CL 9- enthalpy Flashcards

1
Q

activation energy

definition

A

the minimum energy required for a reaction to take place

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2
Q

standard conditions

A

pressure of 100kPa, temperature of 298K, and a concentration of 1moldm⁻³

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3
Q

standard states

definition

A

the physical state of a substance under standard conditions

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4
Q

standard enthalpy change of reaction

definition

A

the enthalpy change that accompanies a reaction in the molar quantities shown in a chemical equation, under standard conditions, with all reactants and products in their standard states

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5
Q

standard enthalpy change of formation

definition

A

the enthalpy change that takes place when 1 mole of a compound is formed from it’s elements, under standard conditions, with all reactants and products in their standard states

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6
Q

standard enthalpy change of combustion

definition

A

the enthalpy change that takes place when 1 mole of a substance completely reacts with oxygen, under standard conditions, with all reactants and products in their standard states

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7
Q

standard enthalpy change of neutralisation

definition

A

the enthalpy change that accompanies the reaction of an acid by a base to form 1 mole of water, under standard conditions, with all reactants and products in their standard states

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8
Q

equation for ΔH

A

Q=mcΔT
enthalpy change=mass x SHC x change in temp

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9
Q

average bond enthalpy

definition

A

the energy required to break 1 mole of a specified type of bond in a gaseous molecule

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10
Q

why are bond enthalpies always positive?

A

they are endothermic- energy is required to break a bond

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11
Q

in terms of bonds breaking/making

explain an exothermic reaction

A

energy released when making bonds in the products is greater than the energy required to break the bonds in the reactants

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12
Q

in terms of bonds breaking/making

explain an endothermic reaction

A

the energy required to break the bonds in the reactants is greater than the energy released when new bonds are made in the products

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13
Q

enthalpy change of neutralisation method

A
  • measure 25cm³ of acid and 25cm³ of alkali in separate measuring cylinders
  • set up a polystyrene cup in a beaker (to keep it upright) and a thermometer, and add the acid
  • record the inital temperature, and then continue to record temp every 30 seconds
  • at the 3 minute mark, add alkali and record temp
  • continue recording temp every 30 seconds until you reach 10 minutes, or reach a final max temp
  • calculate energy exchanged with Q=mcΔT
    enthalpy change is negative
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14
Q

enthalpy change of combustion method

A
  • measure 100cm³ of water with a measuring cylinder and pour into calorimeter
  • take an initial reading of the water temperature with a thermometer
  • weigh the spirit burner with ethanol and the lid on, and record the mass
  • place spirit burner underneath calorimeter and light the wick (don’t move spirit burner once it’s been lit)
  • stir the water with a glass rod
  • when water reaches 70°C, put out the flame by placing the lid back on the spirit burner with tongs
  • measure the mass of the spirit burner, lid and ethanol
    difference in masses= mass of alcohol used in reaction(used to calculate moles)
  • use Q=mcΔT to determine the enthalpy change
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15
Q

sources of error for enthalpy change of combustion

A
  • heat loss to the surroundings from spirit burner, wick and calorimeter
  • evaporation of water
  • evaporation of alcohol
  • incomplete combustion of alcohol
  • reaction is unlikely to occur under standard conditions
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16
Q

improvements to enthalpy change of combustion practical

to avoid sources of error

A
  • improving draught exclusion by adding a draught shield
  • minimising the distance between the flame and the calorimeter
  • placing a cap on the calorimeter
  • insulating the spirit burner and calorimeter
17
Q

how to reduce percentage error

A
  • use a piece of apparatus with a higher resolution
  • use the same equipment but with larger quantities
18
Q

hess’s law

A

if a reaction can take place by more than one route, the total enthalpy change is always the same, no matter which route is taken

19
Q

which way do the arrows point for combustion?

hess’s law cycle

A

down

20
Q

which way do the arrows point for formation?

hess’s law cycle

A

up