A handbook lists two different values for the heat of combustion of hydrogen: \(33.88 \mathrm{kcal} / \mathrm{g} \mathrm{H}_{2}\) if \(\mathrm{H}_{2} \mathrm{O}(\mathrm{l})\) is formed, and \(28.67 \mathrm{kcal} / \mathrm{g} \mathrm{H}_{2}\) if \(\mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) is formed. Explain why these two values are different, and indicate what property this difference represents. Devise a means of verifying your conclusions.

Short Answer

Expert verified
The values for heat of combustion of hydrogen differ based on whether liquid water or water vapor is formed due to the energy involved in the phase change, represented by the heat (enthalpy) of vaporization. Verification of this conclusion can be performed by conducting a controlled combustion of hydrogen and measuring the heat released when each state of water is formed.

Step by step solution

01

Understanding the Problem and Concepts

The heat of combustion refers to the amount of heat released during a combustion reaction. In this scenario, hydrogen is the substance combusting and forming water. The difference in heat of combustion when water is formed as a liquid versus when it is formed as a gas can be primarily attributed to the heat of vaporization: the energy required to change water from a liquid to a gas (or, conversely, the energy released when changing from gas to liquid).
02

Identify the Property

The property representing this difference is known as enthalpy (Heat) of vaporization (ΔHvap), which is the energy required for the phase change from a liquid to vapor, and this energy is additional to the enthalpy of formation since more energy is required to form water vapor rather than liquid water.
03

Devise a Verification Method

To validate this conclusion, an experiment may be performed where hydrogen is combusted under controlled conditions to form both water liquid (under one set of conditions) and water vapor (under another set of conditions). By carefully measuring the heat released in each case, the difference in values related to the heat of combustion based on the state of water formed can be observed, confirming that the difference corresponds to the heat of vaporization.

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Most popular questions from this chapter

What is the change in internal energy of a system if the surroundings (a) transfer 235 J of heat and 128 J of work to the system; (b) absorb 145 J of heat from the system while doing \(98 \mathrm{J}\) of work on the system; (c) exchange no heat, but receive 1.07 kJ of work from the system?

How much heat, in kilojoules, is evolved in the complete combustion of (a) \(1.325 \mathrm{g} \mathrm{C}_{4} \mathrm{H}_{10}(\mathrm{g})\) at \(25^{\circ} \mathrm{C}\) and \(1 \mathrm{atm} ;\) (b) \(28.4 \mathrm{L} \mathrm{C}_{4} \mathrm{H}_{10}(\mathrm{g})\) at \(\mathrm{STP} ;(\mathrm{c})\) \(12.6 \mathrm{LC}_{4} \mathrm{H}_{10}(\mathrm{g})\) at \(23.6^{\circ} \mathrm{C}\) and \(738 \mathrm{mmHg} ?\) Assume that the enthalpy change for the reaction does not change significantly with temperature or pressure. The complete combustion of butane, \(\mathrm{C}_{4} \mathrm{H}_{10}(\mathrm{g}),\) is represented by the equation $$\begin{array}{r} \mathrm{C}_{4} \mathrm{H}_{10}(\mathrm{g})+\frac{13}{2} \mathrm{O}_{2}(\mathrm{g}) \longrightarrow 4 \mathrm{CO}_{2}(\mathrm{g})+5 \mathrm{H}_{2} \mathrm{O}(1) \\ \Delta H^{\circ}=-2877 \mathrm{kJ} \end{array}$$

James Joule published his definitive work related to the first law of thermodynamics in \(1850 .\) He stated that "the quantity of heat capable of increasing the temperature of one pound of water by \(1^{\circ} \mathrm{F}\) requires for its evolution the expenditure of a mechanical force represented by the fall of 772 lb through the space of one foot." Validate this statement by relating it to information given in this text.

The heat of solution of \(\mathrm{NaOH}(\mathrm{s})\) in water is \(-41.6 \mathrm{kJ} / \mathrm{mol} \mathrm{NaOH} .\) When \(\mathrm{NaOH}(\mathrm{s})\) is dissolved in water the solution temperature (a) increases; (b) decreases; (c) remains constant; (d) either increases or decreases, depending on how much NaOH is dissolved.

Use Hess's law and the following data $$\begin{aligned} \mathrm{CH}_{4}(\mathrm{g})+2 \mathrm{O}_{2}(\mathrm{g}) \longrightarrow \mathrm{CO}_{2}(\mathrm{g})+2 \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \\ \Delta H^{\circ}=-802 \mathrm{kJ} \end{aligned}$$ $$\begin{aligned} \mathrm{CH}_{4}(\mathrm{g})+\mathrm{CO}_{2}(\mathrm{g}) \longrightarrow 2 \mathrm{CO}(\mathrm{g})+2 \mathrm{H}_{2}(\mathrm{g}) & \\ \Delta H^{\circ}=&+247 \mathrm{kJ} \end{aligned}$$ $$\begin{aligned} \mathrm{CH}_{4}(\mathrm{g})+\mathrm{CO}_{2}(\mathrm{g}) \longrightarrow 2 \mathrm{CO}(\mathrm{g})+2 \mathrm{H}_{2}(\mathrm{g}) & \\ \Delta H^{\circ}=&+247 \mathrm{kJ} \end{aligned}$$ $$\begin{aligned} \mathrm{CH}_{4}(\mathrm{g})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow \mathrm{CO}(\mathrm{g})+3 \mathrm{H}_{2}(\mathrm{g}) & \\ \Delta H^{\circ}=&+206 \mathrm{kJ} \end{aligned}$$ to determine \(\Delta H^{\circ}\) for the following reaction, an important source of hydrogen gas $$\mathrm{CH}_{4}(\mathrm{g})+\frac{1}{2} \mathrm{O}_{2}(\mathrm{g}) \longrightarrow \mathrm{CO}(\mathrm{g})+2 \mathrm{H}_{2}(\mathrm{g})$$

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