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From the enthalpies of reaction $$\begin{aligned} 2 \mathrm{C}(s)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}(g) & \Delta H=-221.0 \mathrm{kJ} \\ 2 \mathrm{C}(s)+\mathrm{O}_{2}(g)+4 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{CH}_{3} \mathrm{OH}(g) & \Delta H=-402.4 \mathrm{kJ} \end{aligned}$$ calculate \(\Delta H\) for the reaction $$\mathrm{CO}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{CH}_{3} \mathrm{OH}(g)$$

Short Answer

Expert verified
Therefore, the enthalpy change for the target reaction is: \(\Delta H = \Delta H_2 - \Delta H'_1 = -402.4 kJ - 110.5 kJ = -512.9 kJ\)

Step by step solution

01

Define the target reaction

Our target reaction is: \(CO(g) + 2 H_{2}(g) \longrightarrow CH_{3}OH(g)\)
02

Analyze the given reactions

We are given two reactions: Reaction 1: \(2 C(s) + O_{2}(g) \longrightarrow 2 CO(g) \qquad \Delta H_1 = -221.0 kJ\) Reaction 2: \(2 C(s) + O_{2}(g) + 4 H_{2}(g) \longrightarrow 2 CH_{3}OH(g) \qquad \Delta H_2 = -402.4 kJ\)
03

Modify the given reactions to obtain the target reaction

To obtain the target reaction from the given reactions, we can perform the following operations: 1. Divide Reaction 1 by 2. 2. Reverse the modified Reaction 1. 3. Subtract the modified Reaction 1 from Reaction 2. Reaction 1 (modified): \(\frac{1}{2}(2 C(s) + O_{2}(g) \longrightarrow 2 CO(g))\) \(C(s) + \frac{1}{2}O_{2}(g) \longrightarrow CO(g) \qquad \frac{\Delta H_1}{2} = -110.5 kJ\) Reverse Reaction 1 (modified): \(CO(g) \longrightarrow C(s) + \frac{1}{2}O_{2}(g) \qquad \Delta H'_1 = 110.5 kJ\) Finally, \(Reaction\, 2 - Reverse\, Reaction\, 1 (modified)\) \(2 C(s) + O_{2}(g) + 4 H_{2}(g) - [CO(g) - (C(s) + \frac{1}{2}O_{2}(g))] \longrightarrow 2 CH_{3}OH(g) - C(s) - \frac{1}{2}O_{2}(g)\) \(CO(g) + 2 H_{2}(g) \longrightarrow CH_{3}OH(g)\)

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Key Concepts

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

Thermochemistry
Thermochemistry is the study of energy changes that occur during chemical reactions and changes in state. In many reactions, energy is either absorbed or released, and this energy change is often linked to the concept of enthalpy, denoted as \(\Delta H\).

Enthalpy is the heat content of a system at constant pressure. When a reaction releases heat, it is exothermic and \(\Delta H\) is negative. Conversely, when a reaction absorbs heat, it is endothermic and \(\Delta H\) is positive.

In our example, comparing the given reactions reveals their heat changes. The calculated \(\Delta H\) values are critical in determining whether the reactions are exothermic or endothermic, providing insight into the energy flow during the reactions. Changes in enthalpy help predict whether reactions will occur naturally.
  • Reactions that release heat (negative \(\Delta H\)) are often more spontaneous.
  • The values of enthalpy changes are key for applications in various fields like environmental science and engineering.
Hess's Law
Hess's Law is a crucial principle in thermochemistry, stating that the total enthalpy change for a chemical reaction is the same, irrespective of the pathway the reaction takes. This is incredibly useful because it allows us to calculate enthalpy changes that might not be easily measurable directly.

In the original problem, to find \(\Delta H\) for the target reaction \(CO(g) + 2 H_{2}(g) \longrightarrow CH_{3}OH(g)\), we applied Hess's Law by manipulating the given reactions. By reversing and scaling reactions, we reshaped them to derive the desired reaction while adjusting \(\Delta H\).

This exemplifies how Hess's Law simplifies complex calculations, enabling us to effectively determine the energy changes for reactions without directly measuring them.
  • Hess's Law underlines the concept of conservation of energy.
  • It is invaluable for complex reactions encountered in industrial and laboratory settings.
Chemical Reactions
Chemical reactions involve the transformation of reactants into products through the breaking and formation of chemical bonds. They vary widely, from simple combinations to complex decomposition or substitutions.

The reactions given in the problem demonstrate how elements like carbon, oxygen, and hydrogen can form different compounds through chemical processes. Understanding the enthalpy changes helps illustrate how energy is distributed in these transformations.

In the exercise, the manipulation of equations shows the complex interplay of such reactions, underscoring the dependency on parameters like temperature and pressure.
  • Reactant bonds are broken, requiring energy, and new products are formed, releasing energy.
  • Chemical equilibrium plays a key role in determining the direction and extent of reactions.
These concepts connect to broader themes in chemistry, such as reaction rates and catalysis, and are foundational for understanding diverse scientific phenomena and industrial processes.

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Most popular questions from this chapter

In a thermodynamic study, a scientist focuses on the properties of a solution in an apparatus as illustrated. A solution is continuously flowing into the apparatus at the top and out at the bottom, such that the amount of solution in the apparatus is constant with time. (a) Is the solution in the apparatus a closed system, open system, or isolated system? (b) If the inlet and outlet were closed, what type of system would it be?

Using values from Appendix \(\mathrm{C}\) , calculate the standard enthalpy change for each of the following reactions: $$ \begin{array}{l}{\text { (a) } 2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g)} \\ {\text { (b) } \mathrm{Mg}(\mathrm{OH})_{2}(s) \longrightarrow \mathrm{MgO}(s)+\mathrm{H}_{2} \mathrm{O}(l)} \\ {\text { (c) } \mathrm{N}_{2} \mathrm{O}_{4}(g)+4 \mathrm{H}_{2}(g) \longrightarrow \mathrm{N}_{2}(g)+4 \mathrm{H}_{2} \mathrm{O}(g)} \\ {\text { (d) } \mathrm{SiCl}_{4}(l)+2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{SiO}_{2}(s)+4 \mathrm{HCl}(g)}\end{array} $$

Ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) is 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 ky of heat emitted.

Consider the combustion of liquid methanol, \(\mathrm{CH}_{3} \mathrm{OH}(l) :\) $$\begin{aligned} \mathrm{CH}_{3} \mathrm{OH}(l)+\frac{3}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(l) & \\ \Delta H &=-726.5 \mathrm{kJ} \end{aligned}$$ (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.

Calculate \(\Delta E\) and determine whether the process is endothermic or exothermic for the following cases: (a) \(q=0.763 \mathrm{kJ}\) and \(w=-840 \mathrm{J} .\) (b) A system releases 66.1 \(\mathrm{kJ}\) of heat to its surroundings while the surroundings do 44.0 \(\mathrm{kJ}\) of work on the system.

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