Grade 12 AP Chemistry - Thermochemistry Terms + Initial Formulas

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Last updated 3:21 AM on 7/20/26
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62 Terms

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Energy

the capacity to do work or transfer heat

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Work

the E used to cause an object to move against a force

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Heat

E transfer from a hot object to a cold one

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Kinetic E

the E of motion

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Kinetic E Formula**************

Ek = ½mv2

where Ek = kinetic E in J

m = mass in kg

v = velocity in m/s

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Kinetic E increases as the speed of the object or its mass ________

increases

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Potential E

stored E

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Thermochemistry

study of the relationships between chemical rxns and E changes that involve heat

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Joule (J)

SI unit for E

1 J = 1kg-m2/s2

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Calorie (cal)

another unit for E

amount of E required to raise the temp of 1g of water by 1 degree C

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Conversion between cal and J

1 cal = 4.184 J

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Conversions between cal, Cal and kcal

1 Cal = 1000 cal = 1 kcal

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System

portion of the universe that is being studied for E changes

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Surroundings

everything else that is not the system

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Open vs Closed vs Isolated System

open: matter and E can be exchanged with the surroundings

closed: matter cannot be exchanged with the surroundings, but E can

isolated: neither matter or E can be exchanged with the surroundings

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Force

any push or pull exerted on an object

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Work formula (with F and d)*************

w = F x d

where w = work in J

F = force in kg-m/s2

d = distance in m

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First Law of Thermodynamics

E cannot be created or destroyed

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Internal E

sum of all kinetic + potential E in the system (+rotational, translational and vibrational movement of atoms)

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Change in internal E formula (not with q and w)

ΔE = Efinal - Einitial

where ΔE = change in internal E

Efinal = final internal E of the system

Einitial = initial internal E of the system

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a +ve value of ΔE means the system has ______ E from its surroundings

gained

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a -ve value of ΔE means the system has ____ E to its surroundings

lost

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Any increase in the E of the system results in a ________ in the E of the surroundings.

decrease

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Change in internal E formula (with q and w)

ΔE = q + w

where ΔE = change in internal E

q = heat in J

w = work in J

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q sign conventions

+ve = system gains heat

-ve = system loses heat

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w sign conventions

+ve = work done on system

-ve = work done by system

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ΔE sign conventions

+ve = net gain of E by system

-ve = net loss of E by system

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Endothermic

system absorbs heat

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Exothermic

system loses heat

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State Function

property of a system in which we only care about the before and after (and not how it got to the after)

e.g. internal E

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The value of a state function depends ONLY on the PRESENT state of the system, not the ____ the system took to reach that state.

path

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Chemical vs Physical vs Nuclear Change

chemical: new substance created

physical: change in state/shape

nuclear: change in the nucleus

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Fission vs Fusion

fission: splitting a larger atom into 2 or more smaller ones

fusion: joining 2 or more small atoms into a larger one

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Is fission or fusion more typically used today in nuclear power plants? Why is the other one not used?

fission is used

fusion is not used because it requires large amounts of E to sustain the high temp required for fusion

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Pressure-Volume Work

work involved in the expansion or compression of gases

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-ΔH represents

an exothermic change

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+ΔH represents

an endothermic change

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Thermochemical Equation

E value is included as a term in the chemical equation

<p>E value is included as a term in the chemical equation</p>
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Endothermic rxns ___________ heat, therefore the enthalpy term is written on the _______ side.

absorb/require, reactant

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Exothermic rxns ______ heat, therefore the enthalpy term is written on the _______ side.

release, product

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Potential E Diagram

graph where you put the reactants and products and indicate E levels

‘rxn progress’ goes on x-axis and ‘potential E, Ep (kJ)’ goes on y-axis

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The magnitude of ΔH is __________ to the amount of reactant.

proportional

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The forward rxn is equal in _________ but _________ in sign to reverse rxn’s ΔH.

magnitude, opposite

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ΔH varies with _____ of a substance…therefore you must specify it in chemical rxns.

state

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Calorimetry

measurement of heat flow

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Calorimetre

measures heat flow

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Heat Capacity (C)

amount of heat required to raise the temp of an object by 1 degree C

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Specific Heat Capacity (c)

amount of heat required to raise the temp of 1g of an object by 1 degree C

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Molar Heat Capacity (Cm)

heat capacity of one mol of a substance

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formula regarding ΔT, c, q and m

q = mcΔT

where q = heat E in J

m = mass in g

c = specific heat capacity in J/g degrees C

ΔT = change in temp

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Specific heat capacity of water

4.184 J/g degrees C

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Δ in Enthalpy (ΔH)

difference between E absorbed and E released when breaking/forming chemical bonds in rxns

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Thermal E

measure of the kinetic E of the particles in a system

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Heat

E transfer from hot to cold object

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Temperature

measure of the average kinetic E of the particles in a system

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ΔH formula regarding P, ΔV, ΔE***********************

ΔH = ΔE + PΔV

where ΔH = change in enthalpy (in ???)

ΔE = change in internal E (in J)

P = pressure (in ???)

ΔV = change in volume (in ???)

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Work formula (with P and ΔV)*************************

w = -PΔV

where w = work (in J)

P = pressure (in ???)

ΔV = change in volume (in ???)

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What are the units for heat capacity, C?

J/°C

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What are the units for specific heat capacity, c?

J/g°C

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What are the units for molar heat capacity, Cm?

J/mol°C

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Formula for ΔHtotal, n and ΔH

ΔHtotal = nΔH

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Formula with ΔHsystem and qsurroundings

ΔHsystem = ±|qsurroundings|