3.1.12 acids and bases Flashcards

(48 cards)

1
Q

bl acid

A

proton donor

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2
Q

bl base

A

proton acceptor

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3
Q

lewis acid

A

electron pair acceptor

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4
Q

lewis base

A

electron pair donor

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5
Q

conjugate base

A

acid that has donated its proton

so is now an honorary base kinda cause it has space to accept a proton

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6
Q

conjugate acid

A

base thats accepted a proton

honorary acid because can donate that proton

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7
Q

strong acid

A

completely dissociates when in solution

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8
Q

weak acid

A

partially ionises in solution

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9
Q

monoprotic acid

A

release 1 H+ per molecule

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10
Q

monobasic base

A

release 1 OH- per molecule

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11
Q

pH is defined as

A

the conc H+ ions present in a solution on a logarithmic scale

pH = -log[H+]

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12
Q

for every uncrease of 1pH the [H+] decreases by factor

A

10

so at pH 1, [H+] is 0.1

and at 2 it is 0.01

etc

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13
Q

when finding the pH of a strong acid

A

find [H+]
make sure to chekc acid is mono di tri

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14
Q

to find [H+] from pH

A

[H+] = 10^-pH

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15
Q

working out pH of diluted acid

A

moles are same

so find new [H+] by doing moles divided by new volume (c1v1=c2v2)

and find pH

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16
Q

pH always given in

A

2dp

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17
Q

Kw is

A

the ionic product of water

water partially ionises because it can act as a bl acid or base

H2O <–> H+ + OH-

the Kw is gotten from getting the Kc expression for this reversible reaction

Kc = [H+][OH-] / [H2O]
Kc x [H2O] = [H+][OH-]

constant x constant = constant. [H2O] is basc constant because barely any ionise

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18
Q

Kw at 25 c or 298k

A

1 x 10^-14

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19
Q

why does Kw change with temperature

A

Kc changes with temperature

and the f reaction is endothermic so more dissociation

so if Kc is changed and the []s are changed then Kw will change

this is why as temps rise water gets more acidic but it is still neutral because [H+]=[OH-]

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20
Q

finding pH of strong acid and strong base mixed together

A

moles of H+ and OH-

who is limiting? subtract their moles from the moles of excess to get moles remaining of whoever was in excess

finding [] of whoevers remaining by doing remaining moles / total volume

if OH- excess then use ioninc product of water

if H+ in excess use pH eq directly

21
Q

if they say pH change

A

find initial pH

ending pH so the changes in moles after whatevers been added

THE DIFFERENCE between them

22
Q

pH of a weak acid

A

weak acid dissociation constant, Ka

Ka = [H+][A-] / [HA]

and because its alone and ONLY BECAUSE ITS ALONE

the weak acid approximation

Ka = [H+]^2 / [HA]

23
Q

why must use ka for weak acids

A

they dissociate reversibly and partially

therefore reversible reaction of

HA <=> H+ + A-

24
Q

a large Ka means

A

eqm lies more to the left

bigger numerator and smaller denominator therefore more dissociation so its a stronger acid

25
small Ka
eqm lies more to right less dissociation, weak acid is moreso in protonated form so weaker acid
26
pKa
log of Ka pKa = -log(Ka) and you can get Ka from pKa value because Ka = 1o^-pKa
27
what does it mean if **pKA** is large
WEAKER ACID because a large Ka gives a small pKa, just like a large [H+] gives a small pH value
28
units of Ka!!!!
like Kc or Kp cancel out units of eq make sure check if want units
29
when HA is reacted with strong base
HA + OH- --> A- (+H2O) for every 1 mole of OH-, 1 mole of HA is reacted and 1 mole of A- is formed **if OH- in excess** use Kw **if HA in excess** use weak acid DISSOCIATION constant
30
titration
31
neutralisation
32
equivalence point
moles H+ = moles OH- you should be able to tell when this is by colour change of an indicator therefore indicator must be sharp colour change at certain pH
33
whats usually an indicator and why
weak acid because their partial ionisation means there is protonated and deprotonated forms in solution and colour change when one becomes other so used in titration bc when acid added for ex eqm shifts to decrease H+ by shifting to protonated form, HA. when HA > A-, colour change and if titrating in OH-, shifts to oppose change by more H+ to react with the OH- so more deprotonated. when A- > HA, colour change the titration basc forces the eqm to one side so get a colour change
34
endpoint
when colour change ideally equivalence and endpoint should be same. this is why depending on what titrating, choice of indicator changes
35
characteristics of good indicator
colour change is sharp and distinct no ambiguity on when changes endpoint = equiv point
36
SA SB
equiv point ~~ 7 sharp increase in pH (if flask is acid) as get closer to endpoint large vertical section on pH curve signifies equiv point
37
WA SB the start of it half neutralisation
equiv point above 7 buffer region resists changes to pH when small amounts of acid or alkali are added at equiv point, this is neutralisation. thevolume of base added here, half it. the pH at half neutralisation is the pKa so you can find Ka from pKa then identify WA from that because each WA have own Ka
38
SA WB
equiv below 7
39
WA WB
gradual increase in pH so no sharp change in pH so cant titrate with indicator because there will be no sharp colour change
40
when sketching pH curves
- whos in flask therefore where gonna start up or down - calculate initial pH with given info - calculate end pH - see if WA SB or whats the combination - have equiv point above at or below 7 based on the combination
41
a buffer is
a solution that resists large changes in pH when small amounts of acid or alkali are added to it or when it is diluted
42
how to make a buffer
WEAK ACID AND ITS SALT - so add them together just like that - or add limited amount of strong base which will be used up and form salt WEAK BASE AND ITS SALT - so add them together just like that - or add limited amount of strong acid which will be used up and form salt
43
how do acidic buffers work
[HA] and [A-] are much much higher than [H+] so when
44
finding the pH of a buffer
[H+] = [HA] / [A-] this is the dissociatio constant rearranged for H+ and Ka removed because its a constant the pH of the buffer depends on the ratio of [HA]:[A-] A- is from salt
45
when OH is added to acidic buffers
HA <=> H+ + A- reacts with H+ therefore H+ decreases so shifts to replace lost H+ so more dissociation so [ha] decreases slightly and [a-] increases slightly so ratio remains fairly constant
46
when H+ is added to acidic buffers
shifts to decrease H+ so in direction of b reaction so more protonation of A- [ha] increases slightly [a-] decreases slightly so ratio remains fairly constant
47
when h2o added to either buffer (dilution)
HA and A- diluted by same amount so ratio remains the same
48
for basic buffers see notes
see notes