Chem 1A Midterm 2- Energy

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Last updated 4:06 AM on 3/14/26
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157 Terms

1
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Law of conservation of mass

Mass (atoms/matter) can’t be created or destroyed

2
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In a balanced chemical equation, there should be (same/different) number of each element on either side

Same

3
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When balancing a chemical equation, what part do you change to balance?

Stoichiometric coefficient

4
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What are tips for balancing a chemical equation?

  1. Start with balancing whatever is in the fewest formulas

  2. Balance polyatomic ions as a single element

5
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What is the limiting reactant?

The reactant that runs out first, stopping the reaction and limiting how much product is made

6
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What is the opposite of the limiting reactant?

Excess

7
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T/F: You cannot have fractional stoichiometric coefficients

False- you can, since the coefficients represent ratios and not the whole amount of each element

8
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How do you find the limiting reactant?

Use unit conversion to find how much product can be made with either reactant, whichever makes the LEAST amount of product is the limiting reactant

9
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What is heat capacity?

(C) how much energy is needed to raise temperature

10
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What unit is temperature in, in heat capacity?

J/mol

11
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What is specific heat?

(c) heat capacity per g or mol

12
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What unit is specific heat in?

J/ g C

or

J/ mol C

13
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(Heat capacity/specific heat) is impacted by volume

Heat capacity is impacted by volume

Specific heat is not

14
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What is a factor in specific heat, in the case of liquids and solids?

Bonding strength/ IMFs

15
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What are degrees of freedom?

Ways for a molecule to move when influenced by heat energy

16
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What are the ways something can move, according to degrees of freedom?

Rotations

Vibrations

Translations

17
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Which kind of movement increases temperature?

Translations ONLY

18
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If something rotates or vibrates, it has a higher ____

Specific heat

19
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More degrees of freedom means a (higher/lower) final temp

More degrees of freedom means a lower final temp

20
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If something moves more, it will be (more/less) hot

If something moves more, it will be less hot

21
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If something moves less, it will be (more/less) hot

If something moves less, it will be more hot

Since most of its energy can go into translational movement, which would increase the T

22
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(More/less) bonds means more vibrations

More bonds means more vibrations

23
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What kind of bonds limit rotations?

Linear bonds

24
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(Weaker/stronger) IMFs make a molecule easier to move, resulting in (low/high) heat capacity and (low/high) temperature

Weaker IMFs make a molecule easier to move, resulting in low heat capacity and high temperature

25
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What are the equations for heat input/output?

q = mcΔT or q = CΔT

26
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What do the variables in q = mcΔT and q = CΔT stand for?

q - heat input or output

m - mass in mol

c - specific heat

C - heat capacity

ΔT - change in temperature (final - initial)

27
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In calorimetry, what two values are always the same between the surroundings and object?

Final temperature

28
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In calorimetry, how is q (heat input/output) related to either object?

The q of one object is the inverse of the other; or in other words

q (surroundings) = - (q object)

Because the amount of heat one object loses is the same amount as what the other gains

29
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What is the q of an exothermic reaction?

q < 0

30
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Which way does energy flow in an exothermic reaction?

Energy exits the system

31
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How does an exothermic reaction feel?

Hot!

32
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Which way do KE and PE flow in an exothermic reaction?

High → low

33
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What is the q of an endothermic reaction?

q > 0

34
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What is the flow of energy in an endothermic reaction?

Energy ENTERS system

35
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How does an endothermic reaction feel?

Cold!

36
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What is the flow of KE and PE in an endothermic reaction?

Low → high

37
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Which reaction has an energy input?

Endothermic

38
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Which reaction has an energy output?

Exothermic

39
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What is sublimation?

Phase change from solid to gas

40
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What does potential energy (at least in this class) refer to?

How close particles are to one another

41
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What sign is attraction?

Negative

42
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What sign is repelling?

Positive

43
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A small radius/close together particles indicate a (weak/strong) attraction and (very/less) negative PE

A small radius/close together particles indicate a strong attraction and very negative PE

44
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A large radius/far apart particles indicate a (weak/strong) attraction and (very/less) negative PE

A large radius/far apart particles indicate a weak attraction and less negative PE

45
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On a phase change graph, what does an angled slope indicate?

KE change, temperature change

46
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On a phase change graph, what does a constant slope indicate?

PE change, phase change

47
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Explain why PE change does not change temperature

Temperature will increase until a phase change, when another particle movement overtakes translation and causes temp to be constant during phase changes

48
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What is enthalpy?

Heat, ΔH

49
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T/F: ΔH of opposite phase changes are the same integer

F: ΔH of opposite phase changes are opposite integers

ex) ΔH(vaporization) = -ΔH(condensation)

50
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When looking for which system has lower PE, what can you look for?

  • Phase

    • From highest to lowest PE: gas, liquid, solid

  • Bond #

    • More bonds = more attractions = negative PE

51
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<p>Describe what is happening in this image, and how it relates to attraction/repulsion</p>

Describe what is happening in this image, and how it relates to attraction/repulsion

Read the graph from right to left

1) The distance (radius) decreases, and not much attraction is “felt” because particles are too far apart

2) The potential energy drops suddenly (indicating strong attraction!) when the particles are at optimal distance

3) As the radius decreases further, repulsion force dominates attraction force, and potential energy increases (strong repulsion)

4) Repulsion force will cause radius to increase to an optimal distance

52
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<p>Where on the graph do particles “want” to be?</p>

Where on the graph do particles “want” to be?

Particles want to be at the lowest PE possible, at a distance that is not too close or far

53
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What is optimal bond length?

Just the right length of bond so that repulsion does not over take attraction

54
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What is optimal bond energy?

The amount of energy input, in kJ/mol, required to break bond

55
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What makes a strong bond?

  • Higher order (more bonds)

  • More polar (a more polar bond indicates very partial charges that are attracted to one another)

  • Shorter bond length (look at the atom size)

56
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<p>When comparing two bonds’ attraction/repulsion graph, what can you look for?</p><p>(example pictured)</p>

When comparing two bonds’ attraction/repulsion graph, what can you look for?

(example pictured)

  • Radius: a shorter bond length will be closest to the axis (smaller r = stronger attraction)

  • Depth of curve, which represents bond strength (deeper curve = more PE, stronger attraction)

57
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T/F: Energy is stored in bonds, and breaking those bonds releases energy

False!! Common misconception, though :D

58
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Bond breaking is (endothermic/exothermic)

Bond breaking is endothermic

It requires energy input to break the bonds

59
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How can bond breakage release energy?

Forming an even stronger bond

60
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Which characteristics does low PE correspond with?

  • (Negative/positive)

  • (Strong/weak) attraction

Low PE = negative = strong attraction

61
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Which characteristics does high PE correspond with?

  • (Negative/positive)

  • (Strong/weak) attraction

High PE = positive = weak attraction

62
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What sign is an exothermic ΔH(rxn)?

ΔH(rxn) < 0

or

ΔH(rxn) is negative

63
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What sign is an endothermic ΔH(rxn)?

ΔH(rxn) > 0

or

ΔH(rxn) is positive

64
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In an exothermic reaction, products have (higher/lower) PE and (higher/lower) bond energies

In an exothermic reaction, products have lower PE and higher bond energies

65
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In an endothermic reaction, products have (higher/lower) PE and (higher/lower) bond energies

In an endothermic reaction, products have higher PE and lower bond energies

66
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What does Hess’s Law say?

If a reaction can be written as a sum of several steps, the ΔH is equal to the sum of Δ of each step

<p>If a reaction can be written as a sum of several steps, the ΔH is equal to the sum of Δ of each step</p>
67
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What is a pure element?

The most stable version of an element @ 1 atm and 298 K

68
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What state of matter are most elements in at standard conditions? What about noble gases?

Most elements are solids at standard conditions

Noble gases are gases

69
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Which elements want to be “doubled” at standard conditions?

H O N Cl Br F

70
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What is enthalpy of formation? aka ΔHfo

Heat energy released or consumed when 1 mol of substance is formed from pure elements in the most stable form @ standard state

71
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What unit is enthalpy of formation in?

kJ/mol^-1

72
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What is important to note about pure elements in ΔHfo equations?

Pure elements ΔHfo = 0 since you don’t form anything with pure elements (they’re already pure, as the name suggests)

73
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What is the ΔHrxno equation?

ΔHrxno = ∑nΔHof(product) - ∑nΔHof(reactants)

aka

[number of mols (enthalpy of formation of products)] - [number of mols (enthalpy of formation of reactants)]

74
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Given the three ways below to model PE or KE changes, which model corresponds to which energy change?

q = mcΔT

ΔHfus/con/vap

ΔHrxn

KE: q = mcΔT

PE: ΔHfus/con/vap and ΔHrxn

75
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Is enthalpy alone enough to predict the spontaneity of changes?

No!

76
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What is spontaneity?

The “natural” direction of change

77
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Is spontaneity always +ΔH?

No- can be +ΔH, -ΔH, or ΔH = 0

78
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What is entropy (S)?

Dispersion/spread of matter and energy

79
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How is entropy measured?

The number of ways you can arrange a system

80
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Many ways to arrange a system = (higher/lower) entropy

Higher

81
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Fewer ways to arrange a system = (higher/lower) entropy

Lower

82
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What is a perfect crystal, and what are its conditions?

Perfect crystals occur at T = 0 K, there is no entropy

83
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What is the ΔS of everything other than a perfect crystal?

S > 0

84
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When comparing entropy, what can you look at?

  • Phase of matter

    • # of particles

    • Which is hotter

  • # of molecules

  • Spread

85
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Arrange phases of matter by entropy, high to low

Gas > liquid > solid

86
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If both objects are gases, what can you look at to determine higher entropy?

Which has more particles

More particles = higher entropy

87
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If both objects are solids, what can you look at to determine higher entropy?

Which is hotter

88
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Do more or less molecules signal higher entropy?

More

89
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Does less or more spread out particles signal higher entropy?

More spread

90
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What is the equation for ΔSorxn?

ΔSorxn = ∑nSoproducts - ∑nSoreactants

91
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What does a negative ΔS indicate?

Nonspontaneous

92
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What does a positive ΔS indicate?

Spontaneity

93
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What is the relationship between ΔSsurr and ΔHsys?

ΔSsurr and ΔHsys are always the opposite sign of each other

94
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Are ΔSsurr and ΔSsys always opposite signs from one another?

No! They can be, but it’s not a rule

95
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What is the equation for ΔS using ΔH and T?

ΔS = ΔH/T

96
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When should you use ΔS = ΔH/T?

Constant T, like during a phase change

97
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What is the equation for ΔStotal?

ΔSsurr + ΔSsys = ΔStotal

98
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What sign is ΔStotal?

Should always be ΔStotal > 0

99
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What is the second law of thermodynamics?

Changes occur so universal entropy increases, aka so that ΔStotal is positive

100
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If ΔStotal is positive, it is (nonspontaneous/spontaneous)

If ΔStotal is positive, it is spontaneous

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