Step 1: Recall glycolysis of PET.
- Glycolysis is a chemical recycling method in which polyesters (like PET) are broken down in the presence of glycols (commonly ethylene glycol).
- This depolymerization produces bis-hydroxyethyl terephthalate (BHET) as the main product.
Step 2: Analyze the given structure.
- The compound shown has:
- A benzene ring with two ester linkages at para positions.
- Each ester is connected to a \(-CH_2CH_2OH\) group.
- This is the typical structure of bis(2-hydroxyethyl) terephthalate, i.e. BHET.
Step 3: Match with polymer precursors.
- PET (Polyethylene terephthalate) is synthesized by condensation of terephthalic acid (or dimethyl terephthalate) with ethylene glycol.
- During glycolysis, PET is broken back into its monomeric unit BHET.
- Thus, the observed compound clearly comes from PET.
Step 4: Eliminate incorrect options.
- (B) Polystyrene → contains styrene monomers (aromatic vinyl group), unrelated.
- (C) Acrylonitrile butadiene styrene → a copolymer, no terephthalate ester units.
- (D) Poly(vinyl chloride) → contains C–Cl bonds, no esters.
- (A) PET → contains terephthalate ester units, matches perfectly.
Final Answer:
\[
\boxed{\text{(A) Poly(ethylene terephthalate)}}
\]