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Mass of a biodegradable condensation copolymer from glycine and 6-aminohexanoic acid
JEE Advanced 2026
Paper 2 · Question 14
Chemistry
Condensation copolymer from a reaction sequence
Moderate-Hard
Five short screens: charge the reactor, watch CH3I become glycine one reagent at a time, watch caprolactam's ring unroll into 6-aminohexanoic acid, link the two monomers while every condensation ejects a water, assemble the arithmetic - and then reveal the mass of Z in spray-paint lettering.
Open the interactive simulationSub-topics covered
- Nitrile route for one-carbon ascent
- Hydrolysis of a nitrile to a carboxylic acid
- Hell-Volhard-Zelinsky alpha-bromination
- Amination of an alpha-halo acid
- Acidic hydrolysis of a lactam and ring opening
- Condensation polymerisation and the water eliminated
- Linear chain: n units give n minus 1 links
What it teaches
- Cyanide displacement is the only step in the sequence that changes the carbon count, which alone fixes X as a two-carbon acid
- Red P with Br2 is the Hell-Volhard-Zelinsky reaction and brominates the alpha carbon of an acid
- Excess ammonia converts an alpha-bromo acid to an alpha-amino acid without alkylating twice
- A lactam is a cyclic amide; hydrolysis adds a water across the C-N bond and opens the ring, so the product is 18 heavier than the lactam
- A polyamide needs an amine at one end and an acid at the other, which is why both monomers must be acyclic
- Condensation polymerisation ejects one small molecule per link, so the polymer is always lighter than the monomers that made it
- A chain of n units with two loose ends has n minus 1 links, not n - the word acyclic in the question is what makes it 999 rather than 1000
- Not every number given in a question is used: bromine appears only in an intermediate and never reaches the answer
Simulation ID
- ADV-2026-P2-CHE-Q14 · revision 1
See this simulation in the library → · open the simulation file on its own