C9-10. Enthalpy Changes Flashcards

1
Q

How do we define enthalpy?

A

Enthalpy is a measure of the energy stored in a system.

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2
Q

How can we observe enthalpy change?

A
  • Enthalpy changes occur when energy is given out or taken into account system during reaction. It cannot be directly measured.
  • We observe it as a temperature change, using a thermometer or temperature probe.
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3
Q

How can we calculate enthalpy change?

A
  • We use Q=mcT to find the total energy change in the system.
  • This is then converted to kJ, before being divided by the number of moles of the subject of the calculation to calculate delta-H.
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4
Q

What are the standard conditions for measuring enthalpy changes?

A
  • 100 kPa
  • 298 K
  • 1 mol dm-3
  • Standard states of all reactants and products
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5
Q

Define standard enthalpy change of combustion.

A

The enthalpy change when 1 mole of a substance undergoes complete combustion under standard conditions.

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6
Q

Define standard enthalpy change of reaction.

A

The enthalpy change of a reaction in the molar quantities shown in the chemical formula under standard conditions.

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7
Q

Define standard enthalpy change of formation.

A

The enthalpy change when 1 mole of a substance is formed from its constituent elements under standard conditions.

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8
Q

Define standard enthalpy change of neutralisation.

A

The enthalpy change when 1 mole of water is produced during a reaction between an acid and base under standard conditions.

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9
Q

What is an exothermic reaction?

A

Exothermic reactions occur when the products formed have less energy than the reactants used, since energy is transferred to the surroundings.

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10
Q

What is an endothermic reaction?

A

Exothermic reactions occur when the products formed have greater energy than the reactants used, since energy is transferred from the surroundings.

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11
Q

How do we use cooling curves?

A
  • Plot 2 lines of best fit: one for the starting temperature, and one for the temperature change.
  • Extrapolate the latter to the time at which the reaction was initiated.
  • Find the difference between this point and the initial temperature.
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12
Q

How can we practically measure enthalpy changes?

A
  • We use an insulated reaction vessel containing reacting substances and a thermometer.
  • We record temperature every minute until it is stable, before initiating the reaction and continuing to record temperature.
  • We then use cooling curves to determine max. delta-H.
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13
Q

Why do we need to use cooling curves?

A

They allow us to estimate the enthalpy change at the instant of the reaction, at which point negligible energy has been lost to the surroundings.

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14
Q

What sources of error do cooling curves let us account for?

A
  • Evaporation of the reacting substance
  • Loss of thermal energy to the surroundings
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15
Q

What can often affect measured/estimated enthalpy change?

A
  • Evaporation of reacting substances
  • Loss of thermal energy to the surroundings through lack of insulation
  • Other reactions occurring with different enthalpies such as incomplete combustion
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16
Q

What is the activation energy of a reaction?

A

The minimum energy required to enable to a reaction to take place. This is attained when the energy input is sufficient to break the bonds in the reactants.

17
Q

Is bond breaking exo- or endo-thermic?

A

Energy is required to break bonds, therefore bond breaking is an endothermic process.

18
Q

Is bond formation exo- or endo-thermic?

A

Energy is released when bonds are formed, therefore bond formation is an exothermic process.

19
Q

How can we use bond enthalpies to estimate enthalpy change?

A

(sum of bonds broken) - (sum of bonds formed) = enthalpy change.

20
Q

Why is the use of bond enthalpies of calculate enthalpy change only an estimation?

A
  • The values we are provided are average bond enthalpies.
  • These are an average value taking into account the enthalpy changes of the bond in all molecules involving the named bond.
  • These vary between molecules.
21
Q

Why is it difficult for us to measure enthalpies accurately or easily?

A
  • The activation energy may be high.
  • The reaction rate may be very slow.
  • Multiple reactions could be occurring at once, especially during the formation of hydrocarbons.
22
Q

Summarise Hess’ law.

A
  • This states that the overall enthalpy change for a reaction is independent of the route taken, in a closed system.
  • I.e. the enthalpy change of the direct route X>Y equals that of the indirect route X>Z>Y.
23
Q

How can we use Hess cycles to determine overall enthalpy changes using enthalpy change of formation?

A
  • Using formation, overall enthalpy change of X>Y would equal that of (Z>Y) - (X>Z).
  • We know this because the arrows we draw point upwards from the elements.
24
Q

How can we use Hess cycles to determine overall enthalpy changes using enthalpy change of combustion?

A
  • Using combustion, overall enthalpy change of X>Y would equal that of (X>Z) - (Z>Y).
  • We know this because the arrows we draw point downwards towards the elements.
25
Q

How do we use Hess’ law to calculate overall enthalpy change for a reaction?

A
  • If we are given known enthalpy changes of combustion/formation of an indirect reaction pathway, we can combine these algebraically to produce an overall enthalpy change.
  • For enthalpy of formation: (Z>Y) - (X>Z) = (X>Y)
  • For enthalpy of combustion: (X>Z) - (Z>Y) = (X>Y)
26
Q

What happens to the temperature of the surrounding in…
- exothermic reactions
- endothermic reactions

A
  • Temperature increases. Energy is transferred to the surroundings from the system.
  • Temperature decreases. Energy is transferred from the surroundings to the system.
27
Q

Why do reactions involving small activation energies often take place very readily?

A

The energy required to surpass this activation energy and break bonds is readily available from the surroundings alone.

28
Q

What is the standard enthalpy change of formation of an element from itself?

A

This is always 0 kJ mol-1, since no change occurs when forming one mole of an element from itself. This is important in Hess cycles, where this idea comes up regularly.

29
Q

What state do all species need to be in when determining enthalpy changes from average bond enthalpies? Why is this?

A

All species must be in the gaseous state. This is because average bond enthalpy is the energy required to break one mole of a specific bond in a gaseous molecule.

30
Q

Define specific heat capacity.

A
  • This is the energy required to raise the temperature of 1g of a substance by 1 K.
  • Note that this differs from the definition of SHC in Physics.
  • SHC is given by the letter c.
31
Q

What assumptions can we make when completing calorimetry calculations?

A
  • We can assume that the density of water in a calorimeter is 1 g cm-3.
  • We can also assume that the specific heat capacity of water in a calorimeter is 4.18 J g-1 K-1.