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Animated Solution for Chemistry - s and p-Block Elements: The stoichiometric reaction of of dimethyldichlorosilane with water results in a tetrameric cyclic product in yield. The weight (in g) of obtained is_______. [Use, molar mass (): ]

Enter Numerical Value:

Visualized Solution

  • Reactant: Dimethyldichlorosilane,
  • Hydrolysis reaction replaces chlorine atoms with hydroxyl groups to form an intermediate silanediol.

  • The intermediate undergoes condensation.
  • Formation of tetrameric cyclic product .

  • Overall reaction:
  • Molar mass of is .

  • Given mass of
  • Moles of reactant () is calculated by dividing given mass by molar mass.

  • From stoichiometry, of reactant produce of .
  • Molar mass of , is .
  • Theoretical mass of

  • Percentage yield =
  • Actual weight of obtained is of the theoretical yield.

  • Key Takeaway: Hydrolysis of dialkyldichlorosilanes leads to linear or cyclic silicones.
  • Food for thought: What would be the product if we used trimethylchlorosilane, , instead?

The Sigma Insight: Group 14 Elements

Solution Diagram

The Chemistry of Silicones

Welcome to a fascinating journey into the world of inorganic polymers! Silicones are incredibly versatile materials, and their synthesis is a classic topic in JEE Advanced Chemistry. In this problem, we are tasked with finding the actual yield of a cyclic silicone product formed from the hydrolysis of dimethyldichlorosilane.
Let's break down the chemistry step-by-step. We start with our reactant, dimethyldichlorosilane, which has the chemical formula . When this molecule is exposed to water, it undergoes a rapid hydrolysis reaction. The highly electronegative chlorine atoms are excellent leaving groups, and they are replaced by hydroxyl () groups from the water molecules.
This initial step produces an intermediate compound known as a silanediol, specifically dimethylsilanediol, , along with hydrochloric acid () as a byproduct.

The Condensation Phase

Now, silanediols are notoriously unstable and highly reactive. They do not simply remain in solution; instead, they undergo a process called condensation polymerization. In a condensation reaction, molecules join together while losing a small molecule—in this case, water.
Depending on the exact reaction conditions (like temperature, concentration, and solvent), these silanediols can link up to form long, linear polymer chains, or they can bite their own tails to form cyclic structures.
The problem explicitly states that a tetrameric cyclic product is formed. This means exactly four molecules of dimethylsilanediol condense together, releasing four molecules of water, to form an eight-membered ring consisting of alternating silicon and oxygen atoms.
The overall stoichiometric equation for this transformation is:

Crunching the Numbers

With the chemistry understood, we can now move on to the stoichiometry. First, we need to determine how many moles of our starting material we have.
Let's calculate the molar mass of dimethyldichlorosilane, :
We are given of the reactant. To find the number of moles (), we divide the given mass by the molar mass:
Looking back at our balanced overall equation, we see a beautiful stoichiometric relationship: exactly of dimethyldichlorosilane are required to produce of the tetrameric cyclic product . Therefore, our reaction will theoretically yield exactly of .

Calculating the Final Yield

To find the theoretical mass of the product, we need the molar mass of , which has the formula .
The mass of a single repeating unit, , is:
Since it is a tetramer, we multiply this by four:
So, our theoretical yield is . However, chemical reactions in the real world are rarely perfectly efficient. The problem states that the reaction has a yield.
To find the actual weight of obtained, we simply take of our theoretical yield:
And there we have it! The final weight of the cyclic product obtained is .

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