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 (CH3)2SiCl2. 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 (-OH) groups from the water molecules.
This initial step produces an intermediate compound known as a silanediol, specifically dimethylsilanediol, (CH3)2Si(OH)2, along with hydrochloric acid (HCl) 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 X 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:
4(CH3)2SiCl2+4H2O→[(CH3)2SiO]4+8HCl
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, (CH3)2SiCl2:
M=2(12)+6(1)+28+2(35.5)=129 g/mol
We are given 516 g of the reactant. To find the number of moles (n), we divide the given mass by the molar mass:
Looking back at our balanced overall equation, we see a beautiful stoichiometric relationship: exactly 4 moles of dimethyldichlorosilane are required to produce 1 mole of the tetrameric cyclic product X. Therefore, our reaction will theoretically yield exactly 1 mole of X.
Calculating the Final Yield
To find the theoretical mass of the product, we need the molar mass of X, which has the formula [(CH3)2SiO]4.
The mass of a single repeating unit, (CH3)2SiO, is:
Munit=2(12)+6(1)+28+16=74 g/mol
Since it is a tetramer, we multiply this by four:
So, our theoretical yield is 296 g. However, chemical reactions in the real world are rarely perfectly efficient. The problem states that the reaction has a 75% yield.
To find the actual weight of X obtained, we simply take 75% of our theoretical yield:
Wactual=296×10075=296×43=222 g
And there we have it! The final weight of the cyclic product obtained is 222 g.