Acids and Bases Flashcards

1
Q

dissociate to produce an excess of hydrogen ions (H+) in solution; have H at beginning of formula

A

Arrhenius acid

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2
Q

dissociate to produce an excess of hydroxide ions (OH-) in solution; have OH at end of formula

A

Arrhenius base

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3
Q

species that can donate H atoms

A

Bronsted-Lowry acid

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4
Q

species that accept H atoms

A

Bronsted-Lowry base

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5
Q

electron pair acceptors

A

Lewis acid

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6
Q

electron pair donors

A

Lewis base

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7
Q

species that can behave as an acid (in a basic environment) or a base (in an acidic environment)

A

amphoteric

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8
Q

amphoteric species that donate or accept a proton (H+ ion), behaving as a Bronsted-Lowry acid or base

A

amphiprotic

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9
Q

amphiprotic example:

A

water- can accept a H+ to become H3O+ or lose a H+ to become OH-

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10
Q

process where an amphoteric compound reacts with itself (like water); one water molecule can donate a hydrogen atom to another water molecule to produce the hydronium ion (H3O+) and the hydroxide ion (OH-)

A

autoionization

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11
Q

water dissociation constant (K(w))

A

K(w) = [H3O+] [OH-] = 10^-14

true at 298 K, only affected by changes in temperature

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12
Q

logarithmic scale for the concentration of hydrogen (hydronium) ions

A

pH

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13
Q

pH

A

pH = -log [H+] = log 1/[H+]

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14
Q

logarithmic scale for the concentration of hydroxide ions

A

pOH

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15
Q

pOH

A

pOH = -log [OH-] = log 1/[OH-]

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16
Q

pH + pOH = __

A

pH + pOH = 14

in aqueous solutions at 298 K

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17
Q

completely dissociate into their component ions in aqueous solution

A

strong acids and bases

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18
Q

do not completely dissociate in solution and have corresponding dissociation constants (K(a) and K(b))

A

weak acids and bases

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19
Q

acid dissociation constant (K(a))

A

K(a) = [H3O+] [A-] / [HA]

20
Q

base dissociation constant (K(b))

A

K(b) = [OH-] [B+] / [BOH]

21
Q

acid formed when a base gains a proton

A

conjugate acid

22
Q

base formed when an acid loses a proton

A

conjugate base

23
Q

when an acid and base react with each other to form a salt and sometimes water

A

neutralization reaction

24
Q

defined as one mole of the species of interest

A

equivalent

25
Q

equal to one mole of H+ (H3O+) ions

A

acid equivalent

26
Q

equal to one mole of OH- ions

A

base equivalent

27
Q

the concentration of acid or base equivalents in solution

A

normality

28
Q

acids and bases that can donate or accept multiple electrons/protons (by the Bronsted-Lowry definition)

A

polyvalent/polyprotic

29
Q

used to determine the concentration of known reactant in a solution; performed by adding small volumes of a solution of known concentration (titrant) to a known volume of a solution of unknown concentration (titrand) until completion of the reaction is achieved at the equivalence point

A

titration

30
Q

titration:

has a known concentration and is added slowly to the titrand to reach the equivalence point

A

titrant

31
Q

titration:

has an unknown concentration but a known volume

A

titrand

32
Q

titration:
midpoint of the buffering region, in which half of the titrant has been protonated (or deprotonated); thus, [HA] = [A-] and a buffer is formed

A

half-equivalence point

33
Q

titration:
is indicated by the steepest slope in a titration curve; it is reached when the number of acid equivalents in the original solution equals the number of base equivalents added, or vice-versa

A

equivalence point

34
Q

equivalence point equation:

A

N(A) V(A) = N(B) V(B)

where:
N(A) and N(B) = acid and base normalities
V(A) and V(B) = volumes of acid and base solutions

35
Q

have equivalence points at pH = 7

A

strong acid + strong base titrations

36
Q

have equivalence points at pH > 7

A

weak acid + strong base titrations

37
Q

have equivalence points at pH < 7

A

weak base + strong acid titrations

38
Q

can have equivalence points above or below 7, depending on the relative strength of the acid and base

A

weak acid + weak base titrations

39
Q

titration:
weak acids or bases that display different colors in their protonated and deprotonated forms; ____ chosen for a titration should have a pK(a) close to the pH of the expected equivalence point

A

indicators

40
Q

titration:

when the indicator reaches its final color in a titration

A

endpoint

41
Q

titration:

observed in polyvalent/polyprotic acid and base titrations

A

multiple buffering regions and equivalence points

42
Q

consists of a weak acid and its conjugate salt or a weak base and its conjugate salt; they resist large fluctuations in pH; e.g. a solution of acetic acid (CH3COOH) and its salt, sodium acetate (CH3COO- Na+), or a solution of ammonia (NH3) and its salt, ammonium chloride (NH4+ Cl-)

A

buffer solutions

43
Q

refers to the ability of a buffer to resist changes in pH; maximal ____ is seen within 1 pH point of the pK(a) of the acid in the buffer solution

A

buffering capacity

44
Q

quantifies the relationship between pH and pK(a) for weak acids and between pOH and pK(b) for weak bases; when a solution is optimally buffered, pH = pK(a) and pOH = pK(b)

A

Henderson-Hasselbach equation

45
Q

Henderson-Hasselbach equation

A

pH = pK(a) + log [A-] / [HA]

pOH = pK(b) + log [B+] / [BOH]

where:
[A-} = concentration of the conjugate base
[HA] = concentration of the weak acid
[B+] = concentration of the conjugate acid
[BOH] = concentration of the weak base