Alkanes Flashcards

1
Q

alkane properties

what are the general properties of alkanes

A
  • saturated hydrocarbons
  • CnH2n+2
  • produced from crude oil
  • used for fuels
  • covalent bonds between the atoms however weak VDWs between molecules
  • around each C atom there is a tetrahedral shape with bond angle 109.5
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2
Q

alkane properties

what happens when you boil a liquid alkane

A

energy is needed to break the induced dipole-dipole attraction (VDWs) forces between the molecules in order to seperate them

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3
Q

alkane properties

what happens to the boiling point of alkanes as carbon chain length increases

A
  • as the C chain length increases the boiling point increases
  • because there is more surface contact between the molecules
  • so there are more Van der Waal forces between molecules
  • which need more energy to overcome
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4
Q

alkane properties

what happens to the boiling point of alkanes as branching occurs

A
  • a branches isomer has a lower boiling point than the unbranched isomer
  • in a more branched alkane, there is less surface contact between molecules leading to fewer VDW forces
  • which need less energy to break the weaker VDW forces between molecules
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5
Q

alkane properties

what is the solubility of alkanes in water

A

alkanes are immiscible (insoluble) in water - because they are non-polar, they only contain VDW and so cannot form hydrogen bonds with water

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6
Q

fractional distillation

how is crude oil seperated

A
  • by fractional distillation
  • crude oil mixture is vapourised and passed into a fractioning column with a temperature gradient ( up = cooler)
  • the gradient allows the mixture to seperate into fractions
  • as the vapours condense at levels which match their boiling points
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7
Q

cracking

what is cracking

A

process that splits long chain alkanes into shorter more valuable alkanes, alkenes and hydrogen

  • increasing branching in chains
  • increases amount of gasoline
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8
Q

cracking

what is thermal cracking

more alkenes produced this method

A
  • long-chain alkane used
  • 400-900°
  • high pressure needed
  • mainly alkenes produced and sometimes hydrogen
  • alkenes used for making polymers
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9
Q

cracking

what is catalytic cracking

A
  • long-chain alkane used
  • 450°
  • slight pressure
  • silica and aluminium oxide or zeolite catalyst
  • produces branched and cyclic alkanes and aromatic compounds
  • products used for motor fuels (short chains burn more volatilely)
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10
Q

alkenes

what is the test for alkenes

A

reagent: bromine water (brown liquid)
observation: orange to colourless

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11
Q

combustion

what is complete combustion

A

complete combustion releases CO2 and H2O because the fuel is fully oxidised

this occurs when there is an excess of oxygen

alkane + oxygen = carbon dioxide + water

C3H8 + 5O2 = 3CO2 + 4H2O

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12
Q

combustion

what is incomplete combustion

A

incomplete combustion can produce either carbon monoxide or carbon

this occurs when there is a limited supply of oxygen and produces less energy per mole than complete combustion

alkane + oxygen = carbon monoxide + water
alkane + oxygen = carbon + water

C3H8 + 3.5O2 = 3CO +4H2O
C3H8 + 2O2 = 3C + 4H2O

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13
Q

combustion

what is the effect and solution of the production of carbon dioxide

produced by complete combustion of fuels

A

effect - greenhouse gas that contributes to global warming

solution - burn less fuel or use carbon offsetting

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14
Q

combustion

what is the effect and solution of the production of carbon monoxide

produced by incomplete combustion of fuels

A

effect - a toxic gas that bonds to haemoglobin, reducing the capacity of oxygen

solution - ensure a plentiful supply of oxygen or use a catalytic converter

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15
Q

combustion

what is the effect and solution of the production of carbon particulates

produced by incomplete combustion of fuels

A

effect - black solid causes respiratory irritation, lung disease and global dimming

solution - ensure a plentiful supply of oxygen or use a catalyctic converter

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16
Q

combustion

what is the effect and solution of the production of sulphur dioxide

produced by burning fuels that contain sulfur (mainly coal)

A

effect - it is an acidic gas that can dissolve in water to produce acid rain
SO2 + 1/2 O2 = H2O + H2SO4

solution - flue-gas desulfurization

17
Q

combustion

what is the effect and solution of the production of oxides of nitrogen

NOx are produced by nitrogen and oxygen reacting

occurs at high temperatures e.g inside a car engine

A

N2 + O2 = 2NO

effect - NOx are acidic gases that can cause acid rain, photochemical smog and respiratory irritation

solution - catalytic converters

18
Q

free radical substitution

what is free radical subtitution

A

*reagents: *halogen (Cl2 or Br2 or I2) and excess alkane
*conditions: *UV radiation or 300°

  • it is a substitiution reaction as H atom in the alkane molecule is replaced
  • the Cl-Cl and C-H bonds break by homolytic fission to form radicals
  • a radical is a specied with an unpaired electron
19
Q

free radical substitution

what are the 3 steps involved in FRS

A
  1. initiation
  2. propagation
  3. termination
20
Q

free radical substitution

what happens during initiation

A

breaking of the Cl-Cl bond by homolytic fission to make 2 chlorine radicals

the UV radiation provides the energy needed to break the Cl-Cl bond

21
Q

free radical substitution

what happens during propagation

A

a very reactive chlorine radical attacks a methane molecule in a chain reaction

chlorine radical is used up in the first step, but is regenerated in the second
it is now able to attack a new methane molecule

22
Q

free radical substitution

what happens during termination

A

reaction ends when any two radicals combine forming a new molecule

23
Q

free radical substitution

what are the limitations of FRS

A
  • leads to the formation of a mixture of products
  • further substitution produces a mixture of halogenoalkanes
  • reactions can occur at different positions in the carbon chain
24
Q

free radical substitution

what are the disadvantages of FRS

A
  • low % yield of desired halogenoalkane
  • seperation by fractional distillation which is costly

the minimise further substitution an excess of methane is used