/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 100 How many grams of methane \(\lef... [FREE SOLUTION] | 91Ó°ÊÓ

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How many grams of methane \(\left[\mathrm{CH}_{4}(g)\right]\) must be combusted to heat \(1.00 \mathrm{~kg}\) of water from \(25.0^{\circ} \mathrm{C}\) to \(90.0^{\circ} \mathrm{C}\), assuming \(\mathrm{H}_{2} \mathrm{O}(l)\) as a product and \(100 \%\) efficiency in heat transfer?

Short Answer

Expert verified
\(q = 1000 \times 4.18 \times 65 = 271700 \, \mathrm{J}\) #tag_title#Step 2: Determine the amount of methane needed to produce the required heat#tag_content#The combustion of methane can be represented by the balanced chemical equation: \(\mathrm{CH}_{4}(g) + 2\mathrm{O}_{2}(g) \rightarrow \mathrm{CO}_{2}(g) + 2\mathrm{H}_{2}\mathrm{O}(l)\) The heat of combustion of methane is -890.8 kJ/mol, meaning that 890.8 kJ of heat is released when 1 mol of methane is combusted. First, we need to convert the heat required to kilojoules: \(271700 \, \mathrm{J} = 271.7 \, \mathrm{kJ}\) Now we can determine the amount of methane needed by setting up a proportion: \(\frac{890.8 \, \mathrm{kJ}}{1 \, \mathrm{mol} \, \mathrm{CH}_{4}} = \frac{271.7 \, \mathrm{kJ}}{x \, \mathrm{mol} \, \mathrm{CH}_{4}}\) Solving for x, we get: \(x = \frac{271.7 \, \mathrm{kJ} \times 1 \, \mathrm{mol} \, \mathrm{CH}_{4}}{890.8 \, \mathrm{kJ}} = 0.305 \, \mathrm{mol} \, \mathrm{CH}_{4}\) Finally, we convert the moles of methane to grams by using the molar mass of methane (16.04 g/mol): \(0.305 \, \mathrm{mol} \, \mathrm{CH}_{4} \times \frac{16.04 \, \mathrm{g}}{1 \, \mathrm{mol} \, \mathrm{CH}_{4}} = 4.89 \, \mathrm{g} \, \mathrm{CH}_{4}\) So, 4.89 grams of methane must be combusted to heat 1.00 kg of water from 25.0 °C to 90.0 °C, assuming 100 % efficiency in heat transfer.

Step by step solution

01

Calculate the heat required to heat the water

First, we need to determine the amount of heat (q) required to heat the 1.00 kg of water from 25.0 °C to 90.0 °C. We use the formula: q = mcΔT, where m is the mass of water, c is the specific heat capacity of water, and ΔT is the change in temperature. The specific heat capacity of water (c) is 4.18 J/g°C, the mass (m) is 1000 g (since 1 kg = 1000 g), and the change in temperature (ΔT) is (90.0 - 25.0) °C. Now, we can calculate the heat required: q = (1000 g) × (4.18 J/g°C) × (90.0 - 25.0) °C

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Most popular questions from this chapter

Given the data $$ \begin{aligned} \mathrm{N}_{2}(g)+\mathrm{O}_{2}(g)-\cdots+2 \mathrm{NO}(g) & \Delta H=+180.7 \mathrm{~kJ} \\ 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \cdots-\rightarrow 2 \mathrm{NO}_{2}(g) & \Delta H=-113.1 \mathrm{~kJ} \\ 2 \mathrm{~N}_{2} \mathrm{O}(g)-\cdots 2 \mathrm{~N}_{2}(g)+\mathrm{O}_{2}(g) & \Delta H=-163.2 \mathrm{~kJ} \end{aligned} $$ use Hess's law to calculate \(\Delta H\) for the reaction $$ \mathrm{N}_{2} \mathrm{O}(g)+\mathrm{NO}_{2}(g) \stackrel{-\cdots} 3 \mathrm{NO}(g) $$

Consider the twodiagramsbelow. (a) Based on \((t)\), write an equation showing how \(\Delta H_{\mathrm{A}}\) is related to \(\Delta H_{\mathrm{B}}\) and \(\Delta H_{\mathrm{C}}\). How do both diagram (i) and your equation relate to the fact that enthalpy is a state function? (b) Based on (ii), write an equation relating \(\Delta H_{Z}\) to the other enthalpy changes in the diagram. (c) How do these diagrams relate to Hess's law? [Section 5.6]

(a) When a 0.235-g sample of benzoic acid is combusted in a bomb calorimeter, 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) What is meant by the term state function? (b) Give an example of a quantity that is a state function and one that is not. (c) Is work a state function? Why or why not?

The air bags that provide protection in autos in the event of an accident expand because of a rapid chemical reaction. From the viewpoint of the chemical reactants as the system, what do you expect for the signs of \(q\) and \(w\) in this process?

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