Chapter 7 Energy and Chemistry

7.1 Energy

EnergyThe ability to do work. is the ability to do work. Think about it: when you have a lot of energy, you can do a lot of work; but if you’re low on energy, you don’t want to do much work. Work (w) itself is defined as a force (F) operating over a distance (Δx):

In SI, force has units of newtons (N), while distance has units of meters. Therefore, work has units of N·m. This compound unit is redefined as a jouleThe SI unit of energy. (J):

Because energy is the ability to do work, energy is also measured in joules. This is the primary unit of energy we will use here.

How much is 1 J? It is enough to warm up about one-fourth of a gram of water by 1°C. It takes about 12,000 J to warm a cup of coffee from room temperature to 50°C. So a joule is not a lot of energy. It will not be uncommon to measure energies in thousands of joules, so the kilojoule (kJ) is a common unit of energy, with 1 kJ equal to 1,000 J.

An older—but still common—unit of energy is the calorie. The calorie (cal) was originally defined in terms of warming up a given quantity of water. The modern definition of calorie equates it to joules:

One area where the calorie is used is in nutrition. Energy contents of foods are often expressed in calories. However, the calorie unit used for foods is actually the kilocalorie (kcal). Most foods indicate this by spelling the word with a capital C—Calorie. Figure 7.1 "Calories on Food Labels" shows one example. So be careful counting calories when you eat!

Figure 7.1 Calories on Food Labels

This label expresses the energy content of the food, but in Calories (which are actually kilocalories).

© Thinkstock

In the study of energy, we use the term systemThe part of the universe under study. to describe the part of the universe under study: a beaker, a flask, or a container whose contents are being observed and measured. An isolated systemA system that does not allow a transfer of energy or matter into or out of the system. is a system that does not allow a transfer of energy or matter into or out of the system. A good approximation of an isolated system is a closed, insulated thermos-type bottle. The fact that the thermos-type bottle is closed keeps matter from moving in or out, and the fact that it is insulated keeps energy from moving in or out.

One of the fundamental ideas about the total energy of an isolated system is that is does not increase or decrease. When this happens to a quantity, we say that the quantity is conserved. The statement that the total energy of an isolated system does not change is called the law of conservation of energyThe total energy of an isolated system does not increase or decrease.. As a scientific law, this concept occupies the highest level of understanding we have about the natural universe.

7.2 Work and Heat

We have already defined work as a force acting through a distance. It turns out that there are other equivalent definitions of work that are also important in chemistry.

When a certain volume of a gas expands, it works against an external pressure to expand (Figure 7.2 "Volume versus Pressure"). That is, the gas must perform work. Assuming that the external pressure P_ext is constant, the amount of work done by the gas is given by the equation

where ΔV is the change in volume of the gas. This term is always the final volume minus the initial volume,

and can be positive or negative, depending on whether V_final is larger (is expanding) or smaller (is contracting) than V_initial. The negative sign in the equation for work is important and implies that as volume expands (ΔV is positive), the gas in the system is losing energy as work. On the other hand, if the gas is contracting, ΔV is negative, and the two negative signs make the work positive, so energy is being added to the system.

Figure 7.2 Volume versus Pressure

When a gas expands against an external pressure, the gas does work.

Finally, let us consider units. Volume changes are usually expressed in units like liters, while pressures are usually expressed in atmospheres. When we use the equation to determine work, the unit for work comes out as liter·atmospheres, or L·atm. This is not a very common unit for work. However, there is a conversion factor between L·atm and the common unit of work, joules:

Using this conversion factor and the previous equation for work, we can calculate the work performed when a gas expands or contracts.

Heat is another aspect of energy. HeatThe transfer of energy from one body to another due to a difference in temperature. is the transfer of energy from one body to another due to a difference in temperature. For example, when we touch something with our hands, we interpret that object as either hot or cold depending on how energy is transferred: If energy is transferred into your hands, the object feels hot. If energy is transferred from your hands to the object, your hands feel cold. Because heat is a measure of energy transfer, heat is also measured in joules.

For a given object, the amount of heat (q) involved is proportional to two things: the mass of the object (m) and the temperature change (ΔT) evoked by the energy transfer. We can write this mathematically as

where ∝ means “is proportional to.” To make a proportionality an equality, we include a proportionality constant. In this case, the proportionality constant is labeled c and is called the specific heat capacityThe proportionality constant between heat, mass, and temperature change; also called specific heat., or, more succinctly, specific heat:

where the mass, specific heat, and change in temperature are multiplied together. Specific heat is a measure of how much energy is needed to change the temperature of a substance; the larger the specific heat, the more energy is needed to change the temperature. The units for specific heat are $\frac{\text{J}}{\text{g}\cdot \text{°C}}$ or $\frac{\text{J}}{\text{g}\cdot \text{K}}$, depending on what the unit of ΔT is. You may note a departure from the insistence that temperature be expressed in Kelvin. That is because a change in temperature has the same value whether the temperatures are expressed in degrees Celsius or kelvins.

As with any equation, when you know all but one variable in the expression for q, you can determine the remaining variable by using algebra.

Table 7.1 "Specific Heats of Various Substances" lists the specific heats of some substances. Specific heat is a physical property of substances, so it is a characteristic of the substance. The general idea is that the lower the specific heat, the less energy is required to change the temperature of the substance by a certain amount.

7.3 Enthalpy and Chemical Reactions

Now that we have shown how energy, work, and heat are related, we are ready to consider energy changes in chemical reactions. A fundamental concept is that every chemical reaction occurs with a concurrent change in energy. Now we need to learn how to properly express these energy changes.

Our study of gases in Chapter 6 "Gases" and our definition of work in Section 7.2 "Work and Heat" indicate that conditions like pressure, volume, and temperature affect the energy content of a system. What we need is a definition of energy that holds when some of these conditions are specified (somewhat similar to our definition of standard temperature and pressure in our study of gases). We define the enthalpy changeThe heat of a process at constant pressure; denoted $\Delta H$. (ΔH) as the heat of a process when pressure is held constant:

The letter H stands for “enthalpy,” a kind of energy, while the Δ implies a change in the quantity. We will always be interested in the change in H, rather than the absolute value of H itself.

When a chemical reaction occurs, there is a characteristic change in enthalpy. The enthalpy change for a reaction is typically written after a balanced chemical equation and on the same line. For example, when two moles of hydrogen react with one mole of oxygen to make two moles of water, the characteristic enthalpy change is 570 kJ. We write the equation as

A chemical equation that includes an enthalpy change is called a thermochemical equationA chemical equation that includes an enthalpy change.. A thermochemical equation is assumed to refer to the equation in molar quantities, which means it must be interpreted in terms of moles, not individual molecules.

You may have noticed that the ΔH for a chemical reaction may be positive or negative. The number is assumed to be positive if it has no sign; a + sign can be added explicitly to avoid confusion. A chemical reaction that has a positive ΔH is said to be endothermicA chemical reaction that has a positive change in enthalpy., while a chemical reaction that has a negative ΔH is said to be exothermicA chemical reaction that has a negative change in enthalpy..

What does it mean if the ΔH of a process is positive? It means that the system in which the chemical reaction is occurring is gaining energy. If one considers the energy of a system as being represented as a height on a vertical energy plot, the enthalpy change that accompanies the reaction can be diagrammed as in part (a) in Figure 7.3 "Reaction Energy": the energy of the reactants has some energy, and the system increases its energy as it goes to products. The products are higher on the vertical scale than the reactants. Endothermic, then, implies that the system gains, or absorbs, energy.

An opposite situation exists for an exothermic process, as shown in part (b) in Figure 7.3 "Reaction Energy". If the enthalpy change of a reaction is negative, the system is losing energy, so the products have less energy than the reactants, and the products are lower on the vertical energy scale than the reactants are. Exothermic, then, implies that the system loses, or gives off, energy.

Figure 7.3 Reaction Energy

(a) In an endothermic reaction, the energy of the system increases (i.e., moves higher on the vertical scale of energy). (b) In an exothermic reaction, the energy of the system decreases (i.e., moves lower on the vertical scale of energy).

How are ΔH values measured experimentally? Actually, ΔH is not measured; q is measured. But the measurements are performed under conditions of constant pressure, so ΔH is equal to the q measured.

Experimentally, q is measured by taking advantage of the equation

We premeasure the mass of the chemicals in a system. Then we let the chemical reaction occur and measure the change in temperature (ΔT) of the system. If we know the specific heat of the materials in the system (typically, we do), we can calculate q. That value of q is numerically equal to the ΔH of the process, which we can scale up to a molar scale. The container in which the system resides is typically insulated, so any energy change goes into changing the temperature of the system, rather than being leaked from the system. The container is referred to as a calorimeterA container used to measure the heat of a chemical reaction., and the process of measuring changes in enthalpy is called calorimetryThe process of measuring enthalpy changes for chemical reactions..

Figure 7.4 Calorimeters

A simple calorimeter can be constructed from some nested foam coffee cups, a cover, a thermometer, and a stirrer.

For example, suppose 4.0 g of NaOH, or 0.10 mol of NaOH, are dissolved to make 100.0 mL of aqueous solution, while 3.65 g of HCl, or 0.10 mol of HCl, are dissolved to make another 100.0 mL of aqueous solution. The two solutions are mixed in an insulated calorimeter, a thermometer is inserted, and the calorimeter is covered (see Figure 7.4 "Calorimeters" for an example setup). The thermometer measures the temperature change as the following chemical reaction occurs:

An observer notes that the temperature increases from 22.4°C to 29.1°C. Assuming that the heat capacities and densities of the solutions are the same as those of pure water, we now have the information we need to determine the enthalpy change of the chemical reaction. The total amount of solution is 200.0 mL, and with a density of 1.00 g/mL, we thus have 200.0 g of solution. Using the equation for q, we substitute for our experimental measurements and the specific heat of water (Table 7.1 "Specific Heats of Various Substances"):

Solving for q, we get

The heat q is equal to the ΔH for the reaction because the chemical reaction occurs at constant pressure. However, the reaction is giving off this amount of energy, so the actual sign on ΔH is negative:

Thus, we have the following thermochemical equation for the chemical reaction that occurred in the calorimeter:

The 1/10 coefficients are present to remind us that we started with one-tenth of a mole of each reactant, so we make one-tenth of a mole of each product. Typically, however, we report thermochemical equations in terms of moles, not one-tenth of a mole. To scale up to molar quantities, we must multiply the coefficients by 10. However, when we do this, we get 10 times as much energy. Thus, we have

The ΔH can be converted into kJ units, so our final thermochemical equation is

We have just taken our experimental data from calorimetry and determined the enthalpy change of a chemical reaction. Similar measurements on other chemical reactions can determine the ΔH values of any chemical reaction you want to study.

7.4 Stoichiometry Calculations Using Enthalpy

In Chapter 5 "Stoichiometry and the Mole", we related quantities of one substance to another in a chemical equation by performing calculations that used the balanced chemical equation; the balanced chemical equation provided equivalences that we used to construct conversion factors. For example, in the balanced chemical equation

we recognized the equivalences

where ⇔ is the mathematical symbol for “is equivalent to.” In our thermochemical equation, however, we have another quantity—energy change:

This new quantity allows us to add another equivalence to our list:

That is, we can now add an energy amount to the equivalences—the enthalpy change of a balanced chemical reaction. This equivalence can also be used to construct conversion factors so that we can relate enthalpy change to amounts of substances reacted or produced.

Note that these equivalences address a concern. When an amount of energy is listed for a balanced chemical reaction, what amount(s) of reactants or products does it refer to? The answer is that relates to the number of moles of the substance as indicated by its coefficient in the balanced chemical reaction. Thus, 2 mol of H₂ are related to −570 kJ, while 1 mol of O₂ is related to −570 kJ. This is why the unit on the energy change is kJ, not kJ/mol.

For example, consider the thermochemical equation

The equivalences for this thermochemical equation are

Suppose we asked how much energy is given off when 8.22 mol of H₂ react. We would construct a conversion factor between the number of moles of H₂ and the energy given off, −184.6 kJ:

The negative sign means that this much energy is given off.

Like any stoichiometric quantity, we can start with energy and determine an amount, rather than the other way around.

Chemistry Is Everywhere: Welding with Chemical Reactions

One very energetic reaction is called the thermite reaction. Its classic reactants are aluminum metal and iron(III) oxide; the reaction produces iron metal and aluminum oxide:

2Al(s) + Fe₂O₃(s) → Al₂O₃(s) + 2Fe(s) ΔH = −850.2 kJ

When properly done, the reaction gives off so much energy that the iron product comes off as a liquid. (Iron normally melts at 1,536°C.) If carefully directed, the liquid iron can fill spaces between two or more metal parts and, after it quickly cools, can weld the metal parts together.

Thermite reactions are used for this purpose even today. For civilian purposes, they are used to reweld broken locomotive axles that cannot be easily removed for repair. They are used to weld railroad tracks together. Thermite reactions can also be used to separate thin pieces of metal if, for whatever reason, a torch doesn’t work.

A small clay pot contains a thermite mixture. It is reacting at high temperature in the photo and will eventually produce molten metal to join the railroad tracks below it.

Source: Photo courtesy of Skatebiker, http://commons.wikimedia.org/wiki/File:Velp-thermitewelding-1.jpg.

Thermite reactions are also used for military purposes. Thermite mixtures are frequently used with additional components as incendiary devices—devices that start fires. Thermite reactions are also useful in disabling enemy weapons: a piece of artillery doesn’t work so well when it has a hole melted into its barrel because of a thermite reaction!

7.5 Hess’s Law

Now that we understand that chemical reactions occur with a simultaneous change in energy, we can apply the concept more broadly. To start, remember that some chemical reactions are rather difficult to perform. For example, consider the combustion of carbon to make carbon monoxide:

In reality, this is extremely difficult to do; given the opportunity, carbon will react to make another compound, carbon dioxide:

Is there a way around this? Yes. It comes from the understanding that chemical equations can be treated like algebraic equations, with the arrow acting like the equals sign. Like algebraic equations, chemical equations can be combined, and if the same substance appears on both sides of the arrow, it can be canceled out (much like a spectator ion in ionic equations). For example, consider these two reactions:

If we added these two equations by combining all the reactants together and all the products together, we would get

We note that 2CO₂(g) appears on both sides of the arrow, so they cancel:

We also note that there are 2 mol of O₂ on the reactant side, and 1 mol of O₂ on the product side. We can cancel 1 mol of O₂ from both sides:

What do we have left?

This is the reaction we are looking for! So by algebraically combining chemical equations, we can generate new chemical equations that may not be feasible to perform.

What about the enthalpy changes? Hess’s lawWhen chemical equations are combined algebraically, their enthalpies can be combined in exactly the same way. states that when chemical equations are combined algebraically, their enthalpies can be combined in exactly the same way. Two corollaries immediately present themselves:

1. If a chemical reaction is reversed, the sign on ΔH is changed.
2. If a multiple of a chemical reaction is taken, the same multiple of the ΔH is taken as well.

What are the equations being combined? The first chemical equation is the combustion of C, which produces CO₂:

This reaction is two times the reaction to make CO₂ from C(s) and O₂(g), whose enthalpy change is known:

According to the first corollary, the first reaction has an energy change of two times −393.5 kJ, or −787.0 kJ:

The second reaction in the combination is related to the combustion of CO(g):

The second reaction in our combination is the reverse of the combustion of CO. When we reverse the reaction, we change the sign on the ΔH:

Now that we have identified the enthalpy changes of the two component chemical equations, we can combine the ΔH values and add them:

Hess’s law is very powerful. It allows us to combine equations to generate new chemical reactions whose enthalpy changes can be calculated, rather than directly measured.

Example 10

Determine the enthalpy change of

C₂H₄ + 3O₂ → 2CO₂ + 2H₂O ΔH = ?

from these reactions:

C₂H₂ + H₂ → C₂H₄ ΔH = −174.5 kJ 2C₂H₂ + 5O₂ → 4CO₂ + 2H₂O ΔH = −1,692.2 kJ 2CO₂ + H₂ → 2O₂ + C₂H₂ ΔH = −167.5 kJ

Solution

We will start by writing chemical reactions that put the correct number of moles of the correct substance on the proper side. For example, our desired reaction has C₂H₄ as a reactant, and only one reaction from our data has C₂H₄. However, it has C₂H₄ as a product. To make it a reactant, we need to reverse the reaction, changing the sign on the ΔH:

C₂H₄ → C₂H₂ + H₂ ΔH = +174.5 kJ

We need CO₂ and H₂O as products. The second reaction has them on the proper side, so let us include one of these reactions (with the hope that the coefficients will work out when all our reactions are added):

2C₂H₂ + 5O₂ → 4CO₂ + 2H₂O ΔH = −1,692.2 kJ

We note that we now have 4 mol of CO₂ as products; we need to get rid of 2 mol of CO₂. The last reaction has 2CO₂ as a reactant. Let us use it as written:

2CO₂ + H₂ → 2O₂ + C₂H₂ ΔH = −167.5 kJ

We combine these three reactions, modified as stated:

 

What cancels? 2C₂H₂, H₂, 2O₂, and 2CO₂. What is left is

C₂H₄ + 3O₂ → 2CO₂ + 2H₂O

which is the reaction we are looking for. The ΔH of this reaction is the sum of the three ΔH values:

ΔH = +174.5 − 1,692.2 − 167.5 = −1,685.2 kJ

Test Yourself

Given the thermochemical equations

Pb + Cl₂ → PbCl₂ ΔH = −223 kJ PbCl₂ + Cl₂ → PbCl₄ ΔH = −87 kJ

determine ΔH for

2PbCl₂ → Pb + PbCl₄

Answer

+136 kJ

7.6 Formation Reactions

Hess’s law allows us to construct new chemical reactions and predict what their enthalpies of reaction will be. This is a very useful tool because now we don’t have to measure the enthalpy changes of every possible reaction. We need measure only the enthalpy changes of certain benchmark reactions and then use these reactions to algebraically construct any possible reaction and combine the enthalpies of the benchmark reactions accordingly.

But what are the benchmark reactions? We need to have some agreed-on sets of reactions that provide the central data for any thermochemical equation.

Formation reactionsA chemical reaction that forms one mole of a substance from its constituent elements in their standard states. are chemical reactions that form one mole of a substance from its constituent elements in their standard states. By standard states we mean as a diatomic molecule if that is how the element exists and the proper phase at normal temperatures (typically room temperature). The product is one mole of substance, which may require that coefficients on the reactant side be fractional (a change from our normal insistence that all coefficients be whole numbers). For example, the formation reaction for methane (CH₄) is

The formation reaction for carbon dioxide (CO₂) is

In both cases, one of the elements is a diatomic molecule because that is the standard state for that particular element. The formation reaction for H₂O—

—is not in a standard state because the coefficient on the product is 2; for a proper formation reaction, only one mole of product is formed. Thus, we have to divide all coefficients by 2:

On a molecular scale, we are using half of an oxygen molecule, which may be problematic to visualize. However, on a molar level, it implies that we are reacting only half of a mole of oxygen molecules, which should be an easy concept for us to understand.

Given the formula of any substance, you should be able to write the proper formation reaction for that substance.

The enthalpy change for a formation reaction is called the enthalpy of formationThe enthalpy change for a formation reaction; denoted ΔHf. and is given the symbol ΔH_f. The subscript f is the clue that the reaction of interest is a formation reaction. Thus, for the formation of FeO(s),

Note that now we are using kJ/mol as the unit because it is understood that the enthalpy change is for one mole of substance. Note, too, by definition, that the enthalpy of formation of an element is exactly zero because making an element from an element is no change. For example,

Formation reactions and their enthalpies are important because these are the thermochemical data that are tabulated for any chemical reaction. Table 7.2 "Enthalpies of Formation for Various Substances" lists some enthalpies of formation for a variety of substances; in some cases, however, phases can be important (e.g., for H₂O).

It is easy to show that any general chemical equation can be written in terms of the formation reactions of its reactants and products, some of them reversed (which means the sign must change in accordance with Hess’s law). For example, consider

We can write it in terms of the (reverse) formation reaction of NO₂ and the formation reaction of N₂O₄:

We must multiply the first reaction by 2 to get the correct overall balanced equation. We are simply using Hess’s law in combining the ΔH_f values of the formation reactions.

Now that we have established formation reactions as the major type of thermochemical reaction we will be interested in, do we always need to write all the formation reactions when we want to determine the enthalpy change of any random chemical reaction? No. There is an easier way. You may have noticed in all our examples that we change the signs on all the enthalpies of formation of the reactants, and we don’t change the signs on the enthalpies of formation of the products. We also multiply the enthalpies of formation of any substance by its coefficient—technically, even when it is just 1. This allows us to make the following statement: the enthalpy change of any chemical reaction is equal to the sum of the enthalpies of formation of the products minus the sum of the enthalpies of formation of the reactants. In mathematical terms,

where n_p and n_r are the number of moles of products and reactants, respectively (even if they are just 1 mol), and ΔH_f,p and ΔH_f,r are the enthalpies of formation of the product and reactant species, respectively. This products-minus-reactants scheme is very useful in determining the enthalpy change of any chemical reaction, if the enthalpy of formation data are available. Because the mol units cancel when multiplying the amount by the enthalpy of formation, the enthalpy change of the chemical reaction has units of energy (joules or kilojoules) only.