Matter: mixture and pure substance
Takes up space and has mass.
Can have variable composition (Mixture) or definite composition (Pure Substance).
Mixtures:
Heterogeneous: Not uniform throughout (e.g., suspension).
Homogeneous: Uniform throughout; also known as a solution.
Pure Substance:
Compound: Combination of two or more atoms (e.g., CO_2).
Element: Made up of atoms; cannot be futher separated by cannot be further separated by physical or chemical means.
Density:
Density increases from top to bottom in a substance.
Solution:
A homogeneous mixture made up of two parts: solute and solvent.
Can be any combination of two phases of matter.
Particles (atoms, ions, compounds) do not scatter light.
Suspension
A heterogeneous and mixture where a solid is not completely dissolved in a liquid.
Colloid: homo and hetero
Particles larger than molecules (solid in liquid, not completely dissolved).
Scatters light (e.g., fog).
Solution:
A homogeneous mixture
Solution = Solute + Solvent
Solute: Gets dissolved; lesser quantity (e.g., sugar).
Solvent: Does the dissolving; greater quantity (e.g., water is a universal solvent).
Solutes Classification:
Electrolytes: Yield dissolved ions (e.g., NaCl); conduct electricity.
Non-electrolytes: Yield dissolved molecules (e.g., sugar); do not conduct electricity.
Solvation:
Process of surrounding solute particles with solvent particles in aqueous solutions.
"Like dissolves like": Polar solvents dissolve polar solutes and ionic solutes; nonpolar solvents dissolve nonpolar solutes.
Polar solutes do not dissolve in nonpolar solvents, and vice versa.
Solvation in water is called hydration.
Definition: A measure of how much solute is dissolved in a given amount of solvent.
Qualitative Descriptions:
Dilute: Small amount of solute.
Concentrated: Large amount of solute.
Quantitative Measures:
Molarity (M)
Molality (m)
% by mass
ppm
Types of Solutions:
Unsaturated: Contains less solute than the solvent can hold; more solute can be added.
Saturated: Contains the maximum amount of solute a solvent can hold; precipitate forms at the bottom.
Supersaturated: Contains more solute dissolved than a saturated solution would contain under the same conditions.
Definition: The maximum amount of solute that can be dissolved in a solvent at a specific temperature (grams solute/100 g H_2O ).
Units: Typically grams solute / 100 g solvent.
Amount of substance required to form a saturated solution.
Factors Affecting Solubility:
Temperature:
Solids: Temperature increase = solubility increase.
Gases: Temperature increase = solubility decrease.
Pressure: Affects only gases; pressure increase = solubility increase.
Solubility Curves:
On the line = saturated solution.
Below the line = unsaturated solution.
Above the line = supersaturated solution.
Definition: Number of moles of solute per liter of solution (molar concentration).
Formula: M=\frac{\text{ mol solute}}{\text{L solution}}
Concentrated solutions of standard molarities are called stock solutions.
Solutions of lower concentrations are prepared by dilution.
As volume increases (more solvent added), molarity decreases.
Only the volume of solvent changes. moles of solute before= moles of solute after
Formulas:
M1V1=V1V2
Definition: Used when calculating colligative properties.
Formula: m=\frac{\text{ mol solute}}{\text{kg solvent}}
Be careful in identifying solute versus solvent (solvent usually has greater quantity).
Definition: Physical properties of solutions that depend ONLY on the number of solute particles present, NOT the kind of solute.
Ionic compounds have a larger effect than molecular compounds because when dissolved, they dissociate into multiple ions (electrolytes), while molecular compounds do not (non-electrolytes).
Examples:
Covalent; i=1
NaCl(s) \rightarrow Na^+(aq) + Cl^-(aq), i = 2 (electrolyte)
Four Colligative Properties:
Vapor Pressure Reduction:
Vapor pressure of a liquid is the equilibrium pressure of gas molecules from that liquid.
A solvent in a solution has lower vapor pressure than a pure solvent because it must overcome the attractive forces of both solvent and solute molecules.
Adding a solute lowers the solvent's vapor pressure.
Osmotic Pressure:
Osmosis: Flow of solvent through a semipermeable membrane from areas of low solute concentration to areas of high solute concentration.
Osmotic Pressure: Difference in pressure between pure solvent and solution once equilibrium is re-established.
Increases when the concentration of a solution increases
Boiling Point Elevation:
The boiling point of a solution is higher than that of the pure solvent.tb=Kbm\left(solution\right)i
For water, K_b = 0.512 \frac{°C}{m}.
Freezing Point Depression:
The freezing point of a solution is lower than that of the pure solvent.
tf=Kfm\left(solution\right)i
For water, K_f = 1.86 \frac{°C}{m}.
If the solution is ionic, write the dissociation equation to determine the i value.
Convert mass of solute to moles, and mass of solvent to kg, to calculate the molality (m).
Calculate boiling point +100
Calculate freezing point 0-x
A rate=speed
Average rate of a rxn= concentration over time
Chemical kinetics involves manipulating factors to speed up or slow down a chemical reaction.
Average rate of a reaction: \text{Rate} = \frac{\Delta \text{concentration}}{\Delta \text{time}}.
For a reaction to occur:
Reactant particles need to collide.
Some chemical bonds need to break, and new bonds need to form.
Not all collisions result in a new product.
The rate of a chemical reaction depends on the number of effective collisions between molecules.
Three parts to the collision theory:
Atoms or particles must collide.
They must collide at the correct orientation.
They must collide with a sufficient amount of energy.
Activation Energy (E_a):
The minimum amount of energy the colliding particles must have for productive collisions.
How fast or slow a reaction occurs depends on the magnitude of E_a.
Low E_a: Reaction is faster; higher number of productive collisions.
High E_a: Reaction is slower; lower number of productive collisions.
The more energy needed to bond, the fewer molecules will react.
Exothermic Reaction:
Releases energy.
Products have lower energy than reactants.
Endothermic Reaction:
Requires energy.
Products have higher energy than reactants.
Reaction rates are determined from experimental data, such as:
Change in volume
Change in mass
Change in concentration
Change in color
Change in pressure of gas produced
Nature of Reactants:
(Activity series of metals, halogens)
Certain chemicals are more reactive than others.
Ions, small molecules, and gas molecules react faster than liquids and large molecules.
Concentration of Reactants:
Lower concentration = fewer collisions = slower reaction rate.
Higher concentration = more collisions = faster reaction rate.
Surface Area:
Smaller surface area = fewer potential collision sites = slower reaction rate.
Larger surface area = more potential collision sites = faster reaction rate.
Temperature:
Higher temperature = faster reaction rate.
Higher temperature = more kinetic energy = more collisions (with more energy).
The increase of 10°C will cause the reaction rate to double.
Catalyst:
Increases the reaction rate without being consumed.
Lowers activation energy.
Biological catalysts: enzymes.
Inhibitors:
Slows down a reaction (e.g., food preservative).