Organic compounds can be distinguished using chemical tests. Table 4.1 shows four pairs of compounds. [Table 4.1 showing pairs A1/A2, B1/B2, C1/C2, D1/D2 with structures]
- (a)Complete Table 4.1 to: • identify a reagent that could distinguish between the compounds in each pair • give the positive result of the chemical test and identify which compound shows this result. Use a different reagent for each test.[8]
- (b)C1 has melting point –94 °C and boiling point +49 °C. Explain these properties by referring to the type of van der Waals' forces between molecules.[2]
- (c)Draw the structure of the cis isomer of C2.[1]
- (d)(i)C2 forms a polymer when heated gently. Identify the type of polymer that forms from C2.[1]
- (d)(ii)Draw one repeat unit of the polymer formed from C2.[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 2022). The mark or mark type is shown in brackets.
- [2] For A1 (ketone) / A2 (primary alcohol): Reagent: K2Cr2O7 OR KMnO4 OR Na; Positive result: A2 make solution turn (orange to) green OR turn colourless OR effervescence (respectively)
- [2] For B1 (methyl ketone) / B2 (ester): Reagent: alkaline I2(aq)/ OR 2,4-DNPH; Positive result: B1 gives yellow/orange ppt OR B1 gives red/yellow/orange ppt (respectively)
- [2] For C1 (alkane) / C2 (alkene): Reagent: Br2(aq); Positive result: C2 turns it (orange to) colourless
- [2] For D1 (diol) / D2 (carboxylic acid): Reagent: Na2CO3 / NaHCO3; Positive result: D2 gives effervescence
- [1] M1 (m.& b.pts are low because) weak intermolecular forces / weak van der Waals
- [1] M2 (only) London / dispersion forces / instantaneous dipole-induced dipole
- [1] {cis-pent-2-ene structure}
- [1] addition
- [1] correct carbon backbone including 'dangling' bonds for ONE repeat unit
- [1] rest of structure correct
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