2.5 Hydrocarbons Flashcards

1
Q

What are the only products when a
hydrocarbon fuel undergoes complete
combustion?

A

Water (H2O) and carbon dioxide (CO2)

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2
Q

Write a balanced chemical equation for the complete combustion of ethane

A

2C2H6 + 7O2 → 4CO2 + 6H2O

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3
Q

Write a balanced chemical equation for the complete combustion of ethane

A

2C2H6 + 7O2 → 4CO2 + 6H2O

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4
Q

When does incomplete combustion occur? What is required to ensure complete combustion occurs?

A

Incomplete combustion occurs when there is an insufficient supply of oxygen.
To ensure complete combustion occurs, the
reaction should be carried out with excess oxygen.

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5
Q

What are the products of incomplete
combustion?

A

Carbon particulates - soot (C)
Carbon dioxide (CO2)
Carbon monoxide (CO)
Water (H2O)

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6
Q

Write a balanced symbol equation for the
incomplete combustion of methane to
form carbon monoxide and water

A

2CH4 + 3O2→ 2CO + 4H2O

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7
Q

Write a balanced symbol equation for the
incomplete combustion of methane to
form carbon monoxide and water

A

2CH4 + 3O2→ 2CO + 4H2O

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8
Q

advantages of fossil fuels

A

produces large amounts of energy
currently relatively easily available

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9
Q

disadvantages of fossil fuels

A

uses infinite resources
releases CO2 which contributes to global warming
releases carbon monoxide which is toxic
produces acidic gases which causes acid rain

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10
Q

incomplete combustion eg propane

A

propane + oxygen—>carbon dioxide + carbon monoxide

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11
Q

What type of bonds are the C-C and C-H
bonds in alkanes?

A

σ-bond
(Sigma bond)

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12
Q

Give an example of a type of reaction
that uses a radical substitution
mechanism?

A

photochlorination of alkanes

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13
Q

What is a photochlorination reaction?

A

A photochlorination reaction occurs when
one of the hydrogen atoms on an alkane
is replaced by a chlorine atom. The
reaction is initiated by light.

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14
Q

Compare the difference in reactivity of
alkanes and alkenes

A

Alkenes have a high electron density in the
carbon-carbon double bond, C=C. This makes
them more susceptible to attacks from
electrophiles, compared to alkanes, making
alkenes more reactive.

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15
Q

Describe the C=C bond in alkenes in
terms of the types of covalent bonds
present

A

The C=C has a normal σ-bond as well as a π-bond located above and below the σ-bond.
σ-bond: sigma bond
π-bond: pi bond

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16
Q

What is stereoisomerism (in terms of E-Z
isomerism)?

A

Stereoisomerism occurs when isomers have the same structural formula but a different arrangements of atoms in space due to the limited rotation around the carbon-carbon double bond.
Isomers are normally referred to as E- or Z- isomers.

17
Q

How do you determine whether an isomer is E- or Z-?

A

● In E- isomers, high priority groups are on
opposite sides of the C=C bond.
● In Z- isomers, high priority groups are on the same side of the C=C bond.

18
Q

Why can alkenes undergo electrophilic
addition?

A

Alkenes are susceptible to attack from
electrophiles because of the high
electron density in the C=C double bond

19
Q

Which qualitative tests can be carried out
to test for alkenes?

A
  • Add bromine water: The orange solution decolourises if the alkene C=C bond is present.
  • Add acidified potassium dichromate: The purple solution decolorises if the alkene C=C bond is present.
20
Q

Explain why the electrophilic addition of
bromine to propene can produce a major
and a minor product

A

When propene undergoes electrophilic addition, two possible products can be formed: the major and the minor product. This is because two different carbocation intermediates can be formed - the primary and the secondary carbocation. The secondary carbocation is more stable so this produces the major product
2- bromopropene. The primary carbocation forms the minor product 1-bromopropane.

21
Q

What reaction does an alkene undergo to form an alkane? Name the reagents and conditions

A

● Reaction type: Hydrogenation
● Reagents: Hydrogen gas, H2
● Conditions: Nickel catalyst, 150℃

22
Q

What is addition polymerisation?

A

Addition polymerization occurs when lots of monomers with carbon-carbon double bonds join together to form a long-chain polymer.
The 𝝅 bond breaks and the electrons are used to form 𝛔 bonds with other monomers on either side of it.
Atom economy is 100%.

23
Q

what is a repeat unit?

A

A single unit of a polymer derived from its monomer, the repetition of which
would result in the polymer.