Alkenes Flashcards

1
Q

General formula

A

CnH2n

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2
Q

Saturated or unsaturated?

A

Unsaturated - contain a C=C bond

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3
Q

What does the double bond consist of?

A

Sigma σ and Pi covalent bonds.

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4
Q

Which of the two bonds is stronger?

A

σ - sigma bonds are stronger than Pi bonds. The C=C is stronger than the C-C.

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5
Q

Which is longer?

A

C=C bond length is shorter than the C-C

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6
Q

How are σ bonds formed? And draw them

A

From the LINEAR overlap of 2 s-orbitals, an s-orbital and a p-orbital and two p-orbitals. All of which result in free rotation along the bond axis.

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7
Q

How are Pi bonds formed? and draw them.

A

The SIDEWAYS overlap of two p-orbitals, this results in restricted rotation along the bond axis.

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8
Q

What is the C=C bond a region of?

A

High electron density, which makes it open to attack from electrophiles.

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9
Q

What is more reactive alkanes or alkenes

A

Alkenes

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10
Q

What happens when alkenes undergo addition reactions?

A

The Pi bond is broken, the addition occurs across the double bond.

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11
Q

What are the conditions necessary for the complete combustion of an alkene?

A

A source of ignition and a plentiful supply of oxygen

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12
Q

Write an equation for the combustion of ethene

A

in book

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13
Q

What are the conditions for incomplete combustion?

A

A source of ignition and a limited supply of oxygen

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14
Q

Write an equation

A

in book

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15
Q

What is the name of the mechanism and draw the mechanism of the bromination of ethene.

A

Electrophilic addition - in book

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16
Q

Whats the splitting of HBr representative of?

A

Heterolytic fission

17
Q

What do alkyl groups do to a carbocation?

A

They stabilise it, therefore a tertiary carbocation is more stable than a secondary carbocation which is more stable than a primary carbocation.

18
Q

Does this affect the products made in any way

A

Yes, products that have a tertiary carbocation will be made much more than products which had a secondary etc.

19
Q

What are the conditions and products for the hydrogenation of an alkene.

A

Conditions - finely divided nickel catalyst, 180ºC and 4atm

Product - an Alkane

20
Q

What are the conditions and products for the hydration of an alkene with steam?

A

Concentrated phosphoric acid, 300ºC, 60-70atm

Ethanol

21
Q

What are the conditions and products for the bromination of an alkene with bromine water?

A

Mix bromine water with liquid alkene or bubble the alkene through bromine water
A dibromoalkane

22
Q

How do you test for a C=C bond?

A

If yellow bromine water changes to colourless the compound contains a C=C bond.

23
Q

Draw the addition polymerisation 3 vinyl chloride molecules to form one polyvinyl chloride molecule via addition polymerisation

A

in book

24
Q

What happens when you use excess reactant?

A

All the functional groups react