2.5 Hydrocarbons Flashcards

1
Q

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

A

Water (H(2)O) and carbon dioxide (CO(2)).

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2
Q

Write a balanced chemical equation for the complete combustion of ethane

A

2C(2)H(6) + 7O(2) → 4CO(2) + 6H(2)O

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3
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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4
Q

What are the products of incomplete combustion?

A

Carbon particulates - soot (C)
Carbon dioxide (CO(2))
Carbon monoxide (CO)
Water (H(2)O)

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5
Q

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

A
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6
Q

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

A
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7
Q

What are the benefits and drawbacks related to the burning of fossil fuels for energy?

A
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8
Q

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

A

σ-bond
(Sigma bond)

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9
Q

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

A

Photochlorination of alkanes

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10
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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11
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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12
Q

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

A
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13
Q

What is Streoisomerism (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.

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14
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.

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15
Q
A
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16
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

17
Q

Describe the electrophilic addition of bromine to ethene, including diagrams.

A
18
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 decolourises if the alkene C=C bond is present.

19
Q

Give the mechanism for the electrophilic addition of hydrogen bromide to propene

A
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-bromopropane. 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
22
Q

What is addition polymerisation?

A

Addition polymerisation 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 either side of it.
Atom economy is 100%.

23
Q

What is a repeat unit?

A