Difficulty: Easy
Correct Answer: It is an isomer of natural rubber (trans-1,4-polyisoprene).
Explanation:
Introduction / Context:
Natural rubber is predominantly cis-1,4-polyisoprene, conferring high elasticity and tack at room temperature. Gutta-percha is trans-1,4-polyisoprene—a stereochemical isomer with very different properties. Distinguishing these forms illustrates how stereochemistry governs polymer mechanics and thermal behaviour.
Given Data / Assumptions:
Concept / Approach:
Trans-1,4-polyisoprene chains pack more efficiently, increasing crystallinity and rigidity; therefore, gutta-percha is relatively hard and non-tacky at ambient conditions. This contrasts with cis-1,4-polyisoprene’s elastomeric character. The key relationship is isomerism, not copolymerisation or thermosetting chemistry.
Step-by-Step Solution:
Identify structural difference: cis vs. trans stereochemistry.Relate trans configuration to increased crystallinity and hardness.Conclude that gutta-percha is an isomer of natural rubber (trans-1,4-polyisoprene).
Verification / Alternative check:
Physical property tables list higher hardness and lower elasticity for gutta-percha than for natural rubber at room temperature.
Why Other Options Are Wrong:
Soft and tacky: describes cis rubber, not gutta-percha.Thermosetting resin: incorrect; gutta-percha is a thermoplastic isomer unless vulcanised.Recovered by coagulation of rubber latex: a general statement for natural rubber production; gutta-percha sources and processing differ.Copolymer with styrene: incorrect; gutta-percha is a homopolymer of isoprene.
Common Pitfalls:
Assuming all “rubbers” are elastomeric at room temperature; stereochemistry can produce hard, crystalline variants.
Final Answer:
It is an isomer of natural rubber (trans-1,4-polyisoprene).
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