AQUEOUS SOLUTIONS AND CHEMICAL EQUILIBRIA Flashcards

(60 cards)

1
Q

substances that have a natural positive or negative electrical charge when dissolved in water

A

Electrolytes

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2
Q

Ionized completely in a solvent

A

Strong Electrolytes

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3
Q

Ionized partially on solvent

A

Weak Electrolytes

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4
Q

produced in the reaction of an acid with a base - Examples include NaCl, Na2SO4, and NaOOCCH3 (sodium acetate)

A

Salt

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5
Q

acid is a proton donor, and a base is a proton acceptor - For a molecule to behave as an acid, it must encounter a proton acceptor (or base). Likewise, a molecule that can accept a proton behaves as a base if it encounters an acid.

A

Brønsted-Lowry Theory

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6
Q

formed when an acid loses a proton. For example, acetate ion is the conjugate base of acetic acid

A

Conjugate Base

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7
Q

formed when a base accepts a proton

A

Conjugate Acid

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8
Q

is the hydrated proton formed when water reacts with an acid

A

Hydronium Ions

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9
Q

species that have both acidic and basic properties

A

Amphiprotic Species

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10
Q

are an important class of amphiprotic compounds that contain both a weak acid and a weak base functional group

A

simple amino acids

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11
Q

a species that has both a positive and a negative charge

A

zwitterion

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12
Q

is the classic example of an amphiprotic solvent, that can act either as an acid or as a base depending on the solute.

A

Water

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13
Q

Other Common Amphiprotic Solvents

A

methanol, ethanol, and anhydrous acetic acid

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14
Q

(also called autoionization) is the spontaneous reaction of molecules of a substance to give a pair of ion

A

Autoprotolysis

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15
Q

reaction with the solvent is sufficiently complete that no undissociated solute molecules are left in aqueous solution

A

Strong Acids

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16
Q

react incompletely with water to give solutions containing significant quantities of both the parent acid and its conjugate base

A

Weak Acids

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17
Q

various acids dissociate to different degrees and have different strengths

A

Differentiating Solvent

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18
Q

everal acids are completely dissociated and show the same strength

A

Leveling Solvent

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19
Q

the ratio of concentrations of reactants and products is constant

A

Chemical Equilibrium

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20
Q

are algebraic equations that describe the concentration relationships among reactants and products at equilibrium

A

Equilibrium-constant Expressions

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21
Q

states that the position of an equilibrium always shifts in such a direction as to relieve a stress that is applied to the system
an increase in temperature of a system alters the concentration relationship in the direction that tends to absorb heat, and an increase in pressure favors those participants that occupy a smaller total volume

A

Le Châtelier’s Principle

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22
Q

a shift in the position of an equilibrium caused by adding one of the reactants or products to a system

A

Mass-action Effect

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23
Q

is a branch of chemistry that concerns the flow of heat and energy in chemical reactions. The position of a chemical equilibrium is related to these energy changes

A

Chemical Thermodynamics

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24
Q

resists changes in pH when it is diluted or when acids or bases are added to it

A

Buffer Solution

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25
The analyte is separated from a solution of the sample as a precipitate and is converted to a compound of known composition that can be weighed
Precipitation Gravimetry
26
the analyte is separated from other constituents of a sample by converting it to a gas of known chemical composition
Volatilization Gravimetry
27
the analyte is separated by deposition on an electrode by an electrical current The mass of this product then provides a measure of the analyte concentration
Electrogravimetry
28
the mass of a reagent of known concentration required to react completely with the analyte provides the information needed to determine the analyte concentration
Gravimetric Titrimetry
29
uses a mass spectrometer to separate the gaseous ions formed from the elements making up a sample of matter
Atomic Mass Spectroscopy
30
a stable phase showing little tendency to aggregate and separate from the aqueous phase
Colloidal Suspensions
31
composed of particles having large diameters about a tenth of a millimeter or greater
Crystalline Suspension
32
is the effect of light scattering in colloidal dispersion while showing no light in a true solution This effect is used to determine whether a mixture is a true solution or a colloid
Tyndall Effect
33
the ratio of the difference of the concentration of the reactants and the solubility of the precipitate to the solubility of the precipitate. Supersaturation ratio is defined as the supply rate of solute Q based on the growth rate in a quasisteady state
Relative Super Saturation
34
the initial process of the formation of a crystal. The crystals may form from solutions, liquids or from vapo
Nucleation
35
the process of increasing the size of a pre-existing crystal structure
Particle growth or crystal growth
36
Particle Growth or Crystal Growth in Three Stages
Nucleation Coalescent Coagulation Agglomeration
37
is an unstable solution that contains a higher solute concentration than a saturated solution. As excess solute precipitates with time, supersaturation decreases to zero
Supersaturated Solution
38
is a process in which a substance (gas, liquid, or solid) is held on the surface of a solid A
Adsorption
39
is retention of a substance within the pores of a solid
Absorption
40
Consist mainly of adsorbed ions
Primary Adsorption Layer
41
which contains sufficient excess of negative ions to just balance the charge on the surface of the particle
Counter – ion Layer
42
is a process by which a coagulated colloid returns to its dispersed state
Peptization
43
is a process in which a precipitate is heated in the solution from which it was formed (the mother liquor) and allowed to stand in contact with the solution
Digestion
44
is the solution from which a precipitate was formed
Mother Liquor
45
is a process in which normally soluble compounds are carried out of solution by a precipitate
Coprecipitation
46
Four Types of Coprecipitation
1. Surface Adsorption 2. Mixed – crystal Formation 3. Occlusion 4. Mechanical Entrapment
47
common source of coprecipitation and is likely to cause significant contamination of precipitates with large specific surface areas that is coagulated colloids
Surface Adsorption
48
a drastic but effective way to minimize the effects of adsorption
Reprecipitation
49
is a type of coprecipitation in which a contaminant ion replaces an ion in the lattice of a crystal
Mixed-Crystal Formation
50
- is a type of coprecipitation in which a compound is trapped within a pocket formed during rapid crystal growth
Occlusion
51
occurs when crystals lie close together during growth
Mechanical Entrapment
52
is a process in which a precipitate is formed by slow generation of a precipitating reagent homogeneously throughout a solution
Homogeneous precipitation
53
typically form slightly soluble salts or hydrous oxides with the analyte
Inorganic Precipitating Agents
54
loses electrons and is oxidized in a chemical reaction.
Reducing Agents
55
chemical compound that binds tightly to metal ions compounds typically contain at least two
Chelating Agents
56
cyclical metal-organic compounds in which the metal is a part of one or more five- or sixmembered rings.
Chelates
57
Widely Used Chelating Agents
8-Hydroxyquinoline (oxine) Dimethylglyoxime Sodium Tetraphenylborate
58
vary widely from cation to cation and are pH dependent because 8-hydroxyquinoline is always deprotonated during a chelation reaction.
8-Hydroxyquinoline (oxine)
59
is an organic precipitating agent of unparalleled specificity
Dimethylglyoxime
60
is an important example of an organic precipitating reagent that forms salt-like precipitates
Sodium Tetraphenylborate