enthalpy changes: content Flashcards

(23 cards)

1
Q

exothermic reactions

A

the products are at a lower energy than the reactants: excess heat is transferred from the system to the surroundings
ΔH is negative

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2
Q

endothermic reactions

A

products are at a higher energy than the reactants: heat is taken in from the surroundings to the system
ΔH is positive

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3
Q

enthalpy profile diagrams

A
  • gaseous atoms
  • reactants
  • products
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4
Q

standard conditions [ ]ᶿ

A

298K
100kPa
1.00moldm⁻³

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5
Q

standard enthalpy change of formation for an element

A

zero (by definition)

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6
Q

examples of exothermic reactions

A

combustion
respiration
neutralisation

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7
Q

examples of endothermic reactions

A

thermal decomposition
evaporation
photosynthesis

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8
Q

what are the two calorimetry equations

A

q=mcΔT
q - energy change (J)
m - mass of solution/surroundings (g)
c - specific heat capacity of solution/surroundings (J kg⁻¹ K⁻¹)
ΔT - temperature of solution/surroundings (K)

ΔH=±q/n
ΔH - enthalpy change (kJ mol⁻¹)
q - enthalpy change (kJ)
n - moles of reactant/system (mol)

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9
Q

methods to determine enthalpy changes

A

combustion calorimetry
calorimetry with a reaction in solution

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10
Q

combustion calorimetry overview

A

a known mass of substance/fuel is burned to heat a known mass of water

system- fuel burning
surroundings- water

ALWAYS exothermic - ΔH is negative

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11
Q

sources of error in combustion calorimetry

A
  • heat lost to the air
  • incomplete fuel combustion
    [evaporation of fuel/water from wick/beaker]
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12
Q

how to minimise error in combustion calorimetry

A
  • ensure a plentiful oxygen supply (in excess)
  • add a lid to the beaker
  • use a copper can instead of a beaker (better conductor)
  • cover wick when not burning
  • use an insulated/bomb calorimeter
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13
Q

calorimetry with a reaction in solution overview

A

a known quality of reactant (limiting!!) reacts in a known volume of water

system- the chemicals reacting or dissolving
surroundings- the solution

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14
Q

sources of error in reaction in solution calorimetry

A
  • heat loss/gain to/from the air
  • water evaporates from the beaker
  • incomplete reaction
  • c of solution ≠ c of water
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15
Q

how to minimise error in reaction in solution calorimetry

A
  • use a polystyreine cup
  • use a lid to prevent heat loss/gain
  • ensure standard conditions
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16
Q

bond enthalpies are always _____

A

endothermic (positive ΔH values)

17
Q

bond breaking is

A

endothermic
(=activation energy)

18
Q

bond making is

19
Q

how to calculate ΔH

A
  • draw out the equation
  • calculate totals for bonds made/broken
  • use the equation to calculate overall enthalpy changes
  • [sketch reaction profile]
20
Q

why can reactions be exothermic

A

more energy is released (forming bonds in the products) than is required (breaking bonds in the reactants)

21
Q

why might it not be possible to directly measure enthalpy changes from experiments

A
  • very high activation energy Eₐ
  • very slow rate of reaction
  • occurrence of side reactions
22
Q

how to indirectly calculate enthalpy changes

A

hess’ law: the enthalpy change for a given reaction is independant of the route taken
draw an enthalpy cycle (kinda like vectors)
BE CAREFUL of the enthalpy change direction

23
Q

required practical: enthalpy determination

A
  • pour the aqueous reactant into a polystyreine cup and cover
  • use a thermometer to record the temperature every minute for three minutes to get an accurate start temperature
  • add the other reactant and stir to ensure a homogenous mixture
  • record the temperature after one minute
  • continue to record the temperature at one minute intervals
  • calculate ΔT
  • plot ΔT against time
  • extrapolate two lines of best fit
  • read ΔT at the point of mixing