In gasoline stability, which hydrocarbon family tends to show the highest gum-forming tendency during storage: paraffins, naphthenes, aromatics, or diolefins?

Difficulty: Easy

Correct Answer: Diolefins

Explanation:


Introduction:
Gum formation in gasoline arises from oxidative polymerization of reactive unsaturates. Identifying the hydrocarbon class most prone to forming gums is essential for storage stability and additive selection.

Given Data / Assumptions:

  • Compare gum tendency among paraffins, naphthenes, aromatics, and diolefins.
  • Ambient storage with oxygen exposure is implied.


Concept / Approach:
Reactivity increases with unsaturation: diolefins (dienes) > mono-olefins > aromatics ≈ naphthenes ≈ paraffins (least). Dienes readily oxidize and polymerize, generating gums.

Step-by-Step Solution:

1) Rank families by unsaturation and radical stability.2) Recognize dienes (diolefins) as most reactive for gum formation.3) Select “Diolefins.”


Verification / Alternative check:
ASTM gum tests and textbook trends consistently show highest gum precursors in olefinic—especially diene—fractions.

Why Other Options Are Wrong:

Paraffins: saturated; poor gum formers.Aromatics: relatively stable ring; lower gum tendency than dienes.Naphthenes: saturated cyclics; low gum tendency.


Common Pitfalls:
Assuming high octane (aromatics) implies instability; octane and oxidative stability are distinct properties.


Final Answer:
Diolefins

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