Hydrocarbons 2 Flashcards

1
Q

Halogens react with Alkanes to make Haloalkanes methane + bromine —->

A

uv light methane + bromine —-> bromomethane + hydrogen bromide

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2
Q

Halogens react with Alkenes to make Haloalkanes ethene + bromine —->

A

ethene + bromine —-> di bromoethane

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3
Q

Alcohols have the functional group OH Name 2 ways to make ethanol.

A

phosphoric acid 1. Ethene + steam —> ethanol 2. Fermentation Yeast Glucose. —> Ethanol + CO2

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4
Q

Advantages and disadvantages of using fermentation method to produce ethanol

A

Advantages glucose is a renewable source (from sugar cane) Yeast is easy to grow Disadvantages ethanol made is not very concentrated and needs distilling to increase strength (like in whisky distillaries)

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5
Q

What conditions do we need for fermentation to produce ethanol?

A

about 30 deg temp (yeast contains an enzyme) Anaerobic (oxygen converts ethanol into ethnic acid (vinegar, yuck!)

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6
Q

Advantages and disadvantages of using the ethene and steam method to produce ethanol

A

ethene comes from crude oil which is non-renewable

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7
Q

What conditions do we need for ethene and steam to produce ethanol?

A

a catalyst of phosphoric acid high temp 300 deg high pressure 65 atmospheres

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8
Q

What is the functional group of carboxylic acids?

A

COOH

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9
Q

Carboxylic acids react like all acids to make salt + water. What is the name of the salt made by reacting ethanoic acid and sodium carbonate?

A

ethanoic acid + sodium carbonate–>sodium ethanoate + water + CO2

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10
Q

What is the functional group of an ester?

A

COO

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11
Q

How do we make an ester?

A

ethanoic acid + ethanol —> ethyl ethanoate + water

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12
Q

What is an addition polymer?

A

Made by joining unsaturated molecules of alkenes

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13
Q

How do you draw the repeat unit of a polymer?

A

remove double bond and replace with single put brackets round whole molecule add the single bonds on left and right write n at bottom right of bracket

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14
Q

Why are most polymers hard to get rid of?

A

They are inert and don’t react easily because carbon-carbon bonds are very strong takes a long time to biodegrade During them releases toxic gases Best to reuse them not dispose of them

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15
Q

Give an example of a condensation polymer?

A

polyester

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16
Q

What do we call a biodegradable polyesters?

A

biopolyesters

17
Q

What are the two types of polymers?

A

Addition and condensation

18
Q

What are addition polymers made from?

A

Alkenes

19
Q
  • Describe how you can draw the repeat unit of a polymer
A
  • First one is going from double bond to single bond
  • Brackets outside and ‘n’ bottom right
  • Second one is going from a polymer to monomer
  • But in the double bond and write the ‘n’ on the left
20
Q

What are condensation polymers made from?

A
  • Acids and other shit which is a waste of time to learn (I have better things to do with my life)