Book: Ch. 6 Flashcards

1
Q

Define: thermodynamics

A

Study of energy and its transformations.

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2
Q

Define: thermochemistry

A

Branch of thermodynamics that deals with heat in chemical and physical change.

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3
Q

Define: system vs. surroundings [in thermodynamics]

A

System: the part of the universe we are focusing on.
Surroundings: everything else.

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4
Q

Define: internal energy (E) of a system

A

The sum of all the energies of all the components of a system.

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5
Q

What is the equation for change in the internal energy of a system?

A

∆E = E_final - E_initial = E_products - E_reactants

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6
Q

Define: heat (q)

A

Thermal energy. The energy transferred as a result of a difference in temperature between the system and the surroundings.

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7
Q

What is the equation for the total change in a system’s internal energy in terms of q and w?

A

∆E = q + w

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8
Q

Define: law of conservation of energy (first law of thermodynamics)

A

∆E_universe = ∆E_sys + ∆E_surroundings = 0

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9
Q

Define: joule (J)

A

SI unit of energy. 1 J = 1 kg m²/s²

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10
Q

Define: calorie (cal)

A

1 cal = 4.184 J

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11
Q

Define: state function

A

A property dependent only on the current state of the system, not on the path the system takes to reach that state. Examples: internal energy, composition, pressure, volume, temperature.

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12
Q

Define: pressure-volume work (PV work)

A

A type of mechanical work done when the volume of the system changes in the presence of an external pressure: w = -P∆V

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13
Q

Define: enthalpy (H)

A

For reactions at constant pressure, enthalpy eliminates the need to deal with PV work. H = E + PV

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14
Q

Define: change in enthalpy (∆H)

A

Change in the system’s internal energy plus the product of the pressure and the change in volume: ∆H = ∆E + P∆V

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15
Q

How is ∆H related to heat?

A

∆H = q_p, or enthalpy equals the heat absorbed or released at constant pressure.

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16
Q

Define: exothermic process

A

Releases heat as a product. Decrease in the enthalpy of the system: ∆H < 0

17
Q

Define: endothermic process

A

Absorbs heat as a reactant. Increase in the enthalpy of the system: ∆H > 0

18
Q

Define: heat capacity (C)

A

The quantity of heat required to change the temperature of an object by 1 K: q/∆T = constant = heat capacity (C) [J/K]

19
Q

Define: specific heat capacity (c)

A

Quantity of heat required to change the temperature of 1 gram of a substance or material by 1 K: specific heat capacity (c) = q/m∆T [J/gK]

20
Q

Given the specific heat capacity of an object being heated, the mass or temperature change can be found along with the heat absorbed by what equation?

A

q = cm∆T

21
Q

Define: molar heat capacity (C_m)

A

Quantity of heat required to change the temperature of 1 mole of a substance by 1 K: C_m = q/n∆T [J/mol K]

22
Q

Define: calorimeter

A

A device used to measure the heat released or absorbed by a physical or chemical process.

23
Q

What is a coffee-cup calorimeter?

A

For processes that take place at a constant pressure, heat transferred may be measured with one of these: you use the equation -q_sys = q_water [in the calorimeter]

24
Q

How is the heat released during the combustion of a sample measured with a bomb calorimeter?

A

-q_rxn = q_calorimeter, where q_calorimeter = C_calorimeter ∆T_calorimeter

25
Q

Define: thermochemical equation

A

Balanced equation that includes the enthalpy change of the reaction (∆H).

26
Q

Define: Hess’s law

A

∆H_overall = ∑ ∆H_i

27
Q

Define: standard states

A

Established set of specific conditions used to reduce the number of variables when studying a reaction.

28
Q

Define: standard enthalpy of a reaction

A

∆Hº_rxn is the enthalpy change of a reaction when it is measured at the standard state. It is also called the standard heat of reaction.

29
Q

Define: formation equation

A

1 mol of a compound forms from its elements. Like C + 2H₂ → CH₄

30
Q

Define: standard enthalpy of formation

A

∆Hº_f is the enthalpy change for a formation equation when all the substances are in their standard states.

31
Q

What is the equation for the standard enthalpy of a reaction?

A

∆Hº_rxn = ∑m∆Hº_f (products) - ∑n∆Hº_f (reactants), where m and n are the amounts of products and reactants given by the coefficients in the balanced equation.