topic 8: energetics 1 Flashcards

1
Q

enthalpy change defintion

A

heat energy change measured at constant pressure

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2
Q

standard conditions

A
  • 100 kPa
  • 298 K
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3
Q

exothermic delta h

A

negative

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4
Q

endothermic delta h

A

positive

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5
Q

standard enthalpy change of formation defintion

A

-enthalpy change when 1 mole of the compound
-is formed from its elements under standard conditions
- under standard conditions 100 kPa and 298 K
e.g Mg(s) + Cl2(g) -> MgCl2(s)

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6
Q

enthalpy of formation of an element

A

0

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7
Q

standard enthalpy change of combustion

A

-enthalpy change when 1 mole of a substance is completely combusted in oxygen
-under standard conditions 100 kPa and 298 K

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8
Q

compare exothermicity of incomplete vs compete combustion

A

incomplete is LESS EXOTHERMIC than complete

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9
Q

enthakpy change of reaction defintion

A

enthalpy change when the number of moles of reactants as specified in the balanced equation react together

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10
Q

enthalpy change of neutralisation defintion

A

enthalpy change when acid and alkali react togetehru nder standard conditions to produce 1 mole of water

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11
Q

enthalpy changes of neutralisation are …

A

EXOTHERMIC

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12
Q

equation for energy transferred (Joules)

A

Q = m * c* delta T

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13
Q

in calrometry, state effect if you: double volume of excess solution

A

no effect

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14
Q

in calrometry, state effect if you: do the experiment in a glass beaker

A
  • heat loss to surroundings
  • smaller delta T
  • delta h is LESS EXOTHERMIC
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15
Q

in calrometry, state effect if you: USE LARGE CHUNKS OF SOLID

A
  • slower reaction rate so more time for heat loss to surroundings
  • q smaller
  • delta h less exothermic
    TO IMPROVE USE AN EXTRAPOLATION CURVE
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15
Q

in calrometry, state effect if you: double mass of solid

A
  • q is doubled
  • n is double
  • no effect on delta h
16
Q

in calrometry, state effect if you: initial temperature of solution is higher

A
  • more heat loss at a faster rate
  • smaller delta t, q, delta H
17
Q

in calrometry, state effect if you: use more concentrated solution but in excess

A
  • no effect
18
Q

in calrometry, state effect if you: use a fine powder

A
  • larger SA
  • faster rate of reaction so less heat loss
  • larger values
19
Q

largest source of error in calorimetry and how to fix?

A
  • heat loss to surroundings
  • do a temperature correction curve w/ extrapolation
20
Q

why not use a larger volume of acid in calorimetry is its in excess

A
  • already in excess so NO NEED
  • temperature change becomes smaller , so higher percentage error
21
Q

mean bond enthalpy

A

enthalpy needed to break the covalent bond in gaseous atoms, averaged over different molecules

22
Q

bond enthalpies are always …

A

POSITIVE
- as bond breaking is endothermic

23
Q

problem with mean bond enthalpies

A
  • average so not for specific bond
  • assumed for GAS, if a liquid or solid more energy required to change state
24
Q

why is experimental values of bond enthalpy less acurate?

A
  • heat loss to surroundings
  • incomplete combustion so less energy released
25
Q

why use a hess cycle?

A
  • hard to measure temperature of a solid
  • FOR ENDO: hard to add heat and measure temperature change at the same time
26
Q

mass in calrometry

A
  • mass of SOLUTIONS
  • for combustion, mass of WATER
27
Q

MEAN BOND ENTHALPY

A

reactants - products

28
Q

error calrometry COMBUSTION

A
  • heat loss to surroundings
  • EVAPORATION OF SOLUTIOM
  • incomplete combustion
  • specific heat capacity of apparatus ignored
29
Q

delta H from BONDS

A

reactants minus products

30
Q

delta H from anything bUT bonds

A

products minus reactants

31
Q

effect of smoky flame on experimental combustio value

A
  • incomplete combustion
  • value is LESS EXOTHERMIC