Energetics Flashcards

1
Q

define standard enthalpy of combustion

A

enthalpy change when one mole of a substance is burned completely in oxygen under standard conditions, all substances in their standard state
under standard conditions

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2
Q

molar enthalpy change equations:

A
  • q (heat energy / J) = mc^T
  • ^H (kJ mol) = q (kJ) / n (limiting reactant)
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3
Q

what is molar enthalpy change △H?

A

The amount of heat energy absorbed or released for every mole of the substance which reacts

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4
Q

reactivity and enthalpy of C-X (halogenoalkane) relationship

A

if less energy require to break C-X bond, molecule will react faster and more readily as activation energy will be lower

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5
Q

how would the boiling points vary between an alkane and a halogenoalkane of the same Mr

A
  • Halogenoalkanes have higher b.p.
  • C- X bond is polar ➜ halogenoalkane forms PDD interactions and VdW forces between molecules the alkanes only form VdW forces between molecules
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6
Q

How does the boiling point change of a halogenoalkane down the group

A

larger Mr -> Increased VdW forces between molecules
* Even though the polarity of the C-X bond decreases, so weaker PDD interaction,
* HOWEVER, higher Mr means stronger VdW forces, which outweighs the PDD interaction

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7
Q

Suggest one reason, other than incomplete combustion or heat transfer to the atmosphere, why the student’s value for the enthalpy of combustion of methanol is different from that in a Data Book.

A

Experiment not done under standard conditions

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8
Q

The student said correctly that using a thermometer with an overall uncertainty for the rise in temperature of ±0.5 °C was adequate for this experiment. Explain why this thermometer was adequate for this experiment.

A

Temperature rise is significantly bigger than uncertainty.

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9
Q

Suggest one improvement that would reduce errors due to heat loss in the student’s experiment.
(1 Mark)

A

Reduce the distance between the flame and the beaker

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10
Q

what is bond enthalpy

A

energy required to break or form a bond

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11
Q

Standard conditions are:

A
  • 298 K (25°C)
  • a pressure of 1 bar (100 kPa).
  • where solutions are involved, a concentration of 1 mol dm-3
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12
Q

When calculation mean bond enthalpies ALWAYS remember:

A

the C-C / C=C bonds

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13
Q

Definition: Enthalpy change

A

Enthalpy change is the amount of heat energy transferred out during any change in a system provided the pressure is constant.

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14
Q

suggest how the students method and analysis of results could be improved: (6)

A
  • a polystyrene cup could be used with an insulating lid
  • to reduce heat loss
  • temp readings recorded every 30 sec for 3 minutes before addition of solid to measure accurate starting temp
  • regular temp readings after adding every 30 sec
  • graph of temp v time plotted, extrapolating two lines of best fit to gain max temp change
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15
Q

Suggest one reason, other than the use of mean bond enthalpies, why a value for the enthalpy of combustion of a liquid alkane is different from the value obtained using the expression for enthalpy of combustion: (1)

A
  • (enthalpy of combustion) equation only relates to gaseous alkanes (by definition)
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16
Q

Hess’ Law

A

enthalpy change is independent of the route taken

17
Q

Describe thermal cracking:

A
  • high temperature (500C)
  • high pressure (7000 kPa)
  • produces mostly alkenes, (+some H2 for haber process)
18
Q

Describe catalytic cracking:

A
  • moderate pressure
  • high temp (450C)
  • zeolite catalyst
  • prod. branched and cyclic alkanes and aromatic HC’s
  • used for making motor fuels