Degradable Polymers (Cambridge (CIE) A Level Chemistry): Exam Questions

Exam code: 9701

33 mins4 questions
1a
1 mark

This question is about hydrolysis of polymers.

What is meant by a hydrolysis reaction?

1b
2 marks

Describe the reaction conditions and state what occurs to the polyester during acid hydrolysis.

1c
2 marks

Outline the difference in the product(s) between acid and base hydrolysis of a polyester.

1d
4 marks

Draw structures for the products of acid and base hydrolysis of the following polymer:

6-6_q3d-ocr-a-as--a-level-easy-sq
1a
3 marks

Nylon is an example of a synthetic polyamide and contains the same links as polypeptides. Nylon is the general name for a family of polyamides. A section of a nylon polymer is shown in Fig. 1.1.

aqa-chemistry-trial-june

Fig. 1.1  

i) Draw the structures of two monomers that could be used to make this nylon. 

[2]

ii) State the type of polymerisation involved in the formation of this nylon. 

[1]

1b
5 marks

Nylon can be used to make clothing. Suggest why nylon should be protected from spillages of strong acids and alkalis.

1c
2 marks

Nomex shown in Fig. 1.2 has a higher melting point than nylon and is used to make the flame resistant body suits worn by racing drivers. 

Suggest a reason why the melting point of Nomex is higher than that of nylon.

10

Fig. 1.2

1d
3 marks

i) Draw the two monomers that are used to manufacture Nomex






 

  [2]

ii) State the formula of any by-products produced. 

[1]

2a
3 marks

i) Name an example of a synthetic polyester and a synthetic polyamide. 

polyester 

[1]

 polyamide 

[1]

 ii) Polyesters and polyamides are formed by condensation reactions. 

Name a molecule which is commonly eliminated in such reactions. 

[1]

2b
2 marks

Table 2.1 shows the repeat units of a number of polymers. Place a tick () against the ones which are biodegradable.

Table 2.1

7-7-4b-m--polymer
2c
2 marks

Draw the structures of two monomers used to form polymer B.

3a
1 mark

A section of polypeptide was hydrolysed and the amino acids in Table 3.1 were identified.

Table 3.1

Amino Acid

Formula

T

CH3CH(NH2)CO2H

U

C6H5CH2CH(NH2)CO2H

V

H2N(CH2)4CH(NH2)CO2H

Which of the amino acids T, U or V has the highest pH in an aqueous solution? Explain your answer.

Amino acid .............................

3b
1 mark

State how many different dipeptides could be formed from a reaction mixture consisting of amino acids T and U.

3c
2 marks

Polypeptides contain a high proportion of carbon and hydrogen in their structures, yet many are soluble in water. By referring to the structure of a polypeptide, explain why.