DP Chemistry (last assessment 2024)

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Question 23M.3.HL.TZ2.4

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Date May 2023 Marks available [Maximum mark: 12] Reference code 23M.3.HL.TZ2.4
Level HL Paper 3 Time zone TZ2
Command term Draw, Explain, Give, Identify, Outline, State Question number 4 Adapted from N/A
4.
[Maximum mark: 12]
23M.3.HL.TZ2.4

Sections of two forms of polystyrene are shown:

(a.i)

Draw the structural formula of the monomer from which they were formed.

[1]

Markscheme

 

Accept “−C6H5“ for phenyl group.

(a.ii)

Identify, giving one reason, the form with the higher melting point.

[1]

Markscheme

B AND chains «of polymer» can align/pack more closely ✓

 

Do not accept “stronger intermolecular forces between chains”.

(b)

Explain how a substance in the same phase as the reactants can reduce the activation energy and act as a catalyst. 

[2]

Markscheme

forms an intermediate/activated complex ✓
«intermediate/activated complex» dissociates to form product «AND catalyst» ✓

 

Accept correct annotated energy profile for either mark.

(c)

Solutions of substituted polystyrenes can form lyotropic liquid crystals. Outline how lyotropic liquid crystals differ from other liquid crystals.

[1]

Markscheme

«lyotropic liquid crystals» exist over a given concentration range AND other liquid crystals exist over a certain temperature range ✓

(d)

Expanded polystyrene (EPS) is a useful material.

(d.i)

Explain how polystyrene is converted to EPS.

[2]

Markscheme

volatile hydrocarbon/pentane «incorporated in beads of the polymer» ✓
vaporizes/boils when heated «causing polymer to expand» ✓

 

Accept names or formulas for M1.

Accept “carbon dioxide” for M1.

(d.ii)

State one property of EPS that makes it a useful material.

[1]

Markscheme

«good» thermal/electrical insulator
OR
soft/provides shock resistance
OR
low density
OR
easily moulded/versatile
OR
water resistant
OR
durable ✓

 

Accept “easy on-site usage”
OR
“environmentally sustainable”
OR
“non-toxic”
OR
«chemically» inert”.

Accept “lightweight” for “low density”.

Nylon-6 is a polymer that can be formed from the monomer:

(e)

State the type of polymerization reaction that occurs and the structural characteristic of the monomer that allows this type of polymerization to occur.

 

Type of polymerization: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  


Structural characteristic: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  

[2]

Markscheme

Type of polymerization: condensation ✓
Structural characteristic: two functional groups ✓

 

Accept “polycondensation” for M1.

(f)

Outline why plastics do not break down easily in the environment.

[1]

Markscheme

strong covalent bonds ✓

 

Accept “close packing of chains”
OR
“hydrophobicity”.

(g)

State the RIC number for polyamide plastic (nylon). Use section 30 of the data booklet.

[1]

Markscheme

«RIC» 7 ✓