unit 3 aos 1 Flashcards

sources of energy

1
Q

Endothermic reactions

A

1) absorb thermal energy (gets colder)
2) thermal energy&raquo_space;> chemical energy
3) delta H = positive

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2
Q

Exothermic reactions

A

1) release thermal energy (gets hotter)
2) chemical energy&raquo_space;> thermal energy
3) delta H = negative

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3
Q

Energy profile diagrams

A
  • Vertical axis: enthalpy (kJ/mol or KJ)
  • horizontal axis: progress of reaction
  • exothermic: reactants higher than products
  • endothermic: reactants below products
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4
Q

Complete combustions

A

fuel + 02 (g)&raquo_space;> CO2(g) + H2O(l)

  • product is CO2(g)
  • more oxygen used overall
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5
Q

incomplete combustion

A
  • products: carbon monoxide (CO) or carbon particulates (C)
  • less oxygen used overall
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6
Q

Thermochemical Equations

A

MUST have states and delta H value

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7
Q

FORMULA to convert between mass and moles

A

n = m/M

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8
Q

FORMULA to find energy released by a fuel

A

q = delta H x n
with help from data book

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9
Q

different FORMULAS of delta H

A

1) if in kJ/mol: delta H = q/n
2) if in kJ/g: delta H = q/m
3) if in kJ/mL: delta H = q/v

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10
Q

FORMULA of density

A

d = m/v
- volume can be in both ml & L

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11
Q

FORMULA to find energy absorbed by water

A

q = MCAT

  • given specific heat capacity of water is 4.18 J/g/K
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12
Q

how to find delta H experimentally??

A

1) find temp change of water
- use q = MCAT formula

2) find change of mass of fuel
- use n = m/M

3) then calculate delta H
- use delta H = q/n

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13
Q

FORMULA of percentage efficiency of a ‘fuel’

A

% eff = actual / theoretical x 100
AKA
% eff = output / input x 100

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14
Q

what are systematic errors?

A

links to ACCURACY
(how close a measurement is to the true value)

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15
Q

what are random errors?

A

link to PRECUSION
(how close a measurement is to each other)

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16
Q

WAYS to minimise heat loss (in the experiment)

A

1) add a lid
2) bring flame closer
3) insulate the sides of the beaker
4) place heat shields on sides

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17
Q

stoichiometric ratios

A
  • ALWAYS in moles

unknown / known

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18
Q

what are SLC conditions?

A

temperature @ 25 degrees celsius
pressure @ 100kpa

redox: ph @ 0

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19
Q

universal gas law

A

PV = nRT
- not tested in chem 3/4

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20
Q

FOMULA for volume occupied by gas IN SLC CONDITIONS

A

n = V / Vm

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21
Q

what is the molar volume (Vm) of gases?

A

24.8L/mol

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22
Q

volume to volume stoich:
CONDITIONS + how

A

1) temperature is constant
2) pressure is constant
3) all substances must be gas

  • just multiply ratio with volume
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23
Q

how to find limiting reagent?

A

1) find moles of both reactants
2) divide both by their respective coefficient
3) the lower one = limiting reagent

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24
Q

how to find how much excess reagent is left after all of limiting reagent is used up

A

1) find amount of excess used
2) subtract that value from how much there is left

initial - used

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25
Q

features of a calorimeter

A
  • in 3/4 a SOLUTION calorimeter is tested
  • the sides are insulated to minimise heat loss, so most of the energy goes straight to the water

! heat is transferred directly to water

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26
Q

purpose of stirrer

A

to evenly distribute heat
+
ensure there is a constant temperature

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27
Q

purpose of glass bulb

A

initially separates the reactants and prevents reaction to occur

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28
Q

what is a calorie

A

IT is the energy required to heat up 1g of water by 1 degree celcius

  • there are 4.18 joules in ONE calorie
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29
Q

DEF: calibration factor

A

aka: CF
IT is a measure of how much energy is required to change the temperature of a substance in the calorimeter by 1 degree celcius

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30
Q

FORMULA of calculating the CF

A

CF = energy inputted (E) / the temperature change observed (AT)

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31
Q

DEF: electrical calibration

A
  • when the calorimeter can be calibrated using the electric heater
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32
Q

FORMULA to find the electrical calibration factor CF

A

CF = E / AT

E = VIT
v: voltage (volts(v))
I: current (amps)
T: time (seconds)

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33
Q

DEF: chemical calibration

A
  • the calorimeter can be calibrated chemically by combusting an organic molecule with a known change in enthalpy value
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34
Q

FORMULA for chemical calibration factor CF

A

CF = E / deltaT

E = delta H x n (if in kj/mol)
E = delta H x m (if in kj/grams)

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35
Q

FORMULA of concentration

A

c = n / V

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36
Q

temperature - time graphs

A
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37
Q

what is a renewable fuel? (DEF)

A

a fuel that can be replenished by natural processes within a relativly short period of time.

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38
Q

How is coal formed

A

from the fossilisation of dead? plant and animal matter

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39
Q

crude oil

A
  • non renewable
  • consists of a nixture of hydrocarbons, namely alkanes, ranging from 1 to 30 carbons.
  • carbon is sperated by fractional distilation
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40
Q

WHAT is natural gas

A
  • about 95% CH4 & 5% CO2
  • a gas found underground
  • non-renewable
  • can be found in coal sam gas deposits found in coal mines
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41
Q

WHAT is biogas

A
  • renewable
  • produced from biomass/biowaste
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42
Q

how is biogas produced

A
  • formed from the anerobic breakdown of organic matter by bacteria
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43
Q

Bioethanol

A
  • renewable
  • formed from the fermentation of glucose with the help of yeast
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44
Q

Fermentation equation

A

C6H12O6 (aq) -> 2C2H5OH(aq) + 2CO2

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45
Q

Distillation

A
  • a process of sperating a liquid mixture by boiling the mixture.
  • mixture is heated tp the target temperature
  • that temperature is between two substances boiling points
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46
Q

distillate

A

the substance that is evaporated and condensed back back down in distillation

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47
Q

purpose of distillation

A
  • ## increases efficiency upon combustion of ethanol as less water is present
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48
Q

what biodiesel

A
  • renewable
  • made up of fatty acid methyl ester
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49
Q

biodiesal - formation

A
  • from plant and animal fats/oils
  • transesterification
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50
Q

partially oxidised

A

A fuel that already contains oxygen in the molecular formula (eg. methanol = CH3OH)

THUS HEAT OF COMBUSTION WOULD BE LOWER bc partially oxidised = ‘partially burnt’

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51
Q

Carbon neutrality

A

when the carbon dioxide released when using the fuel is previously offset during the production of fuel.

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52
Q

reasons for carbon neutrality

A

the production of glucose via photosynthesis

6CO2(g) + 6H2O(l) -> C6H12O6(aq) + 6O2(l)

-> catalyst: UV light + chlorophyll

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53
Q

Reasons AGAINST carbon neutrality

A

other factors which contribute to carbon emmissions during the production of fuel:
- farming equipment
- transportation vehicles

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54
Q

carbohydrates

A

store/provide energy (quick energy) and fiber (remove waste)

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55
Q

Fats/oils

A

store/provide energy (slow energy), shock absorbtion/insulation, and storage of fat-soluble vitamins

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56
Q

proteins

A

helps with growth/ repair of cells, helps with immunity and transport of molecules,a nd enzymes

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57
Q

______________

A

___________________

58
Q

Redox reaction

A
  • the transfer of electrons
  • must occur in pairs
59
Q

redox half-equations

A
  • the two half equations cannot occur bu themselves. MUST OCCUR TOGETHER
  • one gives away electrons and the other takes in electrons
60
Q

OIL RIG

A

oxidation is loss
reduction is gain

61
Q

oxidation number

A
  • the hypothetical charge of an atom if the bonding is purely ionic
  • according to the OCTET rule, atoms generally want eight electrons in it’s outer shell
62
Q

oxidising agent

A

AKA (oxident)
- causes the oxidation of another substance
- UNDERGOES reduction

63
Q

reducing agent

A

AKA (reducatant)
- causes the reduction to another substance
- UNDERGOES oxidation

64
Q

congugate redox pairs (x^+/x)

A

oxident/reductant

65
Q

balancing redoox equations in ACIDIC conditions

66
Q

balancing redoox equations in BASIC conditions

A

1)KOHES
2) add OH- on both sides
3) simplify/cancel out

67
Q

net ionic equation

A

a balanced full equation with spectator ions omitted

68
Q

spectator ions

A

(ions which do not change states)
- compounds which is present but do not participate in the reaction

69
Q

where is the strongest oxident on ELECTROCHEMICAL series?

70
Q

where is the strongest reductant on ELECTROCHEMICAL series?

A

bottom RIGHT

71
Q

spontaneous slopes

A

negative slopes

IMAGINE a ball being able to roll down BY ITSELF without help
FROM THE LEFT

72
Q

what happens if there are multiple oxidents and reductants?

A

only the strongest oxidents will react with the strongest reductant

73
Q

ENERGY CONVERSATIONS:
for direct contact spontaneous redox equation

A

chemical TO thermal

74
Q

ENERGY CONVERSATIONS:
for indirect contact spontaneous redox equation

A

chemical TO electrical

75
Q

why may a reaction not occur for some metals

A
  • rate of reaction too slow

THE electrochemical series does not predict the state of reaction
the strenghts of oxident/reductant DOES NOT affect the rate of reaction

76
Q

Galvanic cell

A

an electrochemical cell that converts the chemical energy of spontaneous redox reactions into electrical energy
- reactants ARE NOT in direct contact
INDIRECT redox reaction

77
Q

3 main part/components of a galvanic cell

A
  • 2 x half cells = i galvanic cells
  • external circuit (load + wire)
  • salt bridge (internal circuts)
78
Q

electrode

A

electrical conductors, which carry electrons to/from the non-metallic part in ana eledtrolyte
- allows movement of ELECTRONS

79
Q

electrolyte

A

contains ions which can conduct electricity due to the movement of ions
- allows movement of IONS

FUNCTION: to complete the circuit by allowing the flow of charges particles through the cell

80
Q

is a gas is a product, is a gas tube required?

81
Q

Inert electrode

A

platinum (Pt) & graphite (c)

82
Q

How do you know what reaction happens at each electrode

A

AO -
anode = oxidation (-)

RC +
reduction = cathode (+)

83
Q

electron flow in galvanic

A

anode TO cathode

84
Q

internal circut

A
  • used to balance the build -up of charge

PROPERTIES:
- inert (does not react)
- soluble (does not doem a percipitate)

MOST COMMON: KNO3(aq)

85
Q

FORMULA: electromotive force (EMF)

A

E(oxident) - E(reductant) = EMF

top - bottom

CONDITIONS: slc + 1.0M

86
Q

CHANGES is size/mass of electrodes

A

at cathode mass INCREASES

at anode, mass DECREASES

87
Q

Changes in PH

(H+)

A

in OXIDATION: if concentration of H+ ions increase = more acidic = PH decrease

in REDUCTION: H+ ions increases = less basic = PH increases

88
Q

Changes in PH

(OH -)

A

in OXIDATION: concentration of ions increase = more basic = PH increase

in REDUCTION
concentraton of ions decrease = less basic = PH decrease

89
Q

Gases

A

if a gass is a product , Bubbles are formed in reaction

if gass reactant, use a gas tube

90
Q

colour

A

in OXIDATION:
- product = NI 2+
SO ion concentration increases = colour increases

in REDUCTION:
- ions are being used up = colour decreases

“more/less intesly… [colour]”
LOOK AT DATA BOOK

91
Q

Fuel cell has:

A
  • has a shared electrolyte
  • no salt bridge
  • continous suppply of reactants
92
Q

define fuel cell:

A

a galvanic cell that produces electrical energy from chemical energy, and is characterised by a continuous supply of reactants

  • uses FUEL as a reactant
93
Q

Fuel cell: overall reaction

A

combustion reaction

94
Q

Fuel cell: energy converstations

A

chemical TO electrical

95
Q

Fuel cell: electrolyte

A
  • acts similar to salt bridge, balances the build up of charge
96
Q

Fuel cell: electrolyte movement

A

cations -> cathode

anions -> anodes

97
Q

Fuel cell : oxygen + fuel

A

O: ALWAYS undergoes REDUCTION

fuel: always undergoes oxidation

98
Q

balancing half-equations for carbon containing fuels

A
  • unless specified, assume carbon containing fuel oxidises into CO2(g)
  • use KOHES to balance
99
Q

Properties of fuel cell ELECTRODES acronym

100
Q

Porous electrode

A

1) ensures that the gaseous, fuel/oxygen can come into contact with the eledtrode

2) increases surface area = increased rate of reaction

101
Q

inert electrode

A

electrode is unreactive, thus ensures that no other reaction occurs

102
Q

catalyst electrode

A

increases rate of reaction

103
Q

electrode conducts electricity

A

ensures that electrons can flow through the external circut

104
Q

energy efficiency and pollution in a fuel cell (vs power stations)

A
  1. fuel cell has direct energy conversion (chemical TO electrical)
  2. meaning less energy is wasted and thus is more efficient
  3. therefore, in comparison to a power station, less fuel is required to release tje same amount of energy . Also, therefore, less polutants and greenhouse gases would be produced
105
Q

green chemistry principle FOR fuel cells

A

1) design for energy efficiency

2) use of renewable feedstocks

106
Q

ADVANTAGES of fuel cells

A

1) more energy efficient, less fuel required

2) quiet

3) low start/stop time

107
Q

DISADVANTAGES of fuel cell

A

2) hydrogen storage/safety

108
Q

what is both inert and a catalyst in fuel cells

109
Q

is there a difference between the overall ewation in acidic & basic conditions?

A

NO, they are the exact same.

  • the charge is also the same 1.23v EMF
110
Q

PRIMARY cell

A

a galvanic cell which produces electrical energy and CANNOT be recharged

111
Q

PRIMARY cells: electrolyte purpose

A
  • to allow for the movement of ions to balance charges around the electrodes

(acts similar to the salt bridge)

  • provides the internal circuit in the cell
112
Q

what is the most common metal used in batteries

A

LITHIUM:
- it is the stronger reductant in the electrochemical series
- THUS it results in a higher EMF production

113
Q

primary vs fuel cells: type of reaction

A

both are sopntaneous

114
Q

primary vs fuel cells: reactants

A

primary: are stored in each half-cell

fuel: there is a continuous supplu of reactants

115
Q

primary vs fuel cells: electrodes

A

P: conduct electricity

F: PICCY

116
Q

primary vs fuel cells: reactivity of electrodes

A

P: may participate in the chemical reaction

F: will not participate in the chemical reaction

117
Q

primary vs fuel cells: price

A

P: cheap

F: expensive

118
Q

primary vs fuel cells: electrolyte

A

P: each half cell has its own electrolyte BUT they may also share an electrolyte

F: shared electrolyte

119
Q

primary vs fuel cells: energy efficency

A

BOTH hsve high energy efficiency because they both have direct energy conversions from chemical to electrical

120
Q

electric charge

A

the amount of charged particles (e.g electrons) that are present

  • denoted by: Q
  • si units: columbs (C)
121
Q

electric current

A

the rate of flow of charged particles per second

  • denoted by: I
  • si units: amps (A)
122
Q

electrical charge FORMULA

123
Q

Faraday’s first law of electrochemistry

A

Q is DIRECTY proportional to mass

  • eg. as MORE electrical charge passes throught he cell, the amount of substance that react/are produced also INCREASES
124
Q

elementary charge

A

the charge carried by the elementary particle (electrons)

value: -/160 x 10 ^-19

125
Q

faraday’s constant

A

the quantity of charge carried by one more of electrons

  • 96500 C / mol
126
Q

FORMULA linking electric charge and moles of electrons

A

n(e^-) = Q / F

127
Q

Farafay’s second law of electrochemistry

A

TO consider the stoichiometric ratio between n(e^-) : n(metals)

128
Q

STEPS to derive a charge of a ion

A

1) find n(metal) by n(metal) = m/Mr

2) find n(e^-) by Q/F

3) find stoichometric ration by divinding the smallest number present

129
Q

intramolecular bonding

A

within molecules

130
Q

TYPES of intramolecular bonds

A

ionic bonding

covalent bonding

metallinc bonding

131
Q

intermolecular bonding

A

between molecules

132
Q

TYPES of intermolecular bonds

A
  1. dispersion forces
  2. dipole - dipole
  3. hydrogen bonds
133
Q

what are dispersion forces?

A

Dispersion forces are weak attractions caused by temporary electron shifts in molecules.

134
Q

what are dipole-dipole forces?

A

Dipole-dipole forces are attractions between polar molecules due to their partial positive and negative charges.

They are stronger than dispersion forces but weaker than hydrogen bonds.

135
Q

what are hyrdogen bonds?

A

Hydrogen bonds are strong dipole-dipole attractions between molecules containing H bonded to N, O, or F.

They are stronger than regular dipole-dipole forces but weaker than covalent bonds.

136
Q

differences within fuel vs galvanic experiments

A

1) continuous supply vs fixed amount of reactants
2) electrodes act as catalyst and inert vs electrodes may be consumed part of reaction
3) more energy efficient vs efficiency may vary and typically decrese as cell discharges

137
Q

possible random errors

A

1) enviromental conditions: changes in temp, humidity or air pressure can affect the experiement -> leads to flunctuation in reaction rates and measuremnts

2) variations in readings of measurements: MAY be due to human error or equipment sensitivity. EG. slight changes in voltages reading

138
Q

possible systematic errors

A

1) equipment may not be properly calibrated (voltmeters/thermometers/PHmeters) or innacurate timers = lead to consistent deviations in measuremnts

2) worn or improperly prepared elctrodes = consistent errors in measurements = affecting the cell’s performance

139
Q

sample resopnse for fuel cell vs conbustion

A

direct energy conversion from chemical →
electrical energy.

LESS energy loss, MORE energy efficient.
LESS fuel is required in a fuel cell
to produce the SAME amount of
energy.
Less overall CO2 emissions overall.