Chapter 17 (17.1 - 17.3 + 17.7) Polymers Flashcards

1
Q

what are polymers

A

polymers are large molecules linked together with many smaller molecules (monomers)

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2
Q

what are the 2 main links in polymers

A

amide linkage
ester linkage

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3
Q

what are the 2 main types of polymers

A

synthetic
natural

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4
Q

how are synthetic molecules made

A

made by polymerisation (addition or condensation)

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5
Q

how are natural polymers made

A

found in the environment/nature

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6
Q

what is addition polymerisation

A

can happen with only unsaturated hydrocarbons where the double bond breaks to form a polymer. Only one type of monomer to form only one product: the polymer itself.

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7
Q

examples of addition polymerisation

A

ethene —> polyethene
pentene —> polypentene

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8
Q

what is condensation polymerisation

A

condensation polymerisation 2 reactants used and by product is given out

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9
Q

what is the ester linkage

example of 2 monomers that form it

A

-c=o-o

A dicarboxylic acid + A diol

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10
Q

what is the amide linkage

A

-C=O-N-H

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11
Q

which two bio molecules are made from condensation polymerisation and which linkage do they have

A

carbs: glycosidic linkage (-O-)
proteins: amide linkage

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12
Q

what is the main difference between condensation polymerisation and addition

A

Addition polymerisation forms the polymer molecule only
Condensation polymerisation forms the polymer molecule and eliminates another small molecule per linakge

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13
Q

how are the functional groups of polymers made (condensation)

A

The functional groups at the ends of one monomer react with the functional group on the end of the other monomer, in so doing creating long chains of alternating monomers, forming the polymer and giving a by product

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14
Q

how to draw a polymer

A

1) To draw a repeat unit, change the double bond in the monomer to a single bond in the repeat unit
2) Add a bond to each end of the repeat unit
3) The bonds on either side of the polymer must extend outside the brackets (these are called extension or continuation bonds)
4) A small subscript n is written on the bottom right hand side to indicate a large number of repeat units
5) Add on the rest of the groups in the same order that they surrounded the double bond in the monomer

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15
Q

how is nylon formed

A

1)Nylon is a polyamide made from dicarboxylic acid monomers (a carboxylic with a -COOH group at either end) and diamines (an amine with an -NH2 group at either end)
2)Each -COOH group reacts with another -NH2 group on another monomer
3)An amide linkage is formed with the subsequent loss of one water molecule per link

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16
Q

What kinda polymer is PET

A

polyester

17
Q

How can PET be broken down into its monomers again

explain
conditions

A

Hydrolysis - PET is reacted with steam at high temps and pressure

Eliminated water is put back in

18
Q

What are proteins
how are they formed

A

natural polyamides
amino acid monomers join to form proteins

19
Q

(1Describe the general structure of a n amino acid

Functional grps
what is ‘R’

A

1 amine functional grp, 1 carboxyl
functional grp

R represents different types of side chain for the different amino acids

20
Q

State two uses of synthetic polymers.

A

clothes
bowls

21
Q

Name another substance which can hydrolyse proteins. (apart from enzymes)

A

hydrochloric acid / any strong acid / any strong alkali

22
Q

what is the carbohydrate group

A

-o-

23
Q

what is lost in amide linkage making

A

water h2o

24
Q

what is needed for reaction between carboxylic acid and alcohol

A

acid catalyst (conc h2so4)
heat

25
Q

ethanol, C2H6O, is not a carbohydrate but glucose, C6H12O6 is. why?

A

carbohydrates have 2H:1O ratio
contain elements of water

26
Q

Define carbohydrates

A

Contains carbon, hydrogen and oxygen with a ratio of 2H : 1O