mathrm{CaCO}_{3}\) forms at \(298 \mathrm{~K}\) under 1 atm pressure, the reaction performs \(2.47 \mathrm{~kJ}\) of \(P-V\) work, pushing back the atmosphere as the gaseous \(\mathrm{CO}_{2}\) forms. At the same time, \(38.95 \mathrm{~kJ}\) of heat is absorbed from the environment. What are the values of \(\Delta H\) and of \(\Delta E\) for this reaction?

Short Answer

Expert verified
For the given reaction, the internal energy change (∆E) is \(41.42 \: \text{kJ/mol}\) and the enthalpy change (∆H) is \(43.89 \: \text{kJ/mol}\).

Step by step solution

01

Recall the first law of thermodynamics formula

The first law of thermodynamics states: \[ ∆E = q + w \] where ∆E is the change in internal energy, q is the heat, and w is the work done by (or on) the system.
02

Calculate the internal energy change from the heat and work values

Given the heat (q) = 38.95 kJ and P-V work (w) = 2.47 kJ, we can find ∆E as follows: \[ ∆E = q + w = 38.95 + 2.47 = 41.42 \: \text{kJ/mol}\]
03

Recall the relationship between enthalpy change, internal energy change, and P-V work

The relationship between enthalpy change (∆H), internal energy change (∆E), and P-V work (w) is given by: \[ ∆H = ∆E + w \]
04

Calculate the enthalpy change using the relationships derived in Step 3

Using the calculated internal energy change (∆E = 41.42 kJ/mol) and the given P-V work (w = 2.47 kJ/mol), we can find the enthalpy change as follows: \[ ∆H = ∆E + w = 41.42 + 2.47 = 43.89 \: \text{kJ/mol}\]
05

Present the final answer for the enthalpy change and internal energy change in the reaction

For the given reaction, we have calculated the values of the internal energy change and the enthalpy change as follows: - The internal energy change (∆E) = 41.42 kJ/mol - The enthalpy change (∆H) = 43.89 kJ/mol

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Most popular questions from this chapter

(a) State the first law of thermodynamics. (b) What is meant by the internal energy of a system? (c) By what means can the internal energy of a closed system increase?

(a) What are the units of molar heat capacity? (b) What are the units of specific heat? (c) If you know the specific heat of copper, what additional information do you need to calculate the heat capacity of a particular piece of copper pipe?

The heat of combustion of ethanol, \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)\), is \(-1367 \mathrm{~kJ} / \mathrm{mol}\). A batch of Sauvignon Blanc wine contains \(10.6 \%\) ethanol by mass. Assuming the density of the wine to be \(1.0 \mathrm{~g} / \mathrm{mL}\), what is the caloric content due to the alcohol (ethanol) in a 6-oz glass of wine \((177 \mathrm{~mL})\) ?

Suppose that the gas-phase reaction \(2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow\) \(2 \mathrm{NO}_{2}(g)\) were carried out in a constant-volume container at constant temperature. (a) Would the measured heat change represent \(\Delta H\) or \(\Delta E\) ? (b) If there is a difference, which quantity is larger for this reaction? (c) Explain your answer to part (b).

Consider the combustion of liquid methanol, \(\mathrm{CH}_{3} \mathrm{OH}(l)\) : $$ \begin{array}{r} \mathrm{CH}_{3} \mathrm{OH}(l)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l) \\ \Delta H=-726.5 \mathrm{~kJ} \end{array} $$ (a) What is the enthalpy change for the reverse reaction? (b) Balance the forward reaction with whole-number coefficients. What is \(\Delta H\) for the reaction represented by this equation? (c) Which is more likely to be thermodynamically favored, the forward reaction or the reverse reaction? (d) If the reaction were written to produce \(\mathrm{H}_{2} \mathrm{O}(g)\) instead of \(\mathrm{H}_{2} \mathrm{O}(l)\), would you expect the magnitude of \(\Delta H\) to increase, decrease, or stay the same? Explain.

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