Energetics Flashcards

(31 cards)

1
Q

Define enthalpy change (ΔH)

A

Enthalpy change is the heat energy transferred during a chemical reaction at constant pressure.

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2
Q

State the units of enthalpy change.

A

kJ mol⁻¹
J= kJ /1000

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3
Q

What are the standard conditions for measuring standard enthalpy changes (ΔH°)?

A

298 K (25°C), 100 kPa, and substances in their standard states.

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4
Q

Give the correct notations for the following types of standard enthalpy changes: a) Reaction b) Combustion c) Formation

A

a) Δ Н°r
b) Δ Н°С
c) Δ H°f

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5
Q

What happens in an exothermic reaction?

A

In an exothermic reaction energy is released and the temperature increases

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6
Q

What is the ΔH sign of an exothermic reaction? And give an example of an exothermic reaction

A

Negative (-)
An example of an exothermic reaction is Combustion

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7
Q

What happens during an endothermic reaction?

A

In an endothermic reaction Energy is absorbed and temperature decreases

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8
Q

What is the ΔH sign if an endothermic reaction? State an example of an endothermic reaction

A

Positive (+)
An example of an endothermic reaction is Photosynthesis

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9
Q

Bond Enthalpies

Define bond enthalpy

A

Bond enthalpy is the energy required to break one mole of bonds in gaseous molecules.

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10
Q

Is breaking bonds exothermic or endothermic? State the sign of ΔH.

A

Breaking bonds is endothermic; ΔH is positive (+).

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11
Q

Is forming bonds exothermic or endothermic? State the sign of ΔH.

A

Forming bonds is exothermic; ΔH is negative (−).

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12
Q

Write the formula for calculating overall enthalpy change using bond enthalpies.

A

ΔH = Bonds broken − Bonds formed

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13
Q

Why do we use mean bond enthalpies?

A

We use mean bond enthalpies because they are averages across compounds from data tables.

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14
Q

Calculating Enthalpy Change from Bonds

List the steps to calculate enthalpy change using bond enthalpies.

A
  1. Draw molecules to count all bonds.
    1. Use bond enthalpy values and multiply by the number of each bond.
    2. Apply: ΔH = Total bonds broken − Total bonds formed
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15
Q

Measuring Enthalpy Changes Experimentally

Why is a polystyrene cup used in solution experiments?

A

To reduce heat loss.

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16
Q

State the equation used to calculate heat energy change. Define all terms.

A

q = mcΔT
Where:
• m = mass of solution (g)
• c = specific heat capacity (4.18 J g⁻¹ K⁻¹)
• ΔT = temperature change (K or °C)

17
Q

Combustion

Describe the steps to determine enthalpy change of combustion using a calorimeter.

A
  1. Burn fuel to heat a known mass of water.
    1. Use q = mcΔT (to find the m= mass of water).
    2. Convert q to kJ.
    3. Find moles of fuel burned: n = mass ÷ Mr
    4. Calculate enthalpy: ΔH = q ÷ n
    5. Remember: ΔH is negative (exothermic).
18
Q

Neutralisation

How do you calculate ΔH for a neutralisation reaction?

A
  1. Use stoichiometry to find moles of water formed.
    1. Calculate q = mcΔT.
    2. Divide q by moles of water to find ΔHneut. ΔH= q/n
19
Q

💧 6. Enthalpy Change of Solution/Dissolution

How is enthalpy change of solution determined experimentally?

A
  1. Add known mass of solute to water and measure temperature change.
    1. Calculate q = mcΔT.
    2. work out moles of solvent by mass/Mr= moles
      4.Find ΔH per mole of solute dissolved. ΔH=q/n
20
Q

Hess’s Law

State Hess’s Law.

A

Hess’s law suggests Total enthalpy change is the same regardless of the route taken.

21
Q

What two types of data can be used in Hess cycles?

A

Enthalpy of combustion values and enthalpy of formation values.

22
Q

Write the equation for Hess’s Law using combustion data.

A

ΔHreaction = ΣΔHc(reactants) − ΣΔHc(products)

23
Q

Write the equation for Hess’s Law using formation data.

A

ΔHreaction = ΣΔHf(products) − ΣΔHf(reactants)

24
Q

What is the ΔHf of elements in their standard states?

25
Practical Sources of Error List common sources of error in enthalpy experiments.
• Heat loss to surroundings • Incomplete combustion • Evaporation of volatile fuels
26
Key equation summery
ΔH = q / n ΔH = Bonds broken − Bonds formed ΔH = ΣΔHf(products) − ΣΔHf(reactants ΔH = ΣΔHc(reactants) − ΣΔHc(products) Energy change (J)
27
What is the standard enthalpy change of reaction (ΔH°r)?
Enthalpy change when a reaction occurs in the molar quantities shown in the chemical equation, under standard conditions. ## Footnote Example: N2(g) + 3H2(g) → 2NH3(g) ΔH°r = -92 kJ mol-1
28
What is the standard enthalpy change of formation (ΔH°f)?
Enthalpy change when 1 mole of a compound forms from elements under standard conditions. ## Footnote Example: C(s) + O2(g) → CO2(g) ΔH°f = -394 kJ mol-1
29
What is the standard enthalpy change of combustion (ΔH°c)?
Enthalpy change when 1 mole of a substance combusts fully in oxygen under standard conditions. ## Footnote Example: CH4(g) + 2O2(g) → CO2(g) + 2H2O(l) ΔH°c = -890 kJ mol-1
30
What is the standard enthalpy change of neutralisation (ΔH°neut)?
Enthalpy change when an acid and alkali neutralise under standard conditions, to form 1 mole of water. ## Footnote Example: HCl(aq) + NaOH(aq) → NaCl(aq) + H2O(g) ΔH°neut = -57 kJ mol-1
31
Explain why values from mean bond enthalpy calculations differ from those determined using hess’s law
• Mean bond enthalpies are not specific to a single molecule. • They are averaged from many compounds/different molecules whereas Hess’s Law use experimental data exact to the compounds, Their physical states and Conditions (298 K, 100 kPa)