Organic 2 Flashcards

1
Q

How is cracking carried out?

A

Hydrocarbons are vaporised then passed over a catalyst (silica/alumina) at a high temperature (600C- 700C)

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2
Q

Compared to alkanes, alkenes:

  • boiling point
  • saturated/unsaturated
  • flammability
  • viscosity
  • bromine water test
  • volatility
A
Have lower boiling points
Are unsaturated 
Are more flammable
Are less viscous 
Will turn from orange-> colourless in bromine water
Are more volatile
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3
Q

Paraffin oil represents

A

Alkanes

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4
Q

The product represents

A

Alkenes

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5
Q

Definition of a monomer

A

A molecule that can join with many others to make a polymer

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6
Q

Problems with disposal of addition polymers

A

Plastics are inert and non biodegradable (cannot be broken down by living organisms).
One way to get rid of plastic waste is by burning it, however this can release toxic gases.

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7
Q

What makes alkenes unsaturated?

A

They do not only have single bonds and contain a carbon (C=C) double bond.

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8
Q

Bromine test for alkenes

result + explanation

A

Orange -> colourless

Dibromoalkenes are produced because the C=C bond breaks

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9
Q

Alkane test for bromine water result + explanation

A

No colour change because alkanes are highly unreactive.

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10
Q

Why is cracking necessary?

A

It helps to match the supply of fractions with the demand for them. Shorter chained hydrocarbons have a higher demand in the industry than longer chained hydrocarbons.

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11
Q

Definition of biodegradable

A

Can be broken down by living organisms

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12
Q

Alkenes functional group

A

> C=C

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13
Q

What conditions are needed for the reaction of steam with alkenes?

A
  • 300 C
  • 60-70 atm pressure
  • catalyst of phosphoric acid
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14
Q

What kind of reaction do alkanes undergo and what conditions are needed for this to happen?

A

Substitution reactions - UV light is needed

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15
Q

What kind of reactions do alkenes undergo?

A

Addition reactions

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16
Q

Explain the addition reaction between alkenes and bromine

A
  • the bromine molecule breaks up and ‘adds’ to the alkene using the electrons from the double bond
  • the product is now saturated
  • alkanes cannot do this as they don’t have a double bond