Alkanes (Edexcel A Level Chemistry): Flashcards

Exam code: 9CHO

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  • Define hydrocarbon.

Cards in this collection (45)

  • Define hydrocarbon.

    A hydrocarbon is a compound containing hydrogen and carbon atoms only.

  • True or False?

    Arenes are classified as aliphatic hydrocarbons.

    False.

    Arenes are classified as aromatic hydrocarbons, not aliphatic. Alkanes, alkenes, and alkynes are aliphatic.

  • What does the "alk" portion of an alkane name indicate?

    The "alk" portion indicates the number of carbon atoms in the chain (e.g. meth = 1, eth = 2, prop = 3, but = 4, pent = 5).

  • What is the general molecular formula of alkanes?

    Alkanes have the general molecular formula CnH2n+2.

  • True or False?

    Alkanes are described as aliphatic hydrocarbons.

    True.

    Alkanes (along with alkenes and alkynes) are described as aliphatic, meaning they are non-aromatic hydrocarbons. Arenes are aromatic.

  • Alkanes contain only .......... bonds, are described as .......... hydrocarbons, and have no .......... group.

    Alkanes contain only single bonds, are described as aliphatic hydrocarbons, and have no functional group.

  • What does it mean for an alkane to be saturated?

    A saturated compound contains only single carbon-carbon bonds, with no double or triple bonds.

  • What three structural arrangements can alkanes adopt?

    Alkanes can be linear, branched, or cyclic in structure.

  • Define fractional distillation in the context of crude oil refining.

    Fractional distillation is a separation technique in which the hydrocarbons in crude oil are separated into fractions based on their boiling points.

  • Why are straight-chain alkanes reformed before use as fuel?

    Straight-chain alkanes are more likely to explode rather than combust smoothly in an engine, causing knocking, which makes combustion less efficient.

  • True or False?

    Crude oil is a pure compound of alkanes.

    False.

    Crude oil is a mixture of hydrocarbons including alkanes, cycloalkanes, and arenes. It must be separated by fractional distillation before use.

  • What is cracking in the context of oil refining?

    Cracking is the process of breaking down large, heavy hydrocarbon fractions into smaller, more useful alkanes and alkenes with lower relative formula mass.

  • Thermal cracking requires temperatures up to .......... °C and pressures up to .......... atmospheres, and produces a lot of ...........

    Thermal cracking requires temperatures up to 1000 °C and pressures up to 70 atmospheres, and produces a lot of alkenes.

  • What is reforming of alkanes?

    Reforming is the conversion of straight-chain alkanes into branched alkanes or cycloalkanes to reduce knocking in engines. It typically uses a platinum catalyst.

  • What conditions are used in catalytic cracking?

    Catalytic cracking uses a temperature of around 450°C, slight pressure, and a catalyst such as a zeolite or aluminium oxide. It mainly produces aromatic hydrocarbons.

  • True or False?

    Thermal cracking produces mainly aromatic hydrocarbons.

    False.

    Thermal cracking produces alkanes and a large proportion of alkenes. It is catalytic cracking that mainly produces aromatic hydrocarbons.

  • Why is cracking of heavier oil fractions commercially important?

    Smaller hydrocarbon fractions such as gasoline are in higher demand than heavier fractions. Cracking converts excess heavy fractions into more useful, lower-Mr alkanes and alkenes.

  • Define complete combustion of an alkane.

    Complete combustion occurs when an alkane burns in excess oxygen, producing only carbon dioxide and water.

  • How does photochemical smog form from car exhaust emissions?

    Nitrogen oxides (NOx) react with volatile organic compounds (VOCs) in the atmosphere to form peroxyacetyl nitrate (PAN), the main pollutant in photochemical smog.

  • True or False?

    Carbon monoxide is toxic because it binds strongly to haemoglobin.

    True.

    Carbon monoxide binds strongly to haemoglobin, preventing it from transporting oxygen to organs and removing carbon dioxide as waste. This can cause death.

  • In a car engine, .......... and .......... react at high temperatures and pressures to form oxides of nitrogen, released in .......... fumes.

    In a car engine, nitrogen and oxygen react at high temperatures and pressures to form oxides of nitrogen, released in exhaust fumes.

  • How do nitrogen oxides from car exhausts contribute to acid rain?

    Nitrogen oxides dissolve and react with water and oxygen in the atmosphere to form nitric acid, which falls as acid rain, corroding buildings and harming aquatic life.

  • Define incomplete combustion of an alkane.

    Incomplete combustion occurs when an alkane burns in a limited supply of oxygen, producing carbon monoxide and/or carbon (soot) alongside water.

  • True or False?

    Incomplete combustion occurs in car engines because oxygen supply is limited.

    True.

    Inside a car engine the oxygen supply is restricted, so incomplete combustion takes place, producing toxic carbon monoxide and carbon soot alongside water.

  • What are three harmful effects of carbon particulates from incomplete combustion?

    Carbon particulates can cause respiratory damage when inhaled, coat buildings (accelerating corrosion), and cause global dimming by reflecting sunlight back into space.

  • What is photochemical smog?

    Photochemical smog is atmospheric pollution formed when nitrogen oxides react with volatile organic compounds (VOCs) in sunlight to produce peroxyacetyl nitrate (PAN).

  • What is a catalytic converter?

    A catalytic converter is a device fitted to car exhausts that uses precious metals (such as platinum) on a honeycomb surface to convert toxic exhaust gases into less harmful products.

  • Give two benefits of using biofuels over fossil fuels.

    Biofuels are renewable and roughly carbon neutral. They can also reduce waste going to landfill (for biodiesel and biogas) and provide economic opportunities for less developed countries.

  • In a catalytic converter, carbon monoxide and nitrogen monoxide react to form carbon dioxide and .......... gas, which is .......... and .......... to the atmosphere.

    In a catalytic converter, carbon monoxide and nitrogen monoxide react to form carbon dioxide and nitrogen gas, which is unreactive and harmless to the atmosphere.

  • True or False?

    Biofuels are completely carbon neutral.

    False.

    Biofuels are often considered carbon neutral because plants absorb CO2 as they grow. However, CO2 is also produced during refining and transport, so they are not fully carbon neutral.

  • Why do catalytic converters use a honeycomb structure?

    The honeycomb structure provides a very large surface area for the precious metal catalyst (e.g. platinum), maximising contact with exhaust gases and improving the efficiency of reactions.

  • Define biofuel.

    A biofuel is a renewable fuel derived from living matter. The three main types are biodiesel, bioethanol, and biogas.

  • Give two drawbacks of using biofuels.

    The cost of converting engines to run on biofuels is high. In developed countries, land needed to grow biofuel crops conflicts with food production.

  • True or False?

    The platinum in a catalytic converter acts as a homogeneous catalyst.

    False.

    The platinum in a catalytic converter is a heterogeneous catalyst: it is in a different phase (solid) from the gaseous exhaust reactants. It is coated on a honeycomb to maximise surface area.

  • How is bioethanol produced?

    Bioethanol is produced by fermentation of plant sugars. It is a renewable biofuel that can be used as a substitute for or additive to petrol.

  • Define a free radical.

    A free radical is a highly reactive species with an unpaired electron, formed by homolytic fission of a covalent bond.

  • Why does free radical substitution not produce a pure halogenoalkane?

    Free radical substitution produces a mixture of products because further substitution can occur if excess halogen is present, and because substitution can occur at different carbon atoms in the chain.

  • What is homolytic fission?

    Homolytic fission is the breaking of a covalent bond in which each atom receives one electron from the shared pair, producing two free radicals.

  • What are the three steps of free radical substitution in order?

    The three steps are initiation (homolytic fission by UV light), propagation (chain reaction forming halogenoalkane), and termination (two radicals combine to stop the reaction).

  • True or False?

    The propagation step consumes free radicals without regenerating them.

    False.

    The propagation step regenerates free radicals in each cycle, allowing the chain reaction to continue. Free radicals are only consumed permanently in the termination step.

  • In propagation, a halogen radical attacks an alkane, breaking a C-H bond by .......... fission to form an .......... radical, which attacks a halogen molecule to regenerate a .......... radical.

    In propagation, a halogen radical attacks an alkane, breaking a C-H bond by homolytic fission to form an alkyl radical, which attacks a halogen molecule to regenerate a halogen radical.

  • What occurs during the initiation step of free radical substitution?

    The initiation step is where UV light provides energy to break the Cl-Cl or Br-Br bond by homolytic fission, producing two halogen free radicals.

  • True or False?

    Free radical substitution of alkanes can occur in the dark without UV light.

    False.

    Alkanes are very unreactive, so UV light (sunlight) is required to provide the energy needed to initiate free radical substitution by breaking the halogen-halogen bond.

  • What occurs in the termination step of free radical substitution?

    The termination step is where two free radicals combine to form a single unreactive molecule, ending the chain reaction.

  • Give an example of an impurity formed in the termination step when chlorinating methane.

    If two methyl radicals (CH3•) combine, ethane (CH3CH3) is formed as an impurity instead of the target chloroalkane.

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