Alkenes Flashcards

1
Q

What do alkenes contain?

A

One or more carbon-to-carbon double bond

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2
Q

What is the general formula of aliphatic hydrocarbons?

A

C(n)H(2n)

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3
Q

Where is a pi bond formed from?

A

The sideways overlap of two p-orbitals one from each carbon atom of the double bond

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4
Q

Where is pi bond electron density concentrated?

A

Above and below the plane of nuclei of bonded atoms

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5
Q

What do pi bonds prevent? How?

A

Rotation around the double bond, due to the lock of the two carbon atoms leading to concentrated electron density above and below the plane of atom.

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6
Q

What is the shape around the carbon atoms in double bond of an alkene?

A

Trigonal Planar- three areas of electron density around each of the carbon atoms

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7
Q

Define stereoisomers

A

Same structural formula but a different arrangement of the atoms in space

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8
Q

Why does stereoisomerism occur?

A

Due to the restricted rotation around the double bond, and therefore the groups attached to each carbon are fixed relative to each other.

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9
Q

What two conditions have to be fulfilled for E/Z isomerism?

A

A C=C double bond

Different groups attached to each carbon atom of the double bond

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10
Q

What condition has to be different for cis-trans isomerism than E/Z isomerism?

A

In cis-trans isomerism one of the attached groups on the each carbon atom on the double bond must be the same.

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11
Q

What does a cis-isomer have?

A

The hydrogen atoms and methyl groups on each carbon in the double bond are on the same side.

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12
Q

What doe a trans-isomer have?

A

The hydrogen atoms and methyl groups on each carbon in the double bond are opposite each other.

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13
Q

What occurs in a Z isomer?

A

The groups with higher priority are on the same side

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14
Q

What occurs in a E isomer?

A

The groups with higher priority are diagonally placed across the double bond

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15
Q

How is priority assigned?

A

Based on atomic number. The higher the atomic number, the higher the priority.

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16
Q

What happens if the atom attached to carbon atom is the same when assigning priority?

A

Keep going along the molecule until reaches a difference

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17
Q

Why are alkenes more reactive than alkanes?

A

Pi bonds are the overlap of p orbitals above and below the plane of the sigma bond. Being above and below means more exposed electrons. Reacts more easily.

18
Q

What conditions are needed in the hydrogenation of an alkene?

A

423K

Nickel Catalyst

19
Q

What is hydrogenation?

A

The addition of H2 across a double bond

20
Q

How is unsaturation tested for?

A

Addition of bromine water. Colour change from orange to colourless if a double bond is present.

21
Q

What conditions are required for hydration of alkenes?

A

Steam

Concentration phosphoric acid catalyst

22
Q

Define ‘electrophilic addition’

A

An addition reaction in which the first step is attack by an electrophile on a region of high electron density

23
Q

Where is high electron density found?

A

Double bond of the alkene

24
Q

Define ‘electrophile’

A

An atom or group of atoms that is attracted to an electron rich centre and accepts an electron pair

25
What is a carbocation?
Containing a positively charged carbon atom
26
What is the most stable carbocation?
Tertiary carbocation
27
What makes a carbocation more stable?
Each alkyl group pushes electrons towards the positive charge of carbocation Positive charge is spread over alkyl groups More alkyl group= more spread of charge= more stable
28
What does Markownikoff's rule state?
When a compound HX is added to an unsymmetrical alkene, the hydrogen becomes attached to the carbon with the most hydrogens attached to it already.
29
What are polymers?
Long chains of repeating units of monomers
30
What type of polymerisation do alkenes undergo?
Addition polymerisation to produce long saturated chains containing no double bonds.
31
How does recycling alkene based polymers help?
Reduces environmental impact Conserves finite fossil fuels Reduces waste in landfill
32
How are polymers recycled?
``` Discarded polymers are sorted by type Polymers chopped into flakes Washed Dried Melted Recycled polymers cut into pellets ```
33
Why is disposal of PVC hazardous?
High chlorine content
34
What does PVC produce when burnt?
Corrosive hydrogen chloride gas
35
How is PVC disposed of?
Solvents dissolve polymer | High grade polymers are recovered by precipitation from the solvent
36
What is feedstock recycling?
Chemical and thermal process of reclaiming monomers from waste polymers
37
What is the biggest advantage of feedstock recycling?
Can handle unsorted and unwashed polymers
38
What are bioplastics?
Plastics produced from plant starch, cellulose, plant oils and proteins which are renewable and sustainable.
39
How are biodegradable polymers broken down?
By microorganisms into carbon dioxide, water and biological molecules
40
What are photodegradable polymers?
Polymers containing bonds that are weakened by absorbing light to start degradation