Topic 11 - Alcohols, Carboxylic Acids, Polymers *hard* Flashcards

1
Q

What is a homologous series?

A

A group of hydrocarbons that have the same general formula with similar chemical properties.

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2
Q

What is a functional group?

A

A group of atoms responsible for the characteristic reactions of a compound

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3
Q

what functional group do alcohols have?

A

Alcohols are a group of compounds with the functional group -OH

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4
Q

general formula of Alcohols

A

Cn H2n+1 OH

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5
Q

dehydration reaction of alcohols

A

alcohol -> alkene + water

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6
Q

what conditions are needed for dehydration reactions

A

heat and acid catalyst

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7
Q

Order of first four alcohols

A

Methanol , Ethanol, Propanol , Butanol

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8
Q

Fermentation

A

glucose -> ethanol + carbon dioxide
C6H12O6 -> 2C2H5OH + 2CO2

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9
Q

Why is yeast mixed to the solution of glucose

A

Yeast cells contain an enzyme called zymase which catalyses the reaction - speeds it up which makes it suitable for industrial processes

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10
Q

Why is the solution kept between 30 and 40 degrees

A
  • Because the rate of fermentation is fastest in these temperatures
  • At lower temperatures the reaction is too slow and if the temp is too high the yeast enzymes will denature and won’t catalyse the reaction at all
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11
Q

Why do we need to keep the mixture in anaerobic conditions

A

If the mixture is exposed to oxygen, the ethanol would oxidise to ethanoic acid which is what you get in vinegar

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12
Q

How can you keep the reaction anaerobic

A

add vegetable oil to the top and cover the conical flask with a cotton wool bung

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13
Q

When does the fermentation reaction stop?

A

When the concentration of alcohol reaches about 15% to 20% because the yeast gets killed off by the alcohol and can no longer catalyse the reaction

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14
Q

How can you collect a concentrated solution of ethanol

A

Use filtration to collect the dilute ethanol from the conical flask
use fractional distillation to heat the ethanol vapour
use a liebig condenser to condense the vapour and collect the concentrated ethanol liquid

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15
Q

Carboxylic acids functional group

A
  • COOH
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16
Q

what do carboxylic acids end in

A
  • anoic
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17
Q

What type of acids are carboxylic acids?

A

Weak acids : they only partially ionise which means they only sometimes release H+ ions

18
Q

What are polymers?

A

Substance with a high RAM made by joining lots of small repeating units called monomers

19
Q

how are carboxylic acids formed

A

alcohol –oxygen -> carboxylic acids

20
Q

How do alkenes form polymers

A

They open up their double bonds and form bonds with other atoms to form long-chain molecules

21
Q

How do you name polymers

A

Add a poly in front of the monomer and put the monomer in brackets

22
Q

properties of poly(ethene)

A

flexible, electrical insulator, cheap

23
Q

uses of poly(ethene)

A

plastic bags, bottles

24
Q

properties of poly(propene)

A

flexible, strong, mouldable

25
Q

uses of poly(propene)

A

crates, ropes, furniture

26
Q

properties of PVC

A

tough, cheap

27
Q

uses of PVC

A

window frames, water pipes

28
Q

properties of PTFE

A

unreactive, tough, non stick

29
Q

uses of PTFE

A

non- stick pans, waterproof clothing

30
Q

Condensation Polymerisation

A

involves monomers with two different functional groups joining together to create polymer chains

31
Q

how is it different from addition polymerisation

A
  • different functional groups
  • a small molecule (e.g : water ) is lost each time they react
32
Q

ester link

A

formed when dicarboxylic ( 2 carboxylic acid ) and diol ( 2 alcohol ) molecules react ( O=C-O BOND)

33
Q

DNA

A

polymer made up of four different monomers called nucleotides

34
Q

proteins

A

polymers made up of repeating monomers called amino acids

35
Q

Carbohydrates

A

polymers made up of repeating monomers called sugars

36
Q

Raw material of polymers

A

Crude oil

37
Q

Why is the availability of this raw material a problem

A

It is non-renewable which means one day it will run out. The more crude oil we use, the more expensive it becomes due to its increasing scarcity

38
Q

Problems with disposing polymers in landfill sites

A
  • valuable land is quickly used up for landfill sites
  • most polymers are not biodegradable which means they just sit there for millions of years.
    -when it mixes with water it can produce a toxic substance called leachate which can harm the ecosystem
39
Q

Advantages of recycling polymers

A
  • reduces amount of non biodegradable waste in landfills
  • reduces emisions of greenhouse gases by burning polymers
  • uses less resources than making new plastics
  • reduces amount of crude oil needed
  • saves money and creates jobs
40
Q

Disadvantages of recycling polymers

A
  • they must be separated by type before they can be melted and reformed
  • this is difficult and expensive
  • mixed polymers could have reduced quality
  • melting down polymers releases dangerous gases which can harm wildlife
  • can only be done finite amount of times