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Calculate the enthalpy change for the reaction $$ \mathrm{P}_{4} \mathrm{O}_{6}(s)+2 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) $$ given the following enthalpies of reaction: $$ \begin{array}{ll} \mathrm{P}_{4}(s)+3 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{6}(s) & \Delta H=-1640.1 \mathrm{~kJ} \\ \mathrm{P}_{4}(s)+5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) & \Delta H=-2940.1 \mathrm{~kJ} \end{array} $$

Short Answer

Expert verified
The enthalpy change for the reaction \(\mathrm{P}_{4} \mathrm{O}_{6}(s)+2 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s)\) can be calculated using Hess's Law and the given enthalpy changes for the two other reactions. After reversing the first given reaction and adding it to the second given reaction to obtain the target reaction, the enthalpy change for the target reaction is found to be \(\Delta H_{target} = -1300 \mathrm{~kJ}\).

Step by step solution

01

Write down the target reaction

First, let's write down the reaction we want to find the enthalpy change for: \( \mathrm{P}_{4} \mathrm{O}_{6}(s)+2 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) \)
02

Analyze the given reactions and adjust them to match the target reaction

We have the following two given reactions: 1) \( \mathrm{P}_{4}(s)+3 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{6}(s) \quad \Delta H=-1640.1 \mathrm{~kJ} \) 2) \( \mathrm{P}_{4}(s)+5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) \quad \Delta H=-2940.1 \mathrm{~kJ} \) Looking at the target reaction, we can see that P4O6 is a reactant, but in the first given reaction, it is a product. So, we'll reverse reaction 1: Reversed Reaction 1) \( \mathrm{P}_{4} \mathrm{O}_{6}(s) \longrightarrow \mathrm{P}_{4}(s)+3 \mathrm{O}_{2}(g) \quad \Delta H=1640.1 \mathrm{~kJ} \) Now let's add the reversed reaction 1 with reaction 2: Reversed Reaction 1 + Reaction 2) \( \mathrm{P}_{4} \mathrm{O}_{6}(s) + \mathrm{P}_{4}(s)+5 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4}(s)+3 \mathrm{O}_{2}(g) + \mathrm{P}_{4} \mathrm{O}_{10}(s) \) We can cancel out the P4(s) from both sides of the equation, and we will be left with the target reaction: Target Reaction) \( \mathrm{P}_{4} \mathrm{O}_{6}(s)+2 \mathrm{O}_{2}(g) \longrightarrow \mathrm{P}_{4} \mathrm{O}_{10}(s) \)
03

Add up the adjusted enthalpy changes to find the enthalpy change for the target reaction

Since we reversed the first reaction and added it to the second reaction to obtain the target reaction, we have to add their enthalpy changes according to Hess's Law: \( \Delta H_{target} = 1640.1 \mathrm{~kJ} - 2940.1 \mathrm{~kJ} \) Now, let's calculate the enthalpy change for the target reaction: \( \Delta H_{target} = -1300 \mathrm{~kJ} \) The enthalpy change for the target reaction is -1300 kJ.

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Most popular questions from this chapter

Under constant-volume conditions, the heat of combustion of benzoic acid \(\left(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\right)\) is \(26.38 \mathrm{~kJ} / \mathrm{g}\). A 2.760 -g sample of benzoic acid is burned in a bomb calorimeter. The temperature of the calorimeter increases from \(21.60^{\circ} \mathrm{C}\) to \(29.93^{\circ} \mathrm{C}\). (a) What is the total heat capacity of the calorimeter? (b) \(\mathrm{A}\) 1.440-g sample of a new organic substance is combusted in the same calorimeter. The temperature of the calorimeter increases from \(22.14^{\circ} \mathrm{C}\) to \(27.09^{\circ} \mathrm{C}\). What is the heat of combustion per gram of the new substance? (c) Suppose that in changing samples, a portion of the water in the calorimeter were lost. In what way, if any, would this change the heat capacity of the calorimeter?

(a) When a \(0.235-\mathrm{g}\) sample of benzoic acid is combusted in a bomb calorimeter (Figure 5.19 ), the temperature rises \(1.642{ }^{\circ} \mathrm{C}\). When a 0.265 -g sample of caffeine, \(\mathrm{C}_{8} \mathrm{H}_{10} \mathrm{O}_{2} \mathrm{~N}_{4}\), is burned, the temperature rises \(1.525^{\circ} \mathrm{C}\). Using the value \(26.38 \mathrm{~kJ} / \mathrm{g}\) for the heat of combustion of benzoic acid, calculate the heat of combustion per mole of caffeine at constant volume. (b) Assuming that there is an uncertainty of \(0.002^{\circ} \mathrm{C}\) in each temperature reading and that the masses of samples are measured to 0.001 \(\mathrm{g}\), what is the estimated uncertainty in the value calculated for the heat of combustion per mole of caffeine?

(a) Why is the change in enthalpy usually easier to measure than the change in internal energy? (b) \(H\) is a state function, but \(q\) is not a state function. Explain. (c) For a given process at constant pressure, \(\Delta H\) is positive. Is the process endothermic or exothermic?

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 \((177 \mathrm{~mL}) ?\)

You are given \(\Delta H\) for a process that occurs at constant pressure. What additional information do you need to determine \(\Delta E\) for the process?

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