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What is the connection between Hess's law and the fact that \(H\) is a state function?

Short Answer

Expert verified
The connection between Hess's law and the fact that enthalpy (H) is a state function lies in their shared principle that their values depend only on the initial and final states of the system, irrespective of the path taken. Hess's law states that the total enthalpy change for a chemical reaction is the same, regardless of the path taken, as long as the initial and final states are the same. This concept is consistent with the nature of state functions like enthalpy, which depend only on the current state of the system and not the path taken to reach that state.

Step by step solution

01

Define Hess's Law

Hess's law states that the total enthalpy change for a chemical reaction is the same, regardless of the path taken, as long as the initial and final states are the same. This means that we can add or subtract intermediate reaction steps to find the overall enthalpy change for a given chemical reaction.
02

Define State Functions

State functions are properties in a system that depend only on the current state of the system, not the path taken to reach that state. In other words, the value of a state function at a specific point in time is independent of its history or how it got there. Some examples of state functions include enthalpy (H), internal energy (U), entropy (S), and Gibbs free energy (G).
03

Connect Hess's Law to State Functions

Now that we have defined Hess's law and state functions, we can establish the connection between them. Since enthalpy (H) is a state function, its value depends only on the initial and final states of a system. This matches the concept of Hess's law, which states that the total enthalpy change for a reaction is the same, regardless of the path taken, as long as the initial and final states are the same. In summary, the connection between Hess's law and the fact that enthalpy (H) is a state function lies in their shared principle that their values depend only on the initial and final states, irrespective of the path taken to get there.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Enthalpy Change
Enthalpy change, denoted by the symbol \( \Delta H \), is a measure of heat absorbed or released during a chemical process at constant pressure. It is a crucial concept in thermodynamics and a central part of understanding how energy is exchanged in chemical reactions.

Categorically, enthalpy change can be either endothermic, where the system absorbs heat (\( \Delta H > 0 \)), or exothermic, where it releases heat (\( \Delta H < 0 \)). A practical example would be the burning of natural gas in a boiler to produce heat; this reaction releases energy, hence it has a negative enthalpy change.

Understanding Enthalpy in Everyday Terms

Imagine making ice cubes in your freezer. The water loses heat as it freezes, an exothermic process. Conversely, boiling water for tea absorbs heat from the stove's burner, signaling an endothermic reaction.
State Functions
State functions are akin to your current location on a map; it doesn't matter whether you took the scenic route or the highway, your destination remains the same. In thermodynamics, these properties — such as enthalpy (\(H\)), internal energy (\(U\)), entropy (\(S\)), and Gibbs free energy (\(G\)) — depend only on the current state, not the journey to get there.

Think of climbing a mountain; your elevation (analogous to a state function) at the top is the same whether you hiked up or took a helicopter.

Why State Functions Matter in Chemistry

State functions help chemists predict the outcome of reactions and processes without concern for the specific pathway, offering a simplification in many calculative scenarios.
Chemical Reactions
Chemical reactions are the transformations where reactants convert into products. During reactions, bonds are broken and formed, a process that involves the exchange of energy. The enthalpy change is just one part of this complex dance.

The performance of a chemical reaction can be likened to a play with actors (molecules) and scenes (reaction steps). Each actor's entrance and exit represent the breaking and forming of bonds. The entirety of the play runs smoothly when all actors know the beginning and the end, but they're not worried about the order of events within.

Navigating the Landscape of Reactions

Understanding the balance of energy within these reactions is paramount for predicting not just the feasibility but also how much energy is required or will be released.
Gibbs Free Energy
Gibbs free energy, represented by \( G \), is a thermodynamic quantity that's used to predict the spontaneity of processes at constant temperature and pressure. It merges the concepts of enthalpy, entropy (\(S\)), and temperature (\(T\)) into one value, with its equation given by \( G = H - TS \).

A negative value of \( \Delta G \), or Gibbs free energy change, indicates a spontaneous process — it can occur without outside intervention. A positive value suggests a non-spontaneous process, which requires additional energy to proceed.

Gibbs Free Energy in a Nutshell

Just as a bank balance gives a quick insight into financial health, \( \Delta G \), enables us to immediately understand the 'energetic health' of a chemical process.

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Most popular questions from this chapter

(a) Write an equation that expresses the first law of thermodynamics in terms of heat and work. (b) Under what conditions will the quantities \(q\) and \(w\) be negative numbers?

(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 the volume of the system a state function? Why or why not?

(a) Why are fats well suited for energy storage in the human body? (b) A particular chip snack food is composed of \(12 \%\) protein, \(14 \%\) fat, and the rest carbohydrate. What percentage of the calorie content of this food is fat? (c) How many grams of protein provide the same fuel value as \(25 \mathrm{~g}\) of fat?

Identify the force present and explain whether work is being performed in the following cases: (a) You lift a pencil off the top of a desk. (b) A spring is compressed to half its normal length.

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 mol of \(\mathrm{O}_{2}\) and (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.

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