Energetics 1 Flashcards

1
Q

standard conditions

A

298K and 100KPa

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2
Q

enthalpy change

A

heat energy change measured at constant

pressure

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3
Q

exothermic

A

when more energy is given out from bonds being formed than is taken in by bonds being broken

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4
Q

endothermic

A

When the breaking of bonds in a reaction requires more energy than is given out by the formation of new bonds

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5
Q

energy diagrams for endo and exo

A
exo= negative, products lower than reactants
endo= positive, products high than reactants
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6
Q

Enthalpy of formation, ∆Hθf

A

The enthalpy change that takes place when mole of substance is formed from its elements in their standard state at a temperature of 298K and pressure of 100kPa

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7
Q

Enthalpy of combustion,∆Hθc

A

The enthalpy change that takes place when mole of substance is completely burned in oxygen at a temperature of 298K and pressure of 100kPa

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8
Q

Enthalpy of neutralisation, ∆Hθc

A

The enthalpy change that takes place when one mole of water is formed in a neutralization reaction at a temperature of 298K and pressure of 100kPa

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9
Q

Enthalpy of reaction, ∆Hθr

A

The enthalpy change that takes place when the number of moles of substances in the equation react at a temperature of 298K and pressure of 100kPa

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10
Q

energy transferred equation

A

mass of water x 4.2 x change in temperature

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11
Q

∆H

A

heat energy/moles

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12
Q

using a calorimeter

A
  1. A measuring cylinder is used to measure out 100cm3 of water.
  2. The water is placed in a calorimeter (basically a metal can).
  3. The liquid to be investigated is placed in a spirit burner. The spirit burner is weighed.
  4. The temperature of the water is noted
  5. The apparatus is set up as shown below.
  6. The liquid is ignited and allowed to heat the water.
  7. After a temperature rise of around 20 oC, the flame is extinguished.
  8. The exact temperature is noted
  9. The burner is weighed to find out how much liquid has been burned.
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13
Q

two main reasons for inaccurate values for enthalpy of combustion

A

Heat loss to the surroundings

Incomplete combustion

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14
Q

Hess’ law

A

For a given chemical change, the overall energy change will always be the same whether the change takes place in one step or a number of steps

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15
Q

combustion Hess at the bottom

A

oxidised elements

arrows going downwards

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16
Q

Formation Hess at the bottom

A

elements

arrows going upwards

17
Q

bond enthalpy

A

∆H when one mole of a bond is broken and reactants and products are gaseous, always endothermic

18
Q

mean bond enthalpy

A

∆H for the breaking of a particular type of bond in a particular molecule, averaged out over all those bonds

19
Q

limits of mean BE

A

bond energies are averages

everything has to be gaseous

20
Q

bond energy

A

broken - made

21
Q

reality of standard enthalpy of combustion

A

exothermic make temp higher than 298K

effects the states of products

22
Q

Reasons enthalpy change of a reaction is different to the data book

A
  • Heat loss/gain to/from surroundings
  • approximation in specific heat capacity of solution
  • neglecting specific heat capacity of calorimeter/apparatus
  • reaction may be incomplete/slow
  • temp change is very small
  • density of solution is taken as the same as water
  • conditions not standard