Unit 1: Thermodynamics Flashcards

(48 cards)

1
Q

Thermochemistry

A

Study of energy changes.

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2
Q

Physical change

A

a change in a substances form.

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3
Q

Chemical change

A

Rearrangement of atoms to form new compounds.

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4
Q

Nuclear change

A

Change in protons/neutrons that results in the formation of new atoms.

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5
Q

Potential E

A

Energy stored in a object.

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6
Q

Kinetic E

A

Energy of motion.

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7
Q

Work

A

Force acting over a distance

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8
Q

Heat

A

Amount of thermal energy transferred between systems cuz of a temperature difference.

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9
Q

Endothermic

A

Energy is absorbed, temperature of surrounding environment lowers.

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10
Q

Exothermic

A

Energy is released, temperature of surrounding environment increases.

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11
Q

1st Law:

A

Energy cant be created or destroyed, only transferred or transformed.

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12
Q

2nd Law:

A

When 2 objects are in contact, heat is transferred from the hotter object to the cooler one until = same temperature.

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13
Q

Open system:

A

E and matter can be exchanged w/surroundings.

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14
Q

Closed system:

A

E but not matter can be exchanged w/surroundings.

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15
Q

Isolated system:

A

E and matter cant be exchanged w/surroundings.

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16
Q

Alpha decay:

A

Atom breaks down to 2p and 2n (mass decreases by 4 and atomic number decreases by 2) = new element.

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17
Q

Beta Particle:

A

a fast electron emitted during radioactive decay of an atoms nucleus.

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18
Q

Beta decay:

A

a neutron changes into a p and an e (the nucleus will have one less e but an extra p). Atomic number increases by 1, but mass stays same.

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19
Q

Gamma Decay:

A

After radioactive decay, nucleus emits extra energy as gamma rays - electromagnetic radiation w/high frequency.

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20
Q

Nucelar fusion:

A

when 2 light atoms fuse tg to create a heavier atom w/ the goal of generating E.

21
Q

Nucelar fission:

A

when a heavier nuclide splits into 2 or more pieces (releases E)

22
Q

Enthalpy (∆H):

A

Total E contained in a chemical system (PE & KE)

23
Q

Enthalpy of Solution:

A

1) bonds break b/t solutes and solvents so that attraction can occur. Change associated w/dissolving = ∆Hsolution

24
Q

Phase change and enthalpy:

A

Substance goes from more ordered to less ordered (s –> l) = Endothermic

Substance goes from less ordered to more ordered (l –> s) = Exothermic

25
Enthalpy change of rxn (∆Hr):
When bonds in reactants break: requires E --> endothermic When bonds form to make products: releases E --> exothermic
26
How to find Enthalpy
Using a calorimeter (double-walled vessel w/ a thermometer and stirring rod, filled w/H2O).
27
Assumptions of calorimeter
1) thermal E exchange b/t materials in vessel and outside can be ignored 2) heat capacity of water applies to any new solutions made 3) occurs under constant P
28
∆H˚r
Enthalpy change per mol for a reaction at SATP.
29
Hess Law
Enthalpy change is dependent only on the initial and final conditions.
30
Standard Molar Enthalpy of Formation: ΔH˚f
Amount of E absorbed/released when 1 mole of a compound is directly formed from its elements in there most stable state @ SATP.
31
Rate of a chemical rxn:
The speed @ which the [C] of a reactant/product changes. Dependent on frequency of collisions and how many of the collision are successful.
32
r = ?
Absolute value. Rate can be expressed as product formation or consumption.
33
Average rate of Rxn:
Speed at which reaction proceeds over time. Decreases overtime.
34
Instantaneous rate of Rxn:
Rate of rxn @ a particular point in time.
35
Methods to measure rxn rates:
1) Produce a gas (gas collected --> volume can be quantified as rxn proceeds) 2) Measuring Mass (total mass will be lost is gas is produced) 3) Rxns w/ions (measure the change in conductivity and plot it w/time) 4) Colour change (measure the intensity of colour using a spectrometer)
36
Collision theory
Chemical rxn always has particles that are moving @ diff speeds. Depends on the orientation and sufficent of Energy.
37
Effective and ineffective collision:
Effective: when particles have high energy and proper orientation to make new bonds. Ineffective: when particles bounce off each-other.
38
Transition state
Unstable structure formed during successful collisions b/t reactant particles. Always have a higher E lvl then prdts/rxnts.
39
Activated Complex (Ea)
Minimum E required for the activation complex to form and a successful rxn to happen. Lower the Ea --> faster the rxn.
40
Reaction Mechanism
Process by which a rxn occurs.
41
Factors that affect the rates of a rxn:
1) [C]: Higher = higher rate of rxn cuz theres more particles --> more collisions. 2) Surface area: Large SA --> faster rxn since more area is available for the solid to collide. 3) Temp: Higher temps increase the KE (speed of particles) so more collisions happen. 4) Catalyst: Lower the activation E req so rate increases.
42
Elementary step:
A step in a rxn mechanism that involves a single collision of 2-3 particles.
43
Intermediates:
Compounds that are produced and consumed.
44
Slowest elementary step:
Determines the rate of a rxn (rate determining step).
45
Rate law:
determined experimentally and expresses the relationship of the rate of rxn to the rate constant (k) + [C] of reactants raised to a power.
46
Rate order of 0:
[C] of rxnt doesn't affect the rate of rxn.
47
Rate order of a negative integer:
[C] INVERSELY affects the rate of rxn.
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Rate of positive integer:
[C] DIRECTLY affects the rate of rxn.