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Natural polymers: hydrolyse, then find the monomers sim

Heat a protein with acid, take samples over time and run them beside known amino acids. Spray the dried paper, measure the Rf values of the spots that appear, and see why early samples show fewer. Then join amino acids into a chain and count the water given off.

Natural polymers: hydrolysing proteins and starch, and identifying the monomers by chromatography · covers the GCSE (Higher), IGCSE (Supplement), O-Level (Rf and locating agents only) topic

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What the sim shows

Proteins and starch are natural polymers. A protein is a polyamide: amino acids joined by peptide (amide) links, -CONH-, each made by condensation, with one water given off per link. Heating the protein under reflux with hydrochloric acid hydrolyses those links (water is added back) and sets the amino acids free; starch is hydrolysed by acid right down to glucose (maltose on the way) or by the enzyme amylase (which stops mostly at maltose). Amino acids and sugars are colourless, so the dried chromatogram is sprayed with a locating agent that makes the spots show. Rf = distance moved by the spot / distance moved by the solvent front, both from the pencil line; a spot at the same Rf as a known amino acid in the same solvent is that amino acid. A sample taken before heating shows nothing; for the protein, early samples show fewer spots than later ones, because the hydrolysis is not finished. The paper and solvent follow the library's chromatography figure: the paper is wet √(0.09 × time) up from the solvent, which sits 0.5 cm below the pencil line. Model limits: the Rf values are examples for one solvent; how fast each amino acid is set free, and the least that shows as a spot, are illustrative; gelatin holds many more amino acids than the four shown; you do not need to know the name of any locating agent.

  • Reflux: the flask on a heating mantle, condenser on top
  • Standards, paper on a tile, tank with solvent
  • Spray: a locating agent shows colourless spots

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