5.1 Flashcards

1
Q

how do you calculate just normal rate

A

change in concentration/ time

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2
Q

how do you work out the overall order of an equation?

A

the sum of all the individual orders

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3
Q

how do you use half life to calculate rate constant?

A

k= ln2/half of time

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4
Q

what’s a clock reaction?

A

Measuring time taken for a visual change to occur to calculate how concentration affects rate

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5
Q

How do you determine k from a rate-concentration graph?

A

rate/ concentration

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6
Q

What is the rate determining step?

A

slowest step in a multi-step reaction

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7
Q

how does temp affect kp or kc?

A

If forward reaction is exothermic, an increase in temp would decrease k

If forward reaction is endothermic, an increase in temp would increase k

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8
Q

how does conc. and pressure affect kp or kc?

A

It doesn’t. The equilibrium can act to counteract the changes.

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9
Q

If k > 1

A

The equilibrium favours the right

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10
Q

If k < 1

A

The equilibrium favours the left

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11
Q

What’s a bronsted Lowry acid?

A

A proton donor

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12
Q

what’s a bronsted Lowry base?

A

A proton acceptor

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13
Q

Acid + alkali

A

-> salt + water

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14
Q

Acid + carbonate

A

-> salt + carbon dioxide + water

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15
Q

Acid + base

A

-> Salt + water

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16
Q

Acid + metal

A

-> salt + hydrogen

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17
Q

List all the strong acids you need to know for A level (6)

A

HCl (hydrochloric acid)
HNO3 (nitric acid)
H2SO4 (sulphuric acid)
HBr (hydrobromic acid)
HI (hydriodic acid)
HClO4 (chloric (VII) acid)

18
Q

What’s the acid dissociation constant?

A

measure of acid dissociation

19
Q

equation for Ka (strong acids)?

A

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

20
Q

how do you turn Ka to pKa and then back again

A

Ka -> pKa = -ln(Ka)

pKa -> Ka = 10^-pKa

21
Q

What does a high Ka suggest?

A

strong acid

22
Q

What does a high pKa suggest?

23
Q

How do you calculate pH?

24
Q

how do you calculate [H+] from pH?

25
What can we assume when calculating pH of strong acids?
that [HA] = [H+] this is because H+ completely dissociates
26
What can we assume when calculating pH of a weak acid?
that [H+] = [A-] as H+ and A- form at equal amounts due to weak acids only partially dissociating
27
Ka for weak acids?
[H+]^2 / [HA]
28
What are the limitations of the scientific estimations surrounding Ka?
It can be assumed that so little dissociation occurs in weak acids that initial[HA] ≃[HA]equilibrium If the sample is a stronger weak acid, this assumption is wrong
29
How would you practically determine the Ka of a weak acid?
Using a pH probe and the known conc. of the acid
30
What is the ionic product of water?
Kw = [H+][OH-]
31
Is water an acid or base? What does this mean for equilibrium
It's both. Can act as an acid by donating a proton: H2O ⟶ H+ + OH- Can act as a base by acting as a proton acceptor: H2O ⟶ H3O+ Therefore it's a constant exchange of protons so it is in equilibrium: H2O ⥭ H+ + OH-
32
How do you make a buffer? (Two ways)
1. A weak acid and its salt 2. Excess weak acid + strong alkali
33
If you add acid to a buffer, which way will equilibrium shift?
Left
34
If you add alkali to buffer, which way will equilibrium shift?
right
35
how do you calculate pH of a buffer
[H+] = Ka x [HA]/ [A-]
36
What's the buffer system of the blood?
H2CO3 -> H+ + HCO3-
37
What is the ideal blood pH, what are the conditions if too high or low?
7.35 - 7.45 too high- acidosis too low- alkalosis
38
what is the equivalence point of a titration?
The point at which the volume of one solution has reacted completely with the other and it matches the stoichiometry
39
what is the end point of the titration?
Equal concentrations of the weak acid and conjugate base forms of the indicator
40
What does the equivalence point look like on a graph?
The straight line
41
How do you calibrate a pH probe?
Wash it in deionised water Blott it dry Dip it in a solution of known pH and check its reading it properly