Unit 3: Section 3 - Alkenes and Alcohols Flashcards

1
Q

Why type of hydrocarbon is an alkene?

A

An unsaturated hydrocarbon.

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2
Q

What does unsaturated mean?

A

It means they are able to form more bond under the correct conditions.

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3
Q

Why do carbon-carbon double bonds have a high electron density?

A

Because there are two pairs of electrons present.

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4
Q

What are electrophiles?

A

Electron-pair acceptors

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5
Q

What are polymers formed from?

A

Monomers

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6
Q

How are addition polymers made?

A

When monomers join together to make long chains.

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7
Q

What are polyalkenes?

A

Addition polymers made from alkenes.

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8
Q

Why are addition polymers unreactive?

A

They are saturated and the main carbon chain is non-polar.

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9
Q

What forces hold polyalkene chains together?

A

Van der Waals forces

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10
Q

____, ________ polyalkene chains tend to be ______ and ______.
_____, _________ polyalkene chains tend to be _______ and ______________.

A
Long
Straight
Strong
Rigid
Short
Branched
Weaker
More flexible
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11
Q

What does a plasticiser do and how does it work?

A

They make polymers more flexible by pushing polymer chains apart and reducing the strength of the intermolecular forced between the chains.

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12
Q

What is PVC used to make? (2)

A
  • Drainpipes

* Window frames

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13
Q

What is plasticised PVC used to make?

A
  • Electrical cable insulation
  • Flooring tiles
  • Clothing
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14
Q

How do you determine whether an alcohol is primary, secondary or tertiary?

A

By looking at which carbon the hydroxyl group is bonded to.

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15
Q

What is a biofuel?

A

A fuel that’s made from biological material that’s recently died.

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16
Q

What are the advantages of using biofuels? (2)

A
  1. Biofuels are renewable energy sources. Unlike fossil fuels, biofuels won’t run out, so they’re more sustainable.
  2. Biofuels are classed as carbon neutral so they produce carbon dioxide which is then absorbed by plants.
17
Q

What does carbon neutral mean?

A

Carbon neutral means that they do not contribute to or remove the carbon dioxide in the atmosphere.

18
Q

What are the disadvantages of using biofuels? (2)

A
  1. Petrol car engines have to be modified to use fuels with a high ethanol concentration.
  2. When land is used to grow crops for fuel that land isn’t being used to grow food.
19
Q

How do you oxidise alcohol? (2)

A
  1. By burning them.

2. By using an oxidising agent such as acidified potassium dichromate (VI)

20
Q

What do determines what an alcohol oxidises to?

A

The structure of the alcohol

21
Q

Which type of alcohol oxidises to what?

A
  • Primary alcohols oxidise to aldehydes and then carboxylic acids.
  • Secondary alcohols oxidise to ketones.
  • Tertiary alcohols do not oxidise.
22
Q

Why do tertiary alcohols not oxidise easily?

A

They don’t react with potassium dichromate. You can only oxidise them by burning them.

23
Q

How do you oxidise a secondary alcohol?

A

Using potassium dichromate under reflux.

24
Q

How can you distinguish between aldehydes and ketones?

A
  • Fehling’s solution

* Tollens’ reagent

25
Q

How do you produce a carboxylic acid?

A

Oxidise a primary alcohol under reflux using potassium dichromate.

26
Q

How do you produce an aldehyde?

A

Distill a primary alcohol after it has been oxidised by potassium dichromate.

27
Q

How does Fehling’s solution distinguish aldehydes and ketones?

A

Fehling’s solution is a deep blue solution which stays blue with a ketone and changes to brick red when an aldehyde is present.

28
Q

How does Tollens’ reagent distinguish aldehydes and ketones?

A

Tollens’ reagent turns silver in the presence of an aldehyde but not in the presence of a ketone.