Chapter 7- Thermochemistry Flashcards

1
Q

First law of thermodynamics

A

Change in U = Q - W

U= change in internal energy of system (directly proportional to temperature) 
Q= heat added to system 
W= work done by system
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2
Q

Isothermal

A

Constant temperature

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3
Q

Adiabatic

A

No heat exchanged between system and environment

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4
Q

Isobaric

A

Pressure is constant of a system

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5
Q

Isovolumetric

A

Aka isochoric. Experience no change in volume (neither expand nor compress) no work is done.

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6
Q

Standard conditions

A

25C (298K), 1atm, 1M concentrations

*used for measuring standard S, H, G, and electrochemical cell voltage

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7
Q

Standard temperature and pressure (STP)

A

0C (273K) and pressure is 1atm

*used for gas law calculations

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8
Q

Sublimation

A

Solid to gas

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9
Q

Deposition

A

Gas to solid

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10
Q

Critical point

A

No distinction between phases for this temp and pressure. (Supercritical fluids)

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11
Q

Zeroth law of thermodynamics

A

Objects are in thermal equilibrium only when their temperatures are equal

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12
Q

Enthalpy

A

(H) equivalent of heat under constant pressure. State function so path doesn’t matter for value.
+ endothermic
- exothermic

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13
Q

Calorimetry

A

Process of measuring transferred heat

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14
Q

Equation if no work is done

A

Qsystem = -Qsurroundings

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15
Q

When does the temperature change with respect to a phase change

A

The temperature stays the same until the whole compound changes phase. No temp change during freezing, melting, condensation, or vaporization until the process is complete.

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16
Q

Heat still changes during phase changes even tho temp does not. How do you calculate the heat change if temp change is zero?

A

With enthalpy
q = mL
m-mass
L- latent heat (general for enthalpy)

17
Q

Second law of thermodynamics

A

Energy spontaneously disperses from being localized to becoming spread out if it’s not hindered from doing so. (Entropy)

18
Q

Entropy equation

A

(S) = Qrev / T

Qrev- heat gained or lost in reversible process

19
Q

Entropy increase vs decrease

A

Increase- energy distributed into a system

Decrease- energy distributed out of a system

20
Q

Gibbs free energy equation

A

🔺G = 🔺H - T🔺S

Toward equilibrium means lower Gibbs (goal is lowest Gibbs)

21
Q

🔺G -, +, and 0

A
  • spontaneous
    + nonspontaneous
    0 state of equilibrium
22
Q

Standard free energy change equation

A

🔺G = -RT ln(Keq)

The larger Keq the more spontaneous the reaction

23
Q

Free energy change equation (not at standard state)

A

🔺G = RT ln(Q/Keq)

24
Q

Hear transfer during phase change

A

q = mL

25
Q

Spontaneous process moving in the forward direction

A

🔺GQ

26
Q

Endergonic vs exergonic

A

They both describe Gibbs free energy.

Exergonic- release energy, spontaneous, 🔺G>0