Unit 3 Flashcards

(28 cards)

1
Q

titration

A

-the slow addition of one solution of a known concentration (called a titrant) to a known volume of another solution of unknown concentration
-acid/analyte is unknown, but the base/titrant is known, so by finding equivalence point, you can deduce amount of acid

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2
Q

indicator

A

-typically a weak acid that has different colors in dissociated and undissociated states
-changes colors as equivalence point

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3
Q

equivalence point

A

-point where the acid/base has been completely neutralized
-moles of acid and moles of base are equal
-determined through analyzing titration graph

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4
Q

End point

A

-point of titration when indicator changes color
-visible marker
-pH = pKin

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5
Q

Kin

A

-indicator constant
-Kin = [H3O][In-] / [HIn]

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6
Q

indicator equilibrium

A

-HIN(indicator) + H2O -> H3O+ + In-

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7
Q

pKIn

A

-pH - pKin = log([In-]/[HIn])
-similar to hendersson hasselbach
-when pH < pKin (acidic), it is initial color (color A)
-when pH = pKin, it is mixture (color A + B)
-when pH > pKin (basic), it is final color (color B)

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8
Q

titrant

A

-strong acid/base (typically base)
-known value, added to analyte

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9
Q

-analyte

A

-can be strong or weak acid/base (typically acid)
-unknown value, titrant is added to analyte

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10
Q

Strong acid and strong base

A

-Start: calculate pH by M of H3O (moles/L), usually equal to M of solution added
-Half: moles of H3O - moles of OH = new moles of H3O, then calculate pH from new M of H3O
-Eq: pH = 7
-past eq: calculate pH using M of OH (moles/L)

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11
Q

Weak acid and strong base

A

-start: use ICE table to find M of H3O and then pH
-half: usually equal to pKa, find M of OH added and then plug in values into hendersson hasselbach
-eq: number of moles of acid and base are equal, find pH by finding M of OH created by hydrolysis of base and Kb
-past eq: M of OH (moles/L)

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12
Q

monoprotic acid

A

-an acid capable of donating at most one hydrogen ion per molecule

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13
Q

polyprotic acid

A

-an acid capable of donating more than one hydrogen ion per molecule
-pH is calculated by filling out ICE table for each respective reaction (donation of H to H2O) and adding M of H3O produced to get pH
-ex. H2S (H2S and HS- can both be an acids)
-has twice the neutralization power of monoprotic acid

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14
Q

amphiprotic anion/salt

A

-a salt whose anion can serve as both a weak acid and a weak base
-pH = 1/2 (pKa1 + pKa2)
-ex. NaHS, HS can be acid or base

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15
Q

Saturated solution

A

-a solution in equilibrium with a solid solute

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16
Q

Supersaturated solution

A

-describes a solution that temporarily contains more solute than the equilibrium quantity
-will return by precipitating solid out of solution

17
Q

Solvate

A

-process of surrounding solute molecules with solvent molecules

18
Q

Solubility

A

-amount of solute that dissolves in a fixed volume of a given solvent at a given temp
-depends on temp and pH

19
Q

Insoluble

A

ionic compound with solubility < 0.1 g/L

20
Q

Slightly soluble

A

ionic compounds with solubilities between 0.1-10 g/L

21
Q

Soluble

A

ionic compounds with solubilities >10 g/L

22
Q

Ksp

A

-solubility product
-the equilibrium constant for the dissolution of a slightly soluble salt
-Ksp = [A+][B-] (when AB -> A+ + B-)

23
Q

Molar solubility (S)

A

-S^2 = Ksp
-how many g of a salt dissolve per liter of water
-turned into gram solubility by multiplying S by molar mass of salt

24
Q

Q

A

-reaction quotient
-Q = [A+][B-] (before any reaction occurs)
-predicts whether a precipitate will form when two solutions are mixed
-Q< Ksp, no precipitate will form
-Q> Ksp, precipitate will form until Q has reached Ksp

25
Common ion effect
-the observation that if a solution and a solid salt to be dissolved in it have an ion in common, the solubility of the salt is depressed -allows us to calculate solubility of sparingly soluble salt in a solution that contains a given concentration of a common ion -Concentration of the common ion at equilibrium is the sum of its concentration initially present and the additional amount produced in dissolution of solid
26
Corollary to common ion effect
-when one of the ions reacts and is consumed, it causes additional salt to dissolve -increases solubility of salt
27
pH and solubility
-solubilities of metal hydroxides (OH) increase at lower pH -solubilities of salts with anion of weak base increase at lower pH (H consumes anion)
28
Selective precipitation of ions
-two elements with a common anion and widely different solubilities -add enough of common anion to precipitate all of less soluble compound and leave more soluble in solution -max amount is found by keeping Q of soluble under Ksp value