Energetics Flashcards

1
Q

Exothermic Processes

A

Energy is released from the chemical to the surroundings during the process
The temperature of the surroundings increases
ΔH is negative

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2
Q

Endothermic Processes

A

Energy is taken in by the chemical from the surroundings during the process
The temperature of the surroundings decreases
ΔH is positive

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3
Q

Enthalpy Changes definiton

A

heat energy change at constant pressure (kJ mol-1)

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4
Q

Standard Conditions

A
  • 100 kPa pressure
  • 298 K temperature
  • 1.0 mol dm^3 concentration
  • When an enthalpy change is measured under standard conditions it is written as ΔHθ.
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5
Q

Enthalpy level diagrams

A

Breaking bonds requires energy and is an endothermic process

Making bonds releases energy and is an exothermic process

*need initial input of energy- Ea

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6
Q

Ea definiton

A

Activation Energy, Ea, is the minimum needed energy to start a reaction

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7
Q

Mean bond enthalpy definition

A

heat energy required to break one mole of a covalent bond into gaseous atoms, averaged over a range of different compounds

E.g. O2(g) → 2O(g)

  • always endothermic
  • more positive bond enthalpy, larger the amount of energy needed to break bond= stronger bond
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8
Q

Standard enthalpy of formation

A

The enthalpy change when one mole of substance is formed from its constituent elements under standard conditions with all reactants and products being in their standard states.

e.g. H2(g) + ½O2(g) → H2O(l)

-ΔHf of all elements in standard state = 0

-why would reaction not show ΔHf - forms two moles not one

Hess cycle = ↑

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9
Q

Standard enthalpy of combustion

A

The enthalpy change when one mole of a substance is completely burnt in excess oxygen under standard conditions, all reactants and products being in their standard states

e.g. CH4(g) + 2O2(g)  CO2(g) + 2H2O(g)

  • Substances that cannot be combusted like water, carbon dioxide and most other oxides, have zero enthalpy of combustion
  • always exo, always negative
  • difficult to measure = incomplete combustion

Hess cycle = ↓

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10
Q

Enthalpy of Reaction

A

any reaction that does not match any of the above

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11
Q

Hess’ Law definition

A

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

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12
Q

Bond enthalpy Calculation

A

BERP

reactants - products

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13
Q

Oxygen bond

A

O2 only substance with O=O bond

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14
Q

Why is databook value different

A

databook derived from different compounds

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15
Q

calorimetry equations

A

Q=mcΔT (Q/1000)
ΔH=Q/n

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16
Q

Combustion calorimetry

A

Temp of water ↑ = exo, -ΔH
Temp water ↓ - endo, +ΔH

use mass of water

17
Q

Calorimetry with two solutions reacting

A
  • use total solution vol when calculating mass
  • use moles of limiting factor - lower mol
18
Q

Calorimetry- adding solid to solution

A
  • only use mass of water
  • don’t use excess moles
19
Q

Assumptions made in calorimetry

A

energy transferred from reacting chemicals is equal to energy released by reaction

20
Q

Combustion Calorimetry Sources of error

A
  • Heat loss to the surroundings
  • Incomplete combustion of the fuel
  • Heat energy transferred to the metal calorimeter
  • Some fuel evaporates

Improvements to Minimise Sources of Error
* Add a lid – reduces heat loss
* Insulate sides of calorimeter – reduces heat loss
* Reduce distance between flame and beaker – reduces heat loss
* Put sleeve around flame to protect it from draughts

21
Q

Solution Calorimetry Sources of error

A
  • Heat loss to the surroundings

Improvements to Minimise Sources of Error
* Add a lid – reduces heat loss
* Insulate calorimeter – reduces heat loss

HEAT LOSS BIGGER ISSUE THAN UNCERTAINTY

22
Q

Enthalpy Change Using a Cooling Curve

A

1)
-measure water with measuring cylinder (100cm3)
-into polystyrene cup
-add known mass of MgCl

2)
-record initial temp until constant
-min 5 solid added
- record temp at regular intervals
-cooling till trend established

3)
Q=mcΔT
ΔH=Q/n