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At what temperatures will the following processes be spontaneous? a. ΔH=18kJ and ΔS=60.J/K b. ΔH=+18kJ and ΔS=+60.J/K c. ΔH=+18kJ and ΔS=60.J/K d. ΔH=18kJ and ΔS=+60.J/K

Short Answer

Expert verified
a. T>300K b. T<300K c. No spontaneous temperature range d. Always spontaneous

Step by step solution

01

Convert units

Make sure all the units match. In this case, we'll convert ΔH from kJ to J: ΔH = -18 kJ × (1000 J/1 kJ) = -18,000 J Now we have ΔH = -18,000 J and ΔS = -60 J/K.
02

Solve for T

Use the Gibbs free energy equation and solve for T: ΔG < 0 ⇒ -18,000 - T(-60) < 0 Solve for T to find the temperature range. b. ΔH = +18 kJ and ΔS = +60 J/K Repeat Step 1 and Step 2 with given values. c. ΔH = +18 kJ and ΔS = -60 J/K Repeat Step 1 and Step 2 with given values. d. ΔH = -18 kJ and ΔS = +60 J/K Repeat Step 1 and Step 2 with given values.
03

Summary:

By solving for T in each case using the Gibbs free energy equation and the given values of ΔH and ΔS, we can determine the temperature ranges when each process will be spontaneous.

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Key Concepts

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

Spontaneity of Reactions
In chemistry, the spontaneity of a reaction indicates whether a reaction can occur without any external input. A spontaneous reaction naturally proceeds forward under certain conditions.
The spontaneity of a reaction is determined by the change in Gibbs free energy (ΔG). If ΔG<0, the reaction is spontaneous. Conversely, if ΔG>0, the reaction is non-spontaneous and requires additional energy to proceed.
It's important to understand that spontaneity does not necessarily mean that a reaction happens quickly. Instead, it refers to the thermodynamically favorable nature of the reaction.
  • A spontaneous reaction has negative ΔG
  • It releases free energy
  • Does not require external energy input
This concept helps us predict whether reactions will occur naturally and under what conditions, particularly regarding temperature and other influencing factors.
Thermodynamics
Thermodynamics is the branch of physical science that deals with the relations between heat and other forms of energy. It describes how energy moves and changes in different systems.
The main laws of thermodynamics are crucial for understanding how these processes work in chemistry. The first law, known as the law of energy conservation, states that energy cannot be created or destroyed—only transformed from one form to another.
Another critical aspect is the idea of equilibrium and how energy is distributed. Reactions occur because systems tend to move towards lower energy states. Thermodynamics helps us calculate these changes to determine if a reaction is feasible.
  • Relates to energy transfer and transformation
  • First law deals with energy conservation
  • Pivotal in understanding reaction potential
    Thermodynamics is a guiding principle in predicting whether chemical reactions occur, how they release or absorb energy, and their efficiency under specific conditions.
    Understanding this field provides a foundation for much of our knowledge of natural phenomena and aids in industrial applications where energy transformations are crucial.
Entropy
Entropy (S) refers to the measure of a system's disorder or randomness. In any process, entropy tends to increase, reflecting the universe's overall trend towards disorder.
In chemical reactions, changes in entropy (ΔS) can indicate whether a process will be spontaneous. Generally, reactions that increase entropy are more likely to be spontaneous.
Entropy is central to the second law of thermodynamics, which tells us that for any spontaneous process, the total entropy of the system and its surroundings increases.
  • Entropy measures disorder
  • An increase often indicates feasible reactions
  • Key to understanding the direction of energy transfer
Considering entropy provides insights into the probability of reactions occurring and helps us grasp the greater tendency of systems toward equilibrium with higher disorder.
Enthalpy
Enthalpy (H) is a concept used to understand the energy changes in a system, particularly during chemical reactions. It relates to heat exchange at constant pressure.
When reactions occur, changes in enthalpy (ΔH) are crucial to determine whether they release or absorb heat. Exothermic reactions, which release heat, have negative enthalpy changes (ΔH<0). On the other hand, endothermic reactions absorb heat, resulting in positive enthalpy changes (ΔH>0).
Enthalpy tells us about the heat content of a system and its changes when reactions are performed.
  • Measures heat content
  • Negative ΔH: Exothermic, heat released
  • Positive ΔH: Endothermic, heat absorbed
    Understanding enthalpy changes allows chemists to predict how reactions respond to different conditions, such as temperature fluctuations. It provides a detailed perspective on energy requirements and dynamics of reactions.

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Most popular questions from this chapter

Impure nickel, refined by smelting sulfide ores in a blast furnace, can be converted into metal from 99.90% to 99.99% purity by the Mond process. The primary reaction involved in the Mond process is Ni(s)+4CO(g)Ni(CO)4(g) a. Without referring to Appendix 4, predict the sign of ΔS for the above reaction. Explain. b. The spontaneity of the above reaction is temperature-dependent. Predict the sign of ΔSsurr for this reaction. Explain. c. For Ni(CO)4(g),ΔHf=607kJ/mol and S=417J/K mol at 298 K. Using these values and data in Appendix 4 calculate ΔH and ΔS for the above reaction. d. Calculate the temperature at which ΔG=0(K=1) for the above reaction, assuming that ΔH and ΔS do not depend on temperature.

Consider the reaction: H2S(g)+SO2(g)3S(g)+2H2O(l) for which ΔH is 233kJ and ΔS is 424J/K. a. Calculate the free energy change for the reaction (ΔG) at 393K. b. Assuming ΔH and ΔS do not depend on temperature, at what temperatures is this reaction spontaneous?

a. Using the free energy profile for a simple one-step reaction, show that at equilibrium K=kf/kr, where kf and kr are the rate constants for the forward and reverse reactions. Hint: Use the relationship ΔG=RTln(K) and represent kf and kr using the Arrhenius equation (k=AeEa/RT). b. Why is the following statement false? "A catalyst can increase the rate of a forward reaction but not the rate of the reverse reaction.”

For the process A(l)A(g), which direction is favored by changes in energy probability? Positional probability? Explain your answers. If you wanted to favor the process as written, would you raise or lower the temperature of the system? Explain.

Consider the reaction H2(g)+Br2(g)2HBr(g) where ΔH=103.8kJ/mol. In a particular experiment, equal moles of H2(g) at 1.00 atm and Br2(g) at 1.00 atm were mixed in a 1.00-L flask at 25C and allowed to reach equilibrium. Then the molecules of H2 at equilibrium were counted using a very sensitive technique, and 1.10×1013 molecules were found. For this reaction, calculate the values of K,ΔG, and ΔS.

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