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We have the reducing agent lithium aluminium hydride whose formula is written as $$\text{LiAlH}_4$$. In this salt the aluminium-centred anion $$\text{AlH}_4^-$$ supplies hydride ions $$\text{H}^-$$ very readily.
Silicon tetrachloride is $$\text{SiCl}_4$$. Whenever a covalent chloride such as $$\text{SiCl}_4$$ is treated with a strong hydride donor, each $$\text{Cl}$$ atom can in principle be replaced by a hydride ion, because the hydride has a very high affinity for the electropositive silicon centre.
First we state the general hydride-transfer idea:
$$\text{SiCl}_4 + 4\,\text{H}^- \longrightarrow \text{SiH}_4 + 4\,\text{Cl}^-$$
Those four chloride ions set free in the process cannot remain free in the reaction mixture; they immediately combine with the available metal cations. There are two different cations present after the hydride has been delivered:
The chloride ions distribute themselves between these two cations according to their charges. One chloride ion pairs with each lithium ion to give lithium chloride:
$$\text{Li}^+ + \text{Cl}^- \longrightarrow \text{LiCl}$$
and three chloride ions bind to each newly formed $$\text{Al}^{3+}$$ to give aluminium trichloride:
$$\text{Al}^{3+} + 3\,\text{Cl}^- \longrightarrow \text{AlCl}_3$$
Putting all the pieces together, a convenient schematic equation is
$$4\,\text{LiAlH}_4 + \text{SiCl}_4 \;\longrightarrow\; \text{SiH}_4 + 4\,\text{LiCl} + 4\,\text{AlCl}_3$$
(The exact stoichiometric coefficients are not asked in the problem; the essential point is simply the identity of the products.) We see clearly that the reaction gives three distinct substances: $$\text{LiCl}$$, $$\text{AlCl}_3$$ and $$\text{SiH}_4$$.
Comparing this product set with the choices provided, only Option B contains the trio $$\text{LiCl}$$, $$\text{AlCl}_3$$ and $$\text{SiH}_4$$.
Hence, the correct answer is Option B.
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