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Thermochemistry

Thermochemistry

Edited By Shivani Poonia | Updated on Jul 02, 2025 05:59 PM IST

Thermochemistry deals with heat and energies associated with different physical transformations and chemical reactions. Energy is either absorbed during an endothermic reaction, or it can be released, exothermic. The main concern of thermochemistry, however, is the change in energy, usually regarding the exchange of energy of a system with its surroundings.

Thermochemistry
Thermochemistry

The laws of thermodynamics tell us that the energy of an isolated system is constant. If it is not an isolated system, then, in any chemical reaction, the energy remains conserved. Thermochemistry helps in understanding energy change, heat change, and spontaneity of reactions. All reactions share a common factor of heat, work, and heat-work relationship. In a reaction, the work can be done on the system or the work can be done by the system. Similarly, heat can either be absorbed or heat given out of the system. A study of all these also helps in determining the actual energy available in food.

Thermochemistry

It deals with the heat changes during chemical reactions. It is called chemical energetics and is based on the first law of thermodynamics.

Exothermic Reaction

Heat is evolved here.
$\Delta \mathrm{H}$ is -ve as $\mathrm{H}_{\mathrm{R}}>\mathrm{H}_{\mathrm{P}}$
$\Delta \mathrm{H}=\mathrm{H}_{\mathrm{P}}-\mathrm{H}_{\mathrm{R}}=-$ ve (at constant pressure)
At constant volume, $\Delta \mathrm{E}=\left(\mathrm{E}_{\mathrm{P}}-\mathrm{E}_{\mathrm{R}}\right)=-\mathrm{ve}$ that is. $\mathrm{E}_{\mathrm{R}}>\mathrm{E}_{\mathrm{P}}$

Endothermic Reaction

Here heat is absorbed.
$\Delta H$ or $\Delta E=+$ ve for endothermic $\Delta H=H_p-H_R=+$ ve ( at constant pressure as ) as $H_p>H_R$ or $E_p>E_R$
At constant volume
$$
\Delta E=\left(E_p-E_R\right)=+v e
$$

Heat or Enthalpy of Reaction

It is the change in enthalpy (amount of heat evolved or absorbed) when the number of gm-moles of the substance indicated by a chemical reaction has undergone a complete reaction.

It is determined by water and Bomb calorimeters Mathematically, it is given as
$
=\Sigma \mathrm{H}_{\mathrm{p}}-\Sigma \mathrm{H}_{\mathrm{R}}
$

It can be express by $[\Delta \mathrm{H}]_{\mathrm{p}}$ or $[\Delta \mathrm{E}]_{\mathrm{v}}$ at constant pressure and volume respectively.

Some Solved Examples

Example 1: When combustion of ethylene ( C2H4) takes place it releases carbon dioxide and water. If the enthalpy of formation of C2H4 is$w$, for $\mathrm{O}_2$ is $x$, for $\mathrm{CO}_2$ is $y$ and for $\mathrm{H}_2 \mathrm{O}_{\text {is }} z$.z. Then find the enthalpy of the reaction:

1) $y+z-w-x$
2) $W+3 x-2 y-2 z$
3) $2 y+2 z-w-3 x$

4)All of the above

Solution:

Enthalpy of reaction, $\Delta H=H_P-H_R$

First, write the balanced equation of the reaction

$\mathrm{C}_2 \mathrm{H}_4+3 \mathrm{O}_2 \rightarrow 2 \mathrm{CO}_2+2 \mathrm{H}_2 \mathrm{O}$

Given:
$
\begin{aligned}
& \Delta H_f^0 C_2 H_4=w \\
& \Delta H_f^0 O_2=x \\
& \Delta H_f^0 C O_2=y \\
& \Delta H_f^0 H_2 O=z
\end{aligned}
$

Now, $\Delta H=(2 y+2 z)-(w+3 x)=2 y+2 z-w-3 x$

Example 2: When combustion of Methane (CH4 ) takes place it releases carbon dioxide and water. If the enthalpy of formation of CH4 is 10J, for O2 us OJ, for CO2 us 5J and for H2O us 3J and only 50% CH4 is converted then the enthalpy of reaction and nature of the reaction is:

1)-0.5J, Exothermic

2) +0.5J, Endothermic

3)-1J, Exothermic

4)+1J, Endothermic

Solution:

Enthalpy of reaction, $\Delta H=H_P-H_R$

First, write the balanced equation of the reaction

$\mathrm{CH}_4+2 \mathrm{O}_2 \rightarrow \mathrm{CO}_2+2 \mathrm{H}_2 \mathrm{O}$

$\begin{aligned} & \Delta H_f^0 C H_4=10 \mathrm{~J} \\ & \Delta H_f^0 O_2=0 \mathrm{~J} \\ & \Delta H_f^0 C O_2=5 \mathrm{~J} \\ & \Delta H_f^0 H_2 O=3 \mathrm{~J}\end{aligned}$

As the conversion is only 50% then all reactants and products will also be converted 50%.

So,$\Delta H=5 \times 0.5+2 \times 3 \times 0.5-0-10 \times 0.5=2.5+3-5=+0.5 \mathrm{~J}$

Hence it is an endothermic process

Example 3: If $\Delta H$ is the change in enthalpy and $\Delta E$ the change in internal energy accompanying a gaseous reaction, then

1) $\Delta H$is always greater than $\Delta E$

2)$\Delta H<\Delta E$ only if the number of moles of the products is greater than the number of the reactants

3)$\Delta H$ is always less than $\Delta H$

4) $\Delta H<\Delta E$ only if the number of moles of the products is less than the number of the reactants

Solution:

We know this formula

$\Delta \mathrm{H}=\Delta \mathrm{E}-\Delta \mathrm{ng}_{\mathrm{g}} R \mathrm{TT}$

From the above formula only possible statement -

$\Delta H<\Delta E$$\Delta H<\Delta E$ only if the number of moles of the products is less than the number of the reactants.

And rest statements are incorrect.

Example 4: For which of the following reactions, $\Delta \mathrm{E}=\Delta \mathrm{H}$ ?

$\begin{aligned} & \text { 1) } \mathrm{N}_2 \mathrm{O}_4(\mathrm{~g}) \rightleftharpoons 2 \mathrm{NO}_2(\mathrm{~g}) \\ & \text { 2) } 2 \mathrm{SO}_2(\mathrm{~g})+\mathrm{O}_2(\mathrm{~g}) \rightleftharpoons 2 \mathrm{SO}_3(\mathrm{~g}) \\ & \text { 3) } \mathrm{H}_2(\mathrm{~g})+\mathrm{I}_2(\mathrm{~g}) \rightleftharpoons 2 \mathrm{HI}(\mathrm{g}) \\ & \text { 4) } 2 \mathrm{H}_2(\mathrm{~g})+\mathrm{O}_2(\mathrm{~g}) \rightleftharpoons 2 \mathrm{H}_2 \mathrm{O}(\mathrm{l})\end{aligned}$

Solution:

$
\begin{aligned}
& \Delta H=\Delta E+(\Delta n) R T \\
& \Delta H=\Delta E \text { when } \Delta n=0
\end{aligned}
$

Out of the given reactions, $\Delta \mathrm{n}=0$ for
$
\mathrm{H}_2(\mathrm{~g})+\mathrm{I}_2(\mathrm{~g}) \rightleftharpoons 2 \mathrm{HI}(\mathrm{g})
$

Summary

In thermodynamics, the system refers to that 'part' which is under study. The 'part' of the universe excluding the system is called the surroundings. A boundary separates the system and surroundings. For example, while a student does the inorganic salt analysis, salt becomes a system while the container and the laboratory become the surroundings and walls of the container biome the boundary.Thermochemistry involves the heat energy associated with chemical reactions and physical state changes, the basic principles of which are founded upon the First Law of Thermodynamics: energy is conserved. Major terms to be noted are enthalpy, H, and enthalpy change, ΔH. Exothermic reactions are those in which heat is given off (negative ΔH), whereas in an endothermic reaction, heat is taken in (positive ΔH). Calorimetry is used for the measurement of the heat exchanged in a reaction.

Frequently Asked Questions (FAQs)

1. What is thermochemistry and how does it relate to thermodynamics?
Thermochemistry is a branch of thermodynamics that focuses on the heat energy involved in chemical reactions and physical changes. It studies the transfer of heat between a chemical system and its surroundings. Thermochemistry is essential in understanding energy changes during chemical processes, which is a fundamental aspect of thermodynamics.
2. What is the difference between exothermic and endothermic reactions?
Exothermic reactions release heat energy to the surroundings, resulting in an increase in the surrounding temperature. Endothermic reactions, on the other hand, absorb heat energy from the surroundings, causing a decrease in the surrounding temperature. The key difference lies in the direction of heat transfer between the system and its environment.
3. How does the First Law of Thermodynamics apply to chemical reactions?
The First Law of Thermodynamics, also known as the law of conservation of energy, states that energy cannot be created or destroyed, only converted from one form to another. In chemical reactions, this law ensures that the total energy of the system and surroundings remains constant. Any energy change in the system must be balanced by an equal and opposite change in the surroundings.
4. What is enthalpy and how is it measured in chemical reactions?
Enthalpy is a measure of the total heat content of a system. In chemical reactions, the change in enthalpy (ΔH) represents the heat absorbed or released at constant pressure. It is typically measured using a calorimeter, which quantifies the heat exchange between the reaction and its surroundings. Enthalpy changes are expressed in units of energy, such as joules (J) or kilojoules (kJ).
5. Why do some endothermic reactions occur spontaneously despite requiring energy input?
Some endothermic reactions occur spontaneously because of an increase in entropy (disorder) of the system. The Second Law of Thermodynamics states that the total entropy of an isolated system always increases. If the increase in entropy is large enough to overcome the unfavorable enthalpy change, the reaction can still be spontaneous. This concept is captured in the Gibbs free energy equation: ΔG = ΔH - TΔS.
6. What is Hess's Law and how is it used in thermochemistry?
Hess's Law states that the total enthalpy change in a chemical process is independent of the pathway and depends only on the initial and final states. This law allows us to calculate the enthalpy change for a reaction that is difficult to measure directly by breaking it down into a series of steps with known enthalpy changes. It's based on the principle that enthalpy is a state function.
7. How does bond breaking and bond formation contribute to the overall enthalpy change of a reaction?
Bond breaking is an endothermic process that requires energy, while bond formation is exothermic and releases energy. The overall enthalpy change of a reaction is the difference between the energy required to break bonds in the reactants and the energy released when new bonds form in the products. If more energy is released in bond formation than is required for bond breaking, the reaction is exothermic, and vice versa.
8. What is the significance of standard enthalpy of formation?
The standard enthalpy of formation (ΔHf°) is the enthalpy change when one mole of a compound is formed from its constituent elements in their standard states at 1 atm pressure and a specified temperature (usually 25°C). It's significant because it provides a reference point for calculating enthalpy changes in reactions and allows for the comparison of the stability of different compounds.
9. How does temperature affect the rate and spontaneity of chemical reactions?
Temperature affects both the rate and spontaneity of chemical reactions. Higher temperatures generally increase reaction rates by providing more kinetic energy to reactant molecules, increasing the frequency and energy of collisions. Regarding spontaneity, temperature's effect is captured in the Gibbs free energy equation (ΔG = ΔH - TΔS). As temperature increases, the TΔS term becomes more significant, potentially changing a non-spontaneous reaction to a spontaneous one if ΔS is positive.
10. What is the relationship between internal energy and enthalpy?
Internal energy (U) is the total energy contained within a system, including kinetic and potential energy of particles. Enthalpy (H) is defined as the sum of internal energy and the product of pressure and volume (H = U + PV). At constant pressure, the change in enthalpy (ΔH) is equal to the heat transferred (q) in the process. The relationship between ΔU and ΔH is given by ΔH = ΔU + PΔV.
11. How does the concept of entropy relate to thermochemistry?
Entropy is a measure of the disorder or randomness in a system. In thermochemistry, entropy changes (ΔS) play a crucial role in determining the spontaneity of reactions alongside enthalpy changes. Processes that increase disorder (like gas formation or dissolution) have positive ΔS, while those that increase order have negative ΔS. The interplay between enthalpy and entropy changes determines the overall spontaneity of a reaction, as described by the Gibbs free energy equation.
12. What is the significance of the heat capacity of a substance in thermochemistry?
Heat capacity is the amount of heat required to raise the temperature of a substance by one degree Celsius. It's significant in thermochemistry because it determines how much energy a substance can absorb or release for a given temperature change. This property is crucial in calorimetry experiments and in understanding the thermal behavior of substances in chemical reactions and physical processes.
13. How do phase changes affect the enthalpy of a system?
Phase changes involve significant enthalpy changes without temperature change. During melting, vaporization, or sublimation (endothermic processes), the system absorbs heat from the surroundings. Conversely, freezing, condensation, or deposition (exothermic processes) release heat to the surroundings. These enthalpy changes, known as latent heats, are important in understanding the energetics of physical transformations and their impact on chemical systems.
14. What is the role of a catalyst in the thermochemistry of a reaction?
A catalyst does not change the overall enthalpy change of a reaction or its equilibrium position. Instead, it provides an alternative reaction pathway with lower activation energy, increasing the rate at which the reaction reaches equilibrium. While catalysts are crucial in kinetics, their primary impact in thermochemistry is indirect – they can affect how quickly a system reaches its final thermodynamic state without altering that state.
15. How does the concept of free energy (G) combine enthalpy and entropy in thermochemistry?
Gibbs free energy (G) combines enthalpy (H) and entropy (S) through the equation G = H - TS, where T is temperature. The change in free energy (ΔG) for a process determines its spontaneity: if ΔG < 0, the process is spontaneous; if ΔG > 0, it's non-spontaneous; if ΔG = 0, the system is at equilibrium. This concept allows prediction of reaction spontaneity by considering both the enthalpy change (ΔH) and entropy change (ΔS) of the reaction.
16. What is the significance of standard state in thermochemical calculations?
Standard state refers to a reference state for thermodynamic measurements, typically defined as 1 atm pressure for gases and 1 M concentration for solutions at 25°C. It's significant because it provides a consistent basis for comparing thermodynamic properties of different substances and reactions. Standard state values, denoted by a ° symbol (e.g., ΔH°), allow for accurate and reproducible calculations in thermochemistry.
17. How does the concept of bond energy relate to the enthalpy of reaction?
Bond energy is the energy required to break one mole of a particular type of bond in gaseous molecules. The enthalpy of reaction can be estimated by comparing the total bond energies of the reactants to those of the products. If the total bond energy of the products is less than that of the reactants, the reaction is exothermic, and vice versa. This concept provides insight into the relationship between molecular structure and reaction energetics.
18. What is the importance of calorimetry in thermochemistry?
Calorimetry is a technique used to measure the heat transferred in chemical reactions or physical processes. It's crucial in thermochemistry for determining enthalpy changes experimentally. Calorimeters, devices used in calorimetry, allow for the precise measurement of heat exchange between a system and its surroundings, providing direct empirical data for thermochemical calculations and validating theoretical predictions.
19. How does Le Chatelier's Principle apply to the thermochemistry of reversible reactions?
Le Chatelier's Principle states that when a system at equilibrium is disturbed, it will shift to counteract the disturbance. In thermochemistry, this principle applies to how temperature changes affect equilibrium. For exothermic reactions, increasing temperature shifts the equilibrium towards reactants (endothermic direction), while for endothermic reactions, increasing temperature favors products. This principle is crucial in understanding how temperature affects the position of chemical equilibria.
20. What is the relationship between reaction coordinate diagrams and activation energy in thermochemistry?
Reaction coordinate diagrams graphically represent the energy changes during a chemical reaction. They show the activation energy (Ea) – the minimum energy barrier that must be overcome for a reaction to proceed. In thermochemistry, these diagrams illustrate the relationship between the kinetics (activation energy) and thermodynamics (enthalpy change) of a reaction. They help visualize how catalysts lower activation energy without changing the overall enthalpy of the reaction.
21. How do intermolecular forces influence the thermochemistry of phase changes?
Intermolecular forces (e.g., hydrogen bonding, van der Waals forces) directly affect the enthalpy of phase changes. Stronger intermolecular forces result in higher enthalpies of vaporization and fusion because more energy is required to overcome these attractions. This concept explains why water, with its strong hydrogen bonds, has unusually high boiling and melting points compared to similar-sized molecules.
22. What is the significance of the Born-Haber cycle in thermochemistry?
The Born-Haber cycle is a theoretical approach used to calculate lattice energies of ionic compounds, which cannot be measured directly. It applies Hess's Law by breaking down the formation of an ionic solid into several steps with known enthalpy changes. This cycle is significant because it links observable thermochemical data with the theoretical concept of lattice energy, providing insights into the stability of ionic compounds.
23. How does the concept of resonance affect bond energies and reaction enthalpies?
Resonance occurs when a molecule can be represented by multiple Lewis structures. It typically leads to greater stability and lower overall energy of the molecule. In thermochemistry, resonance affects bond energies by distributing electron density, often resulting in bonds that are stronger than typical single bonds but weaker than full double or triple bonds. This impacts reaction enthalpies, as molecules with significant resonance often have lower heats of formation and are more stable.
24. What is the relationship between electrochemistry and thermochemistry?
Electrochemistry and thermochemistry are closely related through the concept of free energy. In electrochemical cells, the electrical work done is related to the change in Gibbs free energy of the reaction. The standard cell potential (E°) is directly related to the standard Gibbs free energy change (ΔG°) through the equation ΔG° = -nFE°, where n is the number of electrons transferred and F is Faraday's constant. This relationship allows for the calculation of thermodynamic parameters from electrochemical data and vice versa.
25. How does the concept of entropy explain the spontaneity of endothermic processes?
Endothermic processes, which absorb heat, can be spontaneous if they result in a significant increase in entropy. The Second Law of Thermodynamics states that the entropy of the universe always increases for spontaneous processes. For an endothermic process to be spontaneous, the TΔS term in the Gibbs free energy equation (ΔG = ΔH - TΔS) must be larger than ΔH, resulting in a negative ΔG. This often occurs in processes that increase disorder, such as the dissolution of some salts in water.
26. What is the importance of standard molar entropy in thermochemical calculations?
Standard molar entropy (S°) is the entropy of one mole of a substance in its standard state. It's important in thermochemical calculations because, unlike enthalpy, entropy has an absolute scale. Standard molar entropies can be used to calculate entropy changes in reactions (ΔS°rxn) by summing the entropies of products minus reactants. This value is crucial in determining the spontaneity of reactions, especially when combined with enthalpy changes in the Gibbs free energy equation.
27. How does the Third Law of Thermodynamics relate to absolute entropy?
The Third Law of Thermodynamics states that the entropy of a perfect crystal at absolute zero temperature is zero. This law provides a reference point for measuring absolute entropies of substances. It's significant in thermochemistry because it allows for the calculation of absolute entropy values, which are essential for determining entropy changes in reactions and understanding the spontaneity of processes at different temperatures.
28. What is the significance of Kirchhoff's law in thermochemistry?
Kirchhoff's law relates the temperature dependence of reaction enthalpies to the heat capacities of reactants and products. It states that the change in the heat of reaction with temperature is equal to the difference in heat capacities between products and reactants. This law is significant because it allows for the calculation of reaction enthalpies at different temperatures, which is crucial in many industrial and laboratory processes where reactions occur at non-standard temperatures.
29. How do solvent effects influence the thermochemistry of reactions in solution?
Solvent effects can significantly impact the thermochemistry of reactions in solution. The enthalpy of solvation, which is the heat released or absorbed when a solute dissolves, contributes to the overall enthalpy change of reactions in solution. Solvents can stabilize or destabilize reactants, products, or transition states through various interactions (e.g., hydrogen bonding, ion-dipole interactions), affecting both the kinetics and thermodynamics of reactions. Understanding these effects is crucial for accurately predicting and interpreting reaction energetics in solution.
30. What is the relationship between bond order and bond enthalpy?
Bond order, which represents the number of electron pairs shared between atoms, is directly related to bond enthalpy. Generally, as bond order increases, bond enthalpy also increases. This is because multiple bonds (double or triple) involve sharing more electrons, resulting in stronger attractions between atoms. For example, the C-C single bond has a lower bond enthalpy than a C=C double bond, which in turn has a lower bond enthalpy than a C≡C triple bond. This relationship is crucial in predicting and understanding the energetics of molecular transformations.
31. How does the concept of conjugate acid-base pairs relate to thermochemistry?
Conjugate acid-base pairs are related in thermochemistry through their relative strengths and the energy changes associated with proton transfer. The strength of an acid or base is reflected in its enthalpy of dissociation or protonation. Stronger acids have weaker conjugate bases and vice versa. This relationship affects the enthalpy changes in acid-base reactions and buffer solutions. Understanding these energetics is crucial in predicting the direction and extent of proton transfer reactions and their associated heat effects.
32. What is the significance of the Clausius-Clapeyron equation in thermochemistry?
The Clausius-Clapeyron equation relates vapor pressure to temperature and the enthalpy of vaporization. It's significant in thermochemistry because it allows for the calculation of enthalpies of vaporization from vapor pressure data at different temperatures, or vice versa. This equation is crucial in understanding phase transitions, particularly the behavior of liquids and gases, and is widely used in fields like atmospheric chemistry and chemical engineering.
33. How does the concept of lattice energy relate to the solubility of ionic compounds?
Lattice energy is the energy required to separate one mole of an ionic solid into its constituent gaseous ions. It's directly related to the solubility of ionic compounds: compounds with higher lattice energies tend to be less soluble because more energy is required to break the ionic bonds. The solubility process involves overcoming the lattice energy (endothermic) and the release of energy through hydration of ions (exothermic). The balance between these energies determines the overall enthalpy of solution and, consequently, the solubility of the compound.
34. What is the role of transition states in the thermochemistry of chemical reactions?
Transition states represent the highest energy configuration along the reaction coordinate between reactants and products. In thermochemistry, the energy of the transition state relative to the reactants determines the activation energy of the reaction. While transition states don't directly affect the overall enthalpy change of a reaction (which depends only on the initial and final states), they

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