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JEE Main 2021
LEVELJEE Main

Animated Solution for Chemistry - Organic Chemistry: The polymer formed on heating novolac with formaldehyde is

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Visualized Solution

\text{Understanding Novolac}

  • Novolac is a linear polymer formed by the condensation of phenol and formaldehyde.
  • It consists of phenol rings linked by groups at the ortho positions.

\text{Reaction with Formaldehyde}

  • When Novolac is heated with additional formaldehyde (), further condensation occurs.
  • Formaldehyde provides the bridges needed for cross-linking.

\text{Formation of Cross-links}

  • The groups connect the para positions of the phenol rings in adjacent Novolac chains.
  • This creates a heavily cross-linked, three-dimensional network.

\text{Bakelite}

  • This infusible, solid mass formed by cross-linking is called \textbf{Bakelite}.
  • Therefore, heating Novolac with formaldehyde yields Bakelite.

\text{Properties and Uses}

  • Bakelite is a \textbf{thermosetting polymer}.
  • It is used for making electrical switches, handles of utensils, and computer discs due to its heat resistance and insulating properties.

The Sigma Insight: Polymers

Solution Diagram
Welcome to the fascinating world of polymers! Today, we are going to dive deep into the chemistry of one of the most historically significant and widely used synthetic plastics: Bakelite.
This isn't just a simple chemical reaction; it's a story of how simple, linear molecules can be transformed into an indestructible, three-dimensional fortress. Let's break down the journey from Novolac to Bakelite.

The Linear Journey

Novolac
Before we can build a fortress, we need the right materials. Our starting material here is Novolac.
Novolac is a linear polymer. Imagine a long, straight chain of beads. In the chemical world, these "beads" are phenol rings, and they are linked together by methylene groups, which we write as . These linkages specifically occur at the ortho positions of the phenol rings.
Because Novolac is linear, its chains can slide past one another when heated. This makes it a thermoplastic material at this stage. But we want something stronger, something that can withstand intense heat without melting.

The Catalyst for Change

Formaldehyde
To transform our linear Novolac into something much more robust, we introduce a cross-linking agent: Formaldehyde ().
When we take Novolac and heat it in the presence of additional formaldehyde, a secondary condensation reaction kicks off. The formaldehyde molecules act like tiny chemical bridges. They seek out the available reactive sites on the phenol rings—specifically, the para positions that were left untouched during the formation of Novolac.

The 3D Transformation

Bakelite
As the heat is applied, the magic happens. The formaldehyde molecules form new bridges, but this time, they don't just extend the chain. They connect one linear Novolac chain to another adjacent chain.
Imagine taking several straight ladders and bolting them together side-by-side. Suddenly, you no longer have individual ladders; you have a massive, rigid scaffolding.
This heavily cross-linked, three-dimensional network is what we call Bakelite.
Because all the chains are now covalently bonded to each other in multiple directions, the molecules can no longer slide past one another. This makes Bakelite an infusible solid mass. It is a classic example of a thermosetting polymer—once it is molded and set into a shape, no amount of heat will melt it again; it will only char or burn.

Why Does This Matter?

Understanding the structure of Bakelite explains its real-world applications. Because of its incredible heat resistance and excellent electrical insulating properties, Bakelite became the material of choice for making electrical switches, plug points, and the handles of cooking utensils.
So, the next time you turn on a light switch or pick up a hot frying pan by its handle, remember the beautiful, cross-linked chemistry of Bakelite that makes it all possible!

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