Exam 1 Study Material: Thermodynamics Flashcards

1
Q

What is energy a measure of and what are the different types of energy?

A

Energy is a measure of a system’s ability to do stuff. There are two types: potential and kinetic. Potential energy is associated with position and composition whereas kinetic energy is a measure of motion

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2
Q

What is Coulomb’s law dependent on?

A

Coulombs law is dependent on potential energy —> r is distance between particles

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3
Q

Which phase of matter has the highest KE has the highest KE and which variable (T, P, V, n) is most closely related to KE?

A

Gases have the highest KE and Temperature is most closely related to KE

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4
Q

At phase transitons which has the highest KE, liquid or gaseous water and why?

A

At the phase transition, both phases are at the same TEMPERATURE so they have the same KE

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5
Q

Which phase of water, liquid or gas has the smallest PE and why?

A

Liquid water has the smallest amount of PE because particles are closer leading to stability

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6
Q

What are the two ways that a system gains and loses energy?

A

A system loses or gains energy through heat (δq) and work (δw). δq represents a change in heat, representing the amount of thermal energy added to or removed from a system. δw is mechanical energy done by or on the system.

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7
Q

What does it mean when δq is negative? positive?

A

δq is negative when heat is lost by the system and absorbed by the surroundings. δq is positive when heat is absorbed by the system and lost by the surroundings.

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8
Q

What does it mean when δw is negative? positive?

A

δw is negative when a gas expands, so the system does work on the surroundings. δw is positive when a gas is compressed, so the surroundings does work on the system.

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9
Q

What type of motion is δw and δq?

A

δq is random motion while δw is ordered motion

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10
Q

What equation describes δq and units?

A

δq= moles x resistance to heating x temperature change (=molJ/molKK=J)

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11
Q

How do we define a system and surroundings?

A

The system is the component that undergoes an energy change; and acts. The surroundings is the component that responds to that action and enables the system to undergo that change.

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12
Q

What is kinetic molecular theory?

A

KMT explains how gas particles move and interact to give us the macroscopic properties we observe, like pressure and temperature, using ideal gases as the model.

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13
Q

Can we know the KE of each gas particle?

A

No! We can only know the average molar KE because it is not practical to measure the instantaneous speed of all gas particles

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14
Q

What is the equation for urms and what does it tell us?

A

Urms=sqrt(3RT/Mw) with R equaling 8.314 J/molK. It tells us that light gases at high temperatures move fastest

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15
Q

What does the R value mean in the urms equation?

A

R is the amount of work done by 1 mol of an deal gas upon changing its T by 1 K at fixed P

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16
Q

At constant P, what property changes with T?

A

Volume must increase with temperature.

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17
Q

On a Boltzmann graph, where can you find Urms and why?

A

Urms will be found to the right of the speed where the highest number of atoms are traveling because there are more atoms at a higher speeds than lower speeds.

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18
Q

How does the Urms graph of a gas moving fast look? moving slowly?

A

A graph that displays a fast-moving gas will be broad and shifted to the right. A slow-moving gas will be shifted left and will appear narrow.

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19
Q

What does temperature tell us?

A

T tells us how fast particles are moving

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20
Q

At constant volume, what is the work response from a gas that absorbs heat?

A

δq=+ and δw=0 since work is constant

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21
Q

What is the heat capacity of an ideal gas when volume is constant?

A

When volume is constant, Cv= 3/2R. That number represents an ideal gas’s resistance to a heat change at constant volume

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22
Q

How does the heat capacity at constant volume change for a real gas compared to an ideal gas?

A

Real gases have more forms of motion which means that they have a greater amount of ways to store their energy leading to a great Cv/ resistance to a heat change

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23
Q

What does heat and work together sum up to?

A

Together, heat and work sum up to the amount of internal energy (ΔE) of a system. ΔE=δq+δw

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24
Q

What is the first law of thermodynamics?

A

Heat can neither be created nor destroyed. The TOTAL energy of the universe is constant —> conservation of energy

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25
Q

What type of functions are heat and work? Internal energy?

A

Heat and work are path functions where as internal energy is a state function.

26
Q

What is the difference between a path and state function?

A

A path function involves physical quantities that depend on the path taken from the initial to the final state. A state function are physical quantity that is independent of the path taken from the initial to the final state.

27
Q

What does Cv correspond to for an ideal gas?

A

Cv= 3/2R comes from gas KEavg changing

28
Q

Why is Cp greater than Cv?

A

It requires more energy to change the temperature when the system is able to do work, thus, the gas has a greater resistance to a temperature change

29
Q

What is the value of Cp?

A

Cp= 5/2R for an ideal gas

30
Q

What is a constant volume calorimetry and how does it work?

A

Constant volume calorimetry (measurement of heat change) is a measure of ΔE through measure δq because at constant volume, work is not able to done

31
Q

What leads to a greater Cv?

A

Cv becomes greater as we introduce more ways to store thermal energy

32
Q

What is Cv related to? Which phases of matter tend to have higher heat capacities and why?

A

Cv is related to the ways a substance stores its energy through motion or IMFs. Generally, liquids>solid>real gases> ideal gases. Since liquids have both IMF and many ways to store their energy, they tend to have the greatest heat capacities

33
Q

How does heat resistance relate to bonds?

A

In bonds with similar structures, as you increase the number of bonds, you increase the heat capacity

34
Q

Describe the energetic interaction of a a hot piece of metal is dropped into a cold water

A

The metal will release heat that the water absorbs . Because of the first law of thermodynamics, -δqmetal=δqwater

35
Q

When a hot piece of metal is dropped into cold water, at what point will heat stop being transferred?

A

Heat transfer will stop when both bodies are at the same temperature—>(thermal equilibrium)

36
Q

What is one way that we can calculate ΔE at constant V?

A

We can calculate ΔE by directly measuring ΔT through bomb calorimetry

37
Q

How does bomb calorimetry work?

A

Bomb calorimetry involves placing a sample in a sealed container (the bomb), igniting it to undergo combustion, and measuring the resulting temperature change in water surrounding the bomb. By calculating this heat change and considering the heat capacity of the calorimeter, scientists can determine the heat of combustion for the tested substance, providing insights into its energy content.

38
Q

What is defined as the system and the surroundings for bomb calorimetry?

A

The system is the bomb contents —> reaction and the surroundings are the bomb walls and water

39
Q

Why do reactions release heat?

A

Reactions release heat in the form of potential energy because the bonds of the product are stronger than reactants

40
Q

Under what conditions do most chemical reactions take place?

A

Most chemical reactions take place under constant pressure, rather than constant volume

41
Q

What type of function does q become under constant pressure?

A

Under constant pressure, δq becomes a state function —>ΔH

42
Q

How is ΔH defined?

A

ΔH is the heat change associated with a chemical/physical process at constant pressure

43
Q

How are ΔH and ΔE similar?

A

Both ΔH and ΔE account for chemical bond energy, IMF energy, and energy of motion. They are both state functions that describe a heat change

44
Q

What differentiates ΔH from ΔE?

A

ΔH accounts for the energy of interaction with the environment, so it considers the fact that some heat is dissipated upon expansion

45
Q

What equation describes ΔH and explain how does it work?

A

ΔH= ΔH+PΔV. This equation has another PΔV that aims to account for the energy loss due to expansion

46
Q

What are two scenarios in which ΔH and ΔE differ?

A

Production or loss of a gas in a chemical reaction leads to ΔH<ΔE.>ΔE</ΔE.>

47
Q

What do we assume when calculating δw in chemical reactions?

A

Gas production is the only source of ΔV

48
Q

When are ΔH and ΔE equal to each other?

A

When the reaction does not involve gases, they are equal

49
Q

What must change with volume when calculating for δq at constant pressure?

A

At constant pressure, we assume the number of moles changes—-> δq=-PextΔV=-RTΔn

50
Q

What is coffee cup calorimetry and how can we tell when work is done?

A

Coffee cup calorimetry includes an insulated system where an aqueous phase reaction serves as the system and the water is the surroundings. Ccal=4.184. work is done through displacement of surrounding molecules

51
Q

If two moles of a reaction occur, how does ΔH change?

A

Since ΔH is per mole of reaction, when the moles are doubled, ΔH value is also doubled

52
Q

What happens to ΔH when a reaction goes the reverse way?

A

The magnitude of ΔH stays the same, however, the sign changes

53
Q

What is Hess’s Law?

A

Hess’s law tell us that if a reaction is carried out over multiple steps, ΔH for the nET reaction equals the sum of ΔH for each step.

54
Q

What does Hess’s law use to its advantage?

A

Hess’s law uses the first law of thermodynamics and ΔH being a state function

55
Q

How can we predict whether a reaction will be endothermic or exothermic?

A

Atoms bond to gain stability so if the products are more stable than the reactants, the reaction will be exothermic

56
Q

What is Bond Dissociate Energy?

A

BDE is the energy required to split a chemical bond in half

57
Q

What is the sign of ΔH when a reaction is endo vs exothermic?

A

ΔH is + when the reaction is endothermic and bonds are broke ΔH is - when a reaction is exothermic and bonds are formed

58
Q

What can we use to predict the energetic driving force of a reaction?

A

We can use bond dissociation energy and hess’s law

59
Q

What is the relationship between BDE, Bond order, and Bond length?

A

As Bond order increases, BDE increases, and bond length decreases

60
Q

Which type of bonds are most stable?

A

σ are the most stable type of bond

61
Q

How does BDE change as the number of bonds go up?

A

BDE increases as the number of bonds go up due to the stability gained when atoms bond together

62
Q

How can we solve for ΔHrxn?

A

ΔH= ΣΔHbonds broken - ΣΔHbonds formed