General Chemistry Ch 9. Solutions Flashcards

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1
Q

Solutions

A

Homogenous mixtures composed of two or more substances, combine to form a single phase, generally the liquid phase

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2
Q

Solvent

A

Particles that surround solute particles via electrostatic interactions in a process called salvation or dissolution

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3
Q

Solute

A

Particles surrounded by solvent particles via electrostatic interactions in a process called solvation or dissolution

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4
Q

Solvation

A

aka dissolution, process where solvent particles surround solute particles via electrostatic interaction, most endothermic although dissolution of gas into liquid is exothermic

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5
Q

Dissolution

A

aka solvation, process where solvent particles surround solute particles via electrostatic interaction, most endothermic although dissolution of gas into liquid is exothermic

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6
Q

Aqueous solutions

A

-

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7
Q

Hydration

A

Solvation in water

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8
Q

Solubility

A

The maximum amount of solute that can be dissolved in a given solvent and a given temperature, it is often expressed as molar solubility

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9
Q

Molar solubility

A

The molarity of the solute at saturation

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10
Q

Complex ions

A

aka coordination compounds, composed of metallic ions bonded to various neural compounds and anions, referred to as ligands, formation of them increases the solubility of otherwise insoluble ions (opposite of common ion effect), formation of the involves electron pair donors and electron pair acceptors similarly to coordinate covalent bonding

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11
Q

Coordination compounds

A

aka complex ions, composed of metallic ions bonded to various neural compounds and anions, referred to as ligands, formation of them increases the solubility of otherwise insoluble ions (opposite of common ion effect), formation of the involves electron pair donors and electron pair acceptors similarly to coordinate covalent bonding

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12
Q

Coordinate covalent bonding

A

-

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13
Q

Percent composition by mass

A

Mass of solute per mass of solution times 100, used for aqueous solutions and solid in solid solutions

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14
Q

Mole fraction

A

Moles of solute per total moles, used for calculating vapor pressure depression and partial pressures of gases in a system

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15
Q

Molarity

A

Moles of solute per liters of solution, most common unit for concentration and is used for rate laws, the law of mass action, osmotic pressure, pH and pOH, and the Nernst equation

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16
Q

Molality

A

Moles of solute per kilograms of solvent, used for boiling point elevation and freezing point depression

17
Q

Normality

A

Number of equivalents per liters of solution, the molarity of the species of interest and is used for acid-base and oxidation-reduction reactions

18
Q

Saturated solutions

A

Are in equilibrium at that particular temperature

19
Q

Solubility product constant (Ksp)

A

Simple the equilibrium constant for a dissociation reaction

20
Q

Ion product (IP)

A

Can compare to Ksp to determine the level of saturation and behavior of the solution

21
Q

IP

A

The solution is unsaturated, and if more solute is added, it will dissolve

22
Q

IP=Ksp

A

The solution is saturated (at equilibrium) and there will be no change in concentrations

23
Q

IP>Ksp

A

The solution is supersaturated and a precipitate will form

24
Q

Formation or stability constant (Kf)

A

The equilibrium constant for complex formation, usually much greater than Ksp, increases the solubility of other salts containing the same ions because it uses up the products of those dissolution reactions, shifting the equilibrium to the right (opposite of common ion)

25
Q

Common ion effect

A

Decreases the solubility of a compound in a solution that already contains one of the ions in the compound, the presence of that ion in solution shifts the dissolution to the left, decreasing its dissociation

26
Q

Colligative properties

A

Physical properties of solutions that depend on the concentration of dissolved particles but not on their chemical identity

27
Q

Vapor pressure depression

A

Follows Raoult’s law, the presence of other solutes decreases the evaporation rate of a solvent without affecting its condensation rate, thus decreasing its vapor pressure, also explains boiling point elevation - as the vapor pressure decreases, the temperature (energy required to boil the liquid must be raised)

28
Q

Freezing point depression

A

Shift in the phase equilibria dependent on the molality of the solution

29
Q

Boiling point elevation

A

Shifts in the phase equilibria dependent on the molality of the solution

30
Q

Osmotic pressure

A

Primarily dependent on the molarity of the solution

31
Q

Van’t Hoff factor (i)

A

For solutions that dissociate, this can be used in freezing point depression, boiling point elevation, and osmotic pressure calculations