Animated Solution for Chemistry - Organic Chemistry: Monomer of novolac is
Select Answer:
Visualized Solution
Origin of Novolac
Novolac is a linear condensation polymer.
Reactants: Phenol and Formaldehyde.
Electrophilic Substitution
Phenol+FormaldehydeH+ or OH−Hydroxymethyl phenols
The Monomer Unit
For linear Novolac, the primary monomer is:
o-hydroxymethylphenol
Structure Analysis
Phenol ring with −CH2OH at ortho position.
Conclusion
Correct Option: (c) o-hydroxymethylphenol
Beyond Novolac
Heating Novolac with more formaldehyde yields Bakelite.
Bakelite is a cross-linked thermosetting polymer.
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The Sigma Insight: Polymers
Solution Diagram
The World of Polymers
Welcome to the fascinating world of polymers! When we look around, from the plastics we use daily to the complex proteins in our bodies, polymers are everywhere. In the realm of synthetic polymers, phenol-formaldehyde resins hold a special place of historical and industrial significance.
Today, we are going to unravel the mystery behind one such important polymer: Novolac. The question asks us to identify the monomer of Novolac. To do this, we need to trace its chemical origins.
The Birth of Novolac
Imagine a reaction flask where we mix phenol and formaldehyde. When we add a little bit of acid or base as a catalyst, a beautiful chemical dance begins. This reaction is a classic example of electrophilic aromatic substitution.
The formaldehyde molecule, acting as an electrophile, attacks the electron-rich ortho and para positions of the phenol ring. This initial attack doesn't immediately give us a giant polymer. Instead, it forms intermediate compounds known as hydroxymethyl phenols.
Phenol+FormaldehydeH+ or OH−o-hydroxymethylphenol+p-hydroxymethylphenol
Identifying the Monomer
Now, here is where the story of Novolac specifically takes shape. Novolac is known to be a linear polymer. For a polymer chain to grow linearly without branching out into a complex 3D web, the polymerization must primarily proceed through one specific type of linkage.
In the case of Novolac, the linear chain is formed by the continuous condensation of the ortho-substituted product. The molecules link together, eliminating water molecules in the process, to form methylene bridges (−CH2−) between the phenol rings.
Therefore, the fundamental building block—the monomer—that repeats to form this linear chain is o-hydroxymethylphenol.
The Final Verdict
Looking at our options, we can easily spot our hero. Option (c) is exactly what we derived: o-hydroxymethylphenol.
Correct Option: (c)
Bonus Insight: If you were to take this linear Novolac and heat it with even more formaldehyde, it would undergo extensive cross-linking, utilizing the para positions as well. This transforms the thermoplastic Novolac into a rigid, infusible, thermosetting plastic known as Bakelite. Always keep this bigger picture in mind!