Enthalpy changes Flashcards

1
Q

Enthalpy H ;

A

heat content of system

@ constant pressure

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2
Q

Enthalpy change ∆H°;

A

heat added to a system

@ constant pressure

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3
Q

Enthalpy change ∆H EQ

A

(∆H = H products - H reactants)

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4
Q

Exothermic energy profile

A

Reactants > Products

= -ve

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5
Q

Endothermic energy profile

A

Products> Reactants

= +ve

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6
Q

Conservation of energy;

A

energy cannot be

destroyed

created

only changed from one form to another

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7
Q

Standard Conditions

A
  • All substances = standard states
  • 298k
  • 1 atm
  • conc - 1mol-1dm3
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8
Q

Standard enthalpy of formation;

A

One mole of substance is formed from constituent elements in standard states under standard conditions

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9
Q

Standard enthalpy of combustion

A

One mole of substance is completely burned/ combusted in O2 under standard conditions

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10
Q

Standard state used should be………….

A

Elements that are most stable at 298k, 1 atm

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11
Q

Enthalpy change of reaction

A

change in a reaction between number of moles of reactants shown in the equation form the reaction

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12
Q

Hess’s Law

A

total enthalpy change for reaction

independent of route taken from reactants to products

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13
Q

Hess’s law general EQ

A

ΔH1= ΔH2 + ΔH3

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14
Q

H.L Combustion

A

Arrows point down

ΔcH = Reactants - Products

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15
Q

H.L Formation

A

Arrows point up

ΔfH = Products - Reactants

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16
Q

Bond enthalpy;

A

Enthalpy required break covalent X-Y

into atoms X and Y

all in the gas phase

17
Q

Average bond enthalpy;

A

average value of enthalpy

required to break given type of covalent bond

gaseous species

18
Q

Breaking bonds = …………….

A

endothermic - req energy

19
Q

Making bonds = ……………..

A

exothermic - releases energy

20
Q

Calorimeter;

A

Vessel determination of heat/ temp changes over time

21
Q

Measuring enthalpy changes expression

A

q = mcΔT

mass refers to mass of water ; 100cm of water heated = 100g

c = 4.18Jg-1k-1

Always remember to convert answer to kJ by dividing by 1000

22
Q

Calculating moles

A

n = m/M

n= c x v (always remember to change volume into dm-3)

23
Q

ΔH = ……….

A

ΔH = -q/n

Units = kJmol-1

24
Q

Determining enthalpy of combustion - Prac

Possible improvements………. 1,2,3

A
  1. Graph - extrapolating - reduces the error caused by heat loss to surroundings
  2. Draught shield/ screen - maximise heat transfer from flame to water
  3. Water - stirred continually - ensure even temp
25
Q

ΔH combustion = always lower than the book

Why?

A
  • Energy transferred from burning alcohol = lost to surroundings + apparatus
  • Alcohol not completely combusted = soot at bottom of calorimeter - indicator
26
Q

To determine more accurate enthalpy changes a ……….. can be used

Better - why?

A

bomb calorimeter

  1. Stirrer - uniform temp
  2. Insulation
  3. Lid
  4. ………………………
27
Q

Indirect determination of enthalpy change

Coffee cup calorimeter

What?

A
  • Changes that take place in aq
  • Sealed + insulated container
  • Temperature noted at regular intervals over a period of time
28
Q

Why use polystyrene cup?

How could it be improved further?

A
  • Insulates - heat lost or absorbed = negligible

Improved by

  1. Placed inside another polystyrene cup
  2. Beaker lagged with cotton wool

= Improved insulation

29
Q

ΔH = found using calorimetry = never completely accurate

Why?

A
  • Energy easily lost through conduction or convection
  • Inaccuracies measuring temperature
30
Q

Ex Calorimeter Experiment

A

Magnesium oxide + Acid (HCl)

Magnesium carbonate + Acid (HCl)