Year 2 - A level Flashcards

1
Q

What is needed for a dynamic equilibrium?

A

-Closed system, forward and backward reactions have same rate, conc. of products and reactions always constant(not equal)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is Le Chatilier’s principle?

A

When a change is applied to a system in dynamic equilibrium, the system shifts to oppose the change.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What 4 things affect equilibrium?

A
  • Temp. warmer shifts to endothermic
  • Conc.
  • Pressure
  • Catalysts (no shift just rate increase)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Conditions for Haber process?

A

450C at 200atm - compromise conditions with Iron catalyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Conditions for Hydration of ethene?

A

570k - compromise, 6000-7000kPa - high is good. Lots of steam not much ethene (cheaper)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Conditions for methanol formation?

A

520k, 5000-10000kPa, catalyst copper, zinc oxide and aluminium oxide.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Kc equation for aA + bB ⇌ cC dD

A

kc = [C]^c[D]^d/[A]^a[B]^b. If kc>1 eq lies to right as [Products]>[Reactants]

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Equation for partial pressure of a gas?

A

P(A) = no moles A/total moles x total pressure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Kp equation for aA + bB ⇌ cC dD when gases

A

p(C)^c p(D)^d/p(A)^a p(B)^b

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What acronym do you use when working out moles in equilibrium?

A

ICE - initial , change , equilibrium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What equation links ΔStotal, R and k?

A

ΔStotal = Rlnk when k is small, S is negative(unfeasible)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What equation links ΔG, R, T and k?

A

ΔG = -RTlnk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is a Bronsted-Lowrey base?

A

A proton acceptor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is a Bronsted-Lowrey acid

A

A proton donor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What does mono, di and tri-protic mean?

A

How many moles of protons per mole of acid.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What makes an acid stronger?

A

More dissociation

17
Q

What is key about weak acids?

A

They only partially dissociate

18
Q

Equation for PH?

A

PH = -log10[H+]

19
Q

Equation for [H+] from PH?

A

[H+] = 10^-PH

20
Q

Ka equation for weak acids?

A

Ka = [H+][A-]/[HA] as [H+] = [A-] in weak also Ka = [H+]^2/[HA]

21
Q

Equation for pKa?

A

pKa = -log10Ka

22
Q

Equation for Kw?

A

Kw = [H+][OH-] = 1x10^-14

23
Q

Equation for pKw?

A

pKw = -log10Kw

24
Q

What is a buffer solution?

A

One that can oppose change in PH when small quatities of acid or alkali are added.

25
Q

Rearrange Ka equation for [H+]

A

[H+] = √Ka x [HA]

26
Q

What is enthalpy of neutralisation?

A

Energy change when one mole of water is formed from acid and base under standard conditions

27
Q

What indicatiors should be used for combinations of strong/weak acids and strong/weak alkalis?

A

Both strong/weak - litmus
Strong acid, weak base - Methyl orange
Strong base, weak acid - Phenopthalein

28
Q

Equation for Kin?

A

Kin = [H+][In-]/[HIn] at halfway to end point [In-] = [HIn] so [H+] = KIn

29
Q

On a PH curve when does pKa = PH?

A

Halfway to the end point(equivalence point) [In-] = [HIn] so they cancel

30
Q

What are the 2 stages of enthalpy of solution?

A

-Break up the lattice, hydrate the ions

31
Q

What is atomisation energy?

A

Energy change for formation of one mole of gaseous atom from element in standard states.

32
Q

What is 1st electron affinity?

A

Energy change for addition of one electron for each mole of atoms in gas phase.

33
Q

What does Theory vs Experiment show for lattice energy calculations?

A

Theory assume perfect spheres so difference between two values shows polarisation = covalancey. Big difference more covalent.