1.4 Energetics Flashcards Preview

AQA A-Level Physical Chemistry > 1.4 Energetics > Flashcards

Flashcards in 1.4 Energetics Deck (36)
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1
Q

What is enthalpy change?

A

Heat energy change at a constant pressure

2
Q

How does a thermometer in a hot substance?

A

It absorbs heat energy from the liquid so the particles gain more kinetic energy and move apart
The space between the particles increases and the substance therefore becomes less dense
The particles will therefore rise showing a temperature increases

3
Q

How does a thermometer work in a cool substance?

A

Little to no heat supplied means the particles lose kinetic energy and move closer together
The energy moves out of the thermometer and into the substance
The space decreases between the particles and become more dense
The particles will then sink showing a decrease in temperature

4
Q

What are the two systems in a chemical reaction?

A

Chemical system - reactants and products only

Surrounding system - everything! Hand, beaker, atmosphere, thermometer etc…

5
Q

What does a thermometer record?

A

The temperature of the surroundings

6
Q

What is the endothermic part of a reaction?

A

Where bonds are broken

The activation energy

7
Q

What is an endothermic reaction?

Examples?

A

Reactions which take in heat energy from the surroundings as the reaction takes place

Results in a positive delta H ie increase in enthalpy change

Photosynthesis

8
Q

What does an endothermic reaction result in?

A

A decrease in temperature surroundings

11
Q

What is an exothermic reaction? Examples?

A

Reactions in which heat energy is released to the surroundings as the reaction takes place

Results in a negative delta H ie decrease in enthalpy change

Respiration and Combustion

12
Q

What are the standard enthalpy change symbols?

A

H - enthalpy
Δ - change
θ - standard

ΔH ^θ

13
Q

What are standard conditions?

A

Temperature - 298k

Pressure - 100kPa

14
Q

What is standard enthalpy change? ΔH ^θ

A

Heat energy change at a constant pressure and under standard conditions

15
Q

What is standard enthalpy of reaction? ΔH ^θr

A

The enthalpy change for a chemical reaction under standard conditions and all substances in their standard states

16
Q

What is standard molar enthalpy of combustion? ΔH ^θc

A

The enthalpy change that takes place when 1 mole of a substance completely reacts with excess oxygen under standard conditions and all reactants and products being in their standard state

17
Q

What is standard molar enthalpy of formation? ΔH ^θf

A

The enthalpy change that takes place when 1 mole of a substance is formed from its constituent elements under standard conditions with all reactants and products in their standard states

18
Q

What does an exothermic reaction result in?

A

An increase in temperature surroundings

19
Q

What is the exothermic part of a reaction?

A

Bond making - to produce products

20
Q

What are mean bond enthalpies?

A

The average energy change required to break 1 mole of a particular covalent bond with all species in the gaseous state averaged over many different molecules

21
Q

What are bond enthalpies?

A

The energy change required to break 1 mole of a particular covalent bond with all species in the gaseous state

22
Q

What is the equation to work out (mean) bond enthalpies?

A

ΔH = ∑ (mean) bond enthalpies of reactants - ∑ (mean) bond enthalpies of products

23
Q

What is Hess’ law?

A

The enthalpy change for a reaction is independent of the reaction pathway taken as long as the starting and ending reaction conditions are the same

24
Q

Give a general summary of a Hess cycle?

A

The enthalpy change for a chemical reaction is the same whatever route is taken from reactants to products

ΔH1 = ΔH2 + ΔH3 (as ΔH1 may be too difficult to work out)

25
Q

When working out enthalpy changes what must we do?

A

Look at the DATA provided!!!
To determine the equation

(Not the balanced equation)

26
Q

What equation is used for working out enthalpy of formation?

Using COMBUSTION DATA?

A

ΔH^θf =

∑ ΔH^θc reactants - ∑ ΔH^θc products

27
Q

What equation is used for working out enthalpy of combustion?

Using FORMATION DATA?

A

ΔH^θc =

∑ ΔH^θf products - ∑ ΔH^θf reactants

28
Q

Points about constructing Hess cycles?

A
  • All arrows go away from elements
  • If elements are reactants ‘magical oxygen’ is used to make compounds
  • If reactants are compounds it will go back to its elements for ‘underneath’ reaction
  • if large product on right arrow will go to many products underneath
29
Q

What to remember in combustion reactions?

A

Oxygen is a reactant

30
Q

What are the parts of an enthalpy level diagram?

A

Enthalpy in KJ up the side
Time in seconds (s) across the bottom
Activation energy
Overall enthalpy change KJ mol^-1 (+ or -)

31
Q

What is the calorimetry calculation?

A

q = mc ΔT

q = heat enthalpy (J)
m = mass of water (ml)
c = specific heat capacity 
ΔT = temperature change (degrees C)
32
Q

What is important to remember about q (heat enthalpy)

A

You have to put (+ or -) depending on if it was exothermic or endothermic

Look at the ΔT to work out

33
Q

What is standard enthalpy of neutralisation?

A

The enthalpy change that accompanies the formation of one mole of water from an acid-base/alkaline reaction with all reactants and products in their standard states and under standard conditions

34
Q

What are some issues with ‘coffee cup’ calorimetry?

A

Heat loss
Incomplete reaction
Not in standard conditions

35
Q

What are some advantages of a bomb calorimeter over a combustion calorimeter?

A

Well insulated
Pure oxygen = complete combustion

Leads to very accurate combustion values fr food packets

36
Q

How to calculate ΔT from a graph?

A

Draw a vertical line up where the reaction started
Draw a line of best fit from the high values to your vertical line (no anomalies) (can be straight or curved)
Draw a line of best fit from the low values to your vertical line

Where your lines of best fit hit the vertical line - ΔT is the difference between those values

37
Q

If you have to draw a graph to determine ΔT, what features would it have?

A

Temperature up the side
Time across the bottom
Often broken axis as temp doesn’t need to start at zero

Vertical line where the reaction starts

38
Q

What do you have to in molar enthalpy of neutralisation calculations?

A

q = mc ΔT

Then work out the moles (usually from concentration and volume)
Ratio to get the Joules to 1 mole

Convert to KJmol^-1