2.5 Hydrocarbons Flashcards

1
Q

What is the equation for combustion of ethane?

A

C2H6 + 3 1/2 O2 —> 2CO2 + 3H2O

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2
Q

What is the equation for the incomplete combustion of ethane?

A

C2H6 + 2 1/2 02 —-> 2CO + 3H20

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3
Q

What is halogenation?

A

a reaction between an organic compound and any halogen (member of group 7)

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4
Q

What are the three steps of halogenation?

A
  1. Initiation
  2. Propagation
  3. Termination
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5
Q

What is a radical?

A

a highly reactive species with an unpaired electron.

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6
Q

What occurs in the initiation stage of halogenation between an example of methane and chlorine?

A

Ultraviolet light has sufficient energy to break the Cl–Cl bond within Cl2 (homolytic fission thus both Cls receives one of the bond electrons), as a result radicals are formed.

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7
Q

What occurs in the propagation stage of halogenation of an example of methane and chlorine?

A

A propagation reaction uses a radical as a reactant and then forms a radical as a product. This means that the reaction continues. It is therefor called a chain reaction.

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8
Q

What occurs in the termination stage of halogenation of an example of methane and chlorine?

A

The propagation step continues until two radicals meet, then the reaction stops (termination stage)
This stage the two radicals create a compound with no radical.

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9
Q

Use a whiteboard and write out the free radical substitution mechanism.

A

of chlorine

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10
Q

Discuss the structures of alkenes:

A

They are unsaturated so contain a double bond and are thus much more reactive than alkanes.

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11
Q

Discuss ethene:

A

4 electrons available for bonding, three are normal covalent sigma bonds using both the carbons s orbital electrons and 1 p orbital. This means there are three bond pairs of electrons around each carbon resulting in a trigonal planar shape with bond angles of 120 degrees. The overlapping p bond creates pie bonds above and below the plane of the molecule which restrics the movement creating E-Z isomers.

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12
Q

When does E-Z isomerism occur?

A

In alkenes where each end of the C=C has two different groups bonded to it.

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13
Q

Why are alkenes susceptible to electrophilic attack?

A

as they have a pair of electrons in a pie orbital that makes them susceptible to attack from an electrophile (+)

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14
Q

What is an electrophile?

A

An electron deficient species that can accept a lone pair of electrons.

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15
Q

What is heterolytic bond fission?

A

When a bond breaks and one of the bonded atoms receive both electrons thus ions are formed.

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16
Q

Write the mechanism of electrophilic addition of HBr to ethene.

18
Q

which is the major product of the electrophilic addition of propene, 2-bromopropane or 1-bromopropane and why?

A

2-bromopropane as the cation releases a delta plus that can spread around so position 2 has better potential spread than position 1 thus making it more STABLE. (the cations stability goes: primary<secondary<tertiary)

19
Q

What is the test for alkenes?

A

Bromine water is used and if alkenes are present it goes from brown to colourless.

20
Q

What is hydrogenation?

A

Alkene + hydrogen with a nickel catalyst to make saturates oils to make butter substitues.

21
Q

Name three useful polymers:

A
  • polypropene for food containers
  • polychloroethene for water pipes
  • polyphenylethene or polystyrene is used for packaging.