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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Most popular questions from this chapter

(a) Under what condition will the enthalpy change of a process equal the amount of heat transferred into or out of the system? (b) During a constant- pressure process, the system releases heat to the surroundings. Does the enthalpy of the system increase or decrease during the process? (c) In a constant-pressure process, \(\Delta H=0 .\) What can you conclude about \(\Delta E, q,\) and \(w ?\)

At one time, a common means of forming small quantities of oxygen gas in the laboratory was to heat \(\mathrm{KClO}_{3} :\) $$2 \mathrm{KClO}_{3}(s) \longrightarrow 2 \mathrm{KCl}(s)+3 \mathrm{O}_{2}(g) \quad \Delta H=-89.4 \mathrm{kJ}$$ For this reaction, calculate \(\Delta H\) for the formation of (a) 1.36 \(\mathrm{mol}\) of \(\mathrm{O}_{2}\) and \((\mathbf{b}) 10.4 \mathrm{g}\) of \(\mathrm{KCl}\) (c) The decomposition of \(\mathrm{KClO}_{3}\) proceeds spontaneously when it is heated. Do you think that the reverse reaction, the formation of \(\mathrm{KClO}_{3}\) from \(\mathrm{KCl}\) and \(\mathrm{O}_{2},\) is likely to be feasible under ordinary conditions? Explain your answer.

Can you use an approach similar to Hess's law to calculate the change in internal energy, \(\Delta E,\) for an overall reaction by summing the \(\Delta E\) values of individual reactions that add up to give the desired overall reaction?

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?

How much work (in J) is involved in a chemical reaction if the volume decreases from 5.00 to 1.26 L against a constant pressure of 0.857 atm?

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