Polyhydroxyamide is a fire-resistant polyamide which is formed from the two monomers, F and G. [Structure of F: HO₂C-C₆H₄-CO₂H (benzene-1,4-dicarboxylic acid)] [Structure of G: H₂N-C₆H₄-OH (4-aminophenol)] Addition polymers can be classified into two types. • homopolymer - a polymer made up of the same monomer unit • copolymer - a polymer made up of two or more different monomer units The reaction of propene, CH3CH=CH2, with phenylethene, C6H5CH=CH2, gives a copolymer.
- (a)(i)Predict the number of peaks that will be seen in the carbon-13 NMR spectra of F and G. number of peaks F | G | [2][2]
- (a)(ii)Draw the repeat unit of polyhydroxyamide. The amide bond should be shown displayed. [2][2]
- (b)When poly(ethene) is formed from ethene, many bonds are broken and formed. Place one tick (✔) in each row of the table to indicate the types of bonds broken and formed in this process. | σ-bonds only | π-bonds only | both σ- and π-bonds bonds broken | bonds formed | [2][2]
- (c)Draw a length of the chain of this copolymer that contains one molecule of each monomer. [2][2]
- (d)(i)Polyalkenes biodegrade very slowly. Explain why by referring to the structures of the polymers. [1][1]
- (d)(ii)Some polymers will degrade in the environment. Describe two processes by which this occurs. 1 ...................................................................................................................................................................................................................... 2 ...................................................................................................................................................................................................................... [2][2]
This question uses a diagram from the original paper, which isn't shown here. Open the full paper from the past papers archive to see it.
Mark scheme
Marking points from the official mark scheme (Oct/Nov 2018). The mark or mark type is shown in brackets.
- [1] for each correct answer
- F: 3
- G: 6
- [1] M1 amide bond displayed
- [1] M2 rest of the structure one repeat unit only
- [1] for each correct tick
- bonds broken: π-bonds only (✔)
- bonds formed: σ-bonds only (✔)
- [1] M1 length of chain with both monomers
- [1] M2 continuation bonds
- [1] C-C bonds are non-polar / have no dipole so cannot be hydrolysed
- [1] M1 Hydrolysis using acid / base / alkali / enzymes
- [1] M2 action of UV light
Write your answer and get it marked
On Oracle Prep you can write or photograph your own answer and have it marked by AI against this mark scheme, with feedback on what you missed.
Sign up free →