unit 1 Flashcards

1
Q

thermoregulation

A

The study of energy changes involved in physical and chemical processes.

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2
Q

First law of thermodynamics

A

The total energy of the universe is constant
Energy cannot be created or destroyed, only transformed from one substance to another and converted into various forms.

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3
Q

Potential energy:

A

Stored energy as a result of position or composition
Has the potential to do work

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4
Q

kinetic energy

A

Energy of motion
Energy AT WORK as a result of its motion.

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5
Q

thermal energy

A

internal energy of a substance due to the kinetic energy of its atoms and/ or molecules and chemical composition(bonds)

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6
Q

heat

A

amount of kinetic energy transferred between substances. Thus…an object CANNOT possess heat, only thermal energy.

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7
Q

Temperature

A

A measure of the average kinetic energy of entities in a substance

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8
Q

As particles move faster,

A

substance warms and vice versa

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9
Q

System

A

The part of the universe being studied.

In a chemical reaction, the system includes reactants and products.

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10
Q

Surroundings

A

Everything outside the system.

Essentially, the rest of the universe besides the system.

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11
Q

enthalpy

A

The total thermal energy (kinetic + potential) of a system at constant pressure.
Enthalpy cannot be measured absolutely, only enthalpy changes can be studied.

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12
Q

Enthalpy Change (ΔH)

A

Energy absorbed or released as the system changes from reactants to products.
Formula: ΔH = Hproducts - Hreactants

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13
Q

endothermic

A

Energy is absorbed.
Hproducts > Hreactants, so ΔH > 0 (positive).

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14
Q

exothermic

A

Energy is released.
Hproducts < Hreactants, so ΔH < 0 (negative).

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15
Q

Molar Enthalpy Changes (ΔHx)

A

The enthalpy change for a physical, chemical, or nuclear change involving 1 mole of a substance.
Determined experimentally (empirically).

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16
Q

What is a Calorimeter?

A

a device used to measure heat flow (enthalpy change) associated with a chemical or physical process.

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17
Q
  1. Simple (Coffee Cup) Calorimeter
A

Measures enthalpy change at constant pressure (open to atmosphere).
Water = surroundings.
Styrofoam insulates the system and immediate surroundings from greater surroundings.

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18
Q
  1. Bomb Calorimeter
A

Measures enthalpy change at constant volume.
The bomb (steel chamber) transfers heat to surrounding water.
The insulating container prevents heat exchange with the environment.

19
Q

Assumptions in Calorimetry

A

No heat is lost between the calorimeter and the environment.
Heat absorbed or released by the calorimeter itself is negligible.
A dilute aqueous solution behaves like pure water:
Density

20
Q

Energy Relationship (System & Surroundings)

A

Magnitude of heat transferred is the same, but the sign is opposite.

21
Q

Restricting the Surroundings in Calorimetry

A

Water represents the surroundings in calorimetry.
Exothermic reaction → Water absorbs energy.
Endothermic reaction → Water provides energy.

Dilute aqueous solution absorbs/releases energy → acts as both system & surroundings.

22
Q

Why Use Hess’s Law?

A

Some reactions release too much energy or occur too slowly for simple calorimetry.
Hess’s Law allows enthalpy change (Δ𝐻) to be determined without directly measuring it.

23
Q

What is Chemical Kinetics?

A

The study of reaction rates and the mechanisms by which reactions occur.
Focuses on how to speed up or slow down chemical reactions.

24
Q

Rate of Reaction

A

Determined by measuring:
- Rate of product formation
- Rate of reactant consumption
Measurable Properties:

Concentration
Mass
Colour
Conductivity
Volume
Pressure

25
Average Rate of Reaction Formula
Average Rate= Change in concentration/Elapsed time ​ Units: mol/L·s
26
Concentration Changes During a Reaction
Reaction rate is faster at the beginning and slows down over time. Graphing reaction data helps determine: Average rate of reaction Instantaneous rate of reaction
27
Representing Reaction Rates
Reactants: Have a negative sign (concentration decreases over time). Products: Have a positive sign (concentration increases over time).
28
Collision Theory
Particles are in constant random motion. Reactions occur when particles collide.
29
Types of Collisions:
Effective Collisions – Have sufficient energy & correct orientation, leading to a reaction. Ineffective Collisions – Lack energy or proper orientation, so no reaction occurs.
30
Factors Affecting Reaction Rate
Frequency of collisions (more collisions = faster reaction). Fraction of effective collisions (higher fraction = faster reaction).
31
Effective Collision Criteria
Correct Orientation Reactant molecules must collide with the right geometry. Sufficient Energy Particles must have enough energy to break old bonds & form new ones.
32
Energy Requirements for a Reaction
Threshold Energy: Minimum kinetic energy needed for a reaction to occur. Activation Energy (𝐸𝑎): Extra energy required to overcome the energy barrier.
33
Transition State Theory
Explains how molecules transition from reactants to products. Kinetic energy converts to potential energy during a reaction
34
Factors That Affect Reaction Rate
Chemical nature of reactants Concentration of reactants/products Surface area of reactants Temperature of the system Presence of a catalyst
35
Chemical Nature of Reactants
Rate depends on: Bond strength (stronger bonds → slower reaction). Molecular complexity (more complex → slower reaction). Threshold energy (higher energy required → slower reaction). Chemical Kinetics: Affects the fraction of effective collisions.
36
Concentration & Pressure
Higher concentration = more particles = more collisions = faster reaction. In gases, increasing pressure = increasing concentration. Chemical Kinetics: Affects the collision frequency.
37
surface Area (Heterogeneous Reactions Only)
Reactions occur at the surface of solids. Larger surface area = more collisions = faster reaction. Chemical Kinetics: Affects the collision frequency.
38
Temperature
Higher temperature = particles move faster & collide more forcefully. Increases: Collision frequency Fraction of effective collisions Chemical Kinetics: Affects both.
39
Catalyst
Speeds up reaction by lowering activation energy. Not consumed in the reaction. Types of Catalysts: Heterogeneous – Different physical state than reactants. Homogeneous – Same physical state as reactants. Chemical Kinetics: Affects the fraction of effective collisions.
40
What is the Rate Law?
Describes the quantitative relationship between reaction rate & reactant concentration. Shows how reaction rate depends on initial concentrations.
41
What is a Reaction Mechanism?
Most reactions do not occur in a single step. Reaction mechanism = a series of steps that make up the overall reaction.
42
Types of Collisions:
Unimolecular – 1 reactant molecule. Bimolecular – 2 reactant molecules. Termolecular – 3 reactant molecules (rare)
43
Reaction Intermediates
Molecules formed in one step & consumed in another. Do NOT appear in the overall reaction (cancel out).
44
Rate-Determining Step (RDS)
The slowest step in the mechanism. Controls the overall reaction rate (like a bottleneck in traffic).