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Calculate ΔE and determine whether the process is endothermic or exothermic for the following cases: (a)q=0.763 kJ and w=840 J. (b) A system releases 66.1 kJ of heat to its surroundings while the surroundings do 44.0 kJ of work on the system.

Short Answer

Expert verified
In case (a): ΔE = -0.077 kJ, making the process exothermic. In case (b): ΔE = -22.1 kJ, also making the process exothermic.

Step by step solution

01

Calculate ΔE using ΔE = q + w

For this case, we're given values for q and w. We just need to plug these values into the equation: ΔE = q + w. Note that q and w have different units, so we need to make sure they have the same units before addition. w is given in Joules (J), while q is given in kilojoules (kJ). We can convert w to kJ by dividing it by 1000. So, ΔE = (0.763 kJ) + (-840 J * 1 kJ/1000 J) ΔE = 0.763 kJ - 0.84 kJ
02

Determine whether the process is endothermic or exothermic

Now that the units are the same, we can calculate ΔE: ΔE = -0.077 kJ Since ΔE is negative, the process is exothermic. Case (b):
03

Determine the signs of q and w

We're given that the system releases 66.1 kJ of heat to its surroundings, which means q = -66.1 kJ (heat released is negative). We're also given that the surroundings do 44.0 kJ of work on the system, which means w = +44.0 kJ (work done on the system is positive).
04

Calculate ΔE using ΔE = q + w

With the signs of q and w determined, we can calculate ΔE: ΔE = q + w ΔE = (-66.1 kJ) + (44.0 kJ)
05

Determine whether the process is endothermic or exothermic

Now we can calculate ΔE: ΔE = -22.1 kJ Since ΔE is negative, the process is exothermic.

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Key Concepts

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

Endothermic Processes
In thermochemistry, endothermic processes are characterized by the absorption of heat from the surroundings into the system. During such processes, the system gains energy, leading to an increase in internal energy, often reflected by a positive change in enthalpy ΔH.
To identify an endothermic reaction, look for cues such as:
  • Heat being added to the system
  • A positive value for heat change (q>0)
  • The process feeling cold to the touch as heat is absorbed from the environment
For example, melting ice is an endothermic process because it requires heat to change from a solid to a liquid form. The key indicator of endothermicity is the sign of the energy change, where ΔE or the enthalpy change is positive.
Exothermic Processes
Exothermic processes occur when a system releases heat to its surroundings. In these processes, the system loses energy, which is manifesting as a negative change in internal energy ΔE or enthalpy ΔH.
An easy way to recognize exothermic reactions is by their outcomes:
  • There is a release of heat, resulting in the surroundings becoming warmer
  • The change in energy (q) is negative, indicating heat being released (q<0)
  • These processes often feel hot to the touch
A classic example of an exothermic process is the combustion of gasoline, where heat is released, powering engines and producing an increase in temperature around the reaction zone. It's important in thermochemical calculations to determine whether a process is exothermic or endothermic by examining the sign of ΔE. A negative ΔE implies energy is released, confirming the process is exothermic.
Energy Change Calculation
Calculating the change in internal energy ΔE of a system is fundamental in thermochemistry. The formula to find ΔE is ΔE=q+w, where:
  • q represents the heat exchanged with the surroundings
  • w is the work done on or by the system
To perform the calculation, ensure both q and w are in the same units. Most commonly, q and w are measured in joules (J) or kilojoules (kJ). If needed, convert the units so they match.
For instance, solving the energy change from our examples:
1. For the first case, the conversion is necessary because w is in joules and needs to be converted to kilojoules before combining it with q using the equation:
ΔE=(0.763 kJ)+(840 J×1 kJ1000 J)=0.763 kJ0.84 kJ
This results in ΔE=0.077 kJ, and since it's negative, the process is exothermic.
2. Similarly, for the second case:
ΔE=(66.1 kJ)+(44.0 kJ)=22.1 kJ
Again, the negative result affirms that this is an exothermic process. The computation of ΔE not only reveals the direction of energy flow but also helps in understanding the nature of the process involved.

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Most popular questions from this chapter

When an 18.6-g sample of solid potassium hydroxide dissolves in 200.0 g of water in a coffee-cup calorimeter (Figure 5.18), the temperature rises from 23.7 to 44.5C. (a) Calculate the quantity of heat (in kJ) released in the reaction. (b) Using your result from part (a), calculate ΔH (in kJ/mol KOH) for the solution process. Assume that the specific heat of the solution is the same as that of pure water.

Three hydrocarbons that contain four carbons are listed here, along with their standard enthalpies of formation:  Hydrocarbon  Formula ΔHf0( kJ/mol) Butane C4H10(g)125 1-Butene C4H8(g)1 1-Butyne C4H6(g)165 (a) For each of these substances, calculate the molar enthalpy of combustion to CO2(g) and H2O(l) (b) Calculate the fuel value, in kJ/g, for each of these compounds. (c) For each hydrocarbon, determine the percentage of hydrogen by mass. (d) By comparing your answers for parts (b) and (c), propose a relationship between hydrogen content and fuel value in hydrocarbons.

(a) What is the electrostatic potential energy (in joules) between two electrons that are separated by 460pm? (b) What is the change in potential energy if the distance separating the two electrons is increased to 1.0nm ? (c) Does the potential energy of the two particles increase or decrease when the distance is increased to 1.0nm ?

Can you use an approach similar to Hess's law to calculate the change in internal energy, ΔE, for an overall reaction by summing the ΔE values of individual reactions that add up to give the desired overall reaction?

(a) Use enthalpies of formation given in Appendix C to calculate ΔH for the reaction Br2(g)2Br(g), and use this value to estimate the bond enthalpy D(BrBr). (b) How large is the difference between the value calculated in part (a) and the value given in Table 5.4 ?

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