TOPIC 13 - Energetics II Flashcards

1
Q

What is lattice enthalpy of formation?

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

What is enthalpy chaange of atomisation?

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

What is 1st electron affinity?

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

What is 2nd electron affinity?

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

Why are Born-Haber cycles useful?

A

To calculate enthalpies that can’t be measured experimentally.

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

What is A?

A

Enthalpy of formation

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

What is B?

A

Enthalpy of atomisation of chlorine

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

What is C?

A

Enthalpy of atomisation of lithium

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

What is D?

A

1st ionisation energy of lithium

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

What is E?

A

1st electron affinity of chlorine

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

What is F?

A

Lattice enthalpy of formation of LiCl

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

Calculate lattice enthlapy of LiCl using the Born-Haber cycle

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

What is a perfectly ionic model?

A

Ions are evenly spherical in the latticeand the charge is evenly distributed (point charge)

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

Why are all the experimental values higher than the theoretical ?

A

None of them is purely ionic. There is some covalent character. The electron cloud in the anion is distorted so electrons are closer to the +ve charge, so more energy is released.

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

Are smaller cations more or less polarising? Why?

A

More polarising.

In smaller cations, the +ve charge is closer to the electrons in the anion and so electrostatic forces of attraction are greater and the electron cloud is distorted more.

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

Are cations with bigger charge more or less polarising?

A

More polarising.

Bigger charge = bigger electrostatic forces of attraction = electron cloud in anion is distorted more.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Are bigger anions more or less polarisable? Why?

A

More polarisable.

Electron cloud is further away from the nucleus of the anion and so electrons are more attracted to the nucleus of the cation, so electron cloud is more distorted.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the general rule for electronegativity in the periodic table?

A

Further up and right you go, electronegativity increases (excluding nobel gases).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

How does difference in electronegativity affect the nature (ionic/covalent) of the bond?

A

The bigger the difference between the two atoms, the more ionic the bond is.

20
Q

What is enthalpy change of solution?

A
21
Q

What happens, in terms of bonds, for a substance to dissolve?

A

Substance bonds break - endothermic.

Bonds fromed between solvent and substance - exothermic.

22
Q

For a substance to dissolve, what must the strength of the newly formed bonds be?

A

Same strength or greater than those broken previously.

23
Q

What enthalpy of solution does a soluble substance have?

A

-ve enthalpy of solution (exothermic).

24
Q

What is enthalpy of hydration?

A
25
Q

What is A?

A

Enthalpy change of solution

26
Q

What is B?

A

Lattice dissociation enthalpy

27
Q

What is C?

A

Enthalpy of hydration

28
Q

How does the charge of the ions affect enthalpy of hydration?

A
29
Q

How does size of ions affect the enthalpy of hydration?

A
30
Q

What is entropy?

A

The number of ways energy can be spread out between particles. It is a measure of disorder in a system.

31
Q

Can an enthapically unfavourable reaction be spontaneous (feasible)?

A

Yes. If the change in entropy overcomes the change in enthalpy

i.e.

32
Q

What is the equation for the entropy change of a reaction?

A
33
Q

What are the standard conditions for standard entropy?

A
34
Q

Does entropy increase or decrease in an entropically feasible reaction?

A

Increases.

35
Q

What is the equation for total entropy change?

A
36
Q
A
37
Q

What is the equation for Gibbs free energy?

A
38
Q

How does gibbs free energy tell if a reaction is feasible at that temperature?

A

If gibbs is 0 or -ve, reaction is feasible.

39
Q

Why might a reaction not be observed even though it is feasible?

A

The reaction might have high activation energy and/or a slow rate of reaction.

40
Q

Is a reaction feasible if it has a -ve enthalpy change and a +ve entropy change?

A

Yes. It is feasible at any temperature. Gibb’s free energy is -ve at any temperature.

41
Q

Is a reaction feasible if it has a +ve enthalpy change and a -ve entropy change?

A

Never feasible. Gibb’s energy will always be positive

42
Q

Is a reaction feasible if it has a -ve enthalpy change and a -ve entropy change?

A

Only at lower temperatures. Gibb’s free energy will only be negative in lower temperatures.

43
Q

Is a reaction feasible if it has a +ve enthalpy change and a +ve entropy change?

A

Only at higher temperatures. Gibb’s free energy is will only be -ve at higher temperatures.

44
Q

How do you calculate the temperature at which a reaction becomes just feasible?

A
45
Q

What are the values for Kc for reactions with a -ve change in gibbs free energy?

A

Kc is large (greater than 1) because reaction feasible.

46
Q

What are the values for Kc for reactions with a +ve change in gibbs free energy?

A

Kc is less than 1. The reaction isn’t feasible.

47
Q

What is the equation linking gibb’s free energy and Kc?

A