If \(A_2B \;\text{is} \;30\%\) ionised in an aqueous solution, then the value of van’t Hoff factor \( i \) is:
To find the van’t Hoff factor (\(i\)) for the compound \(A_2B\) which is 30% ionised, we need to understand how ionisation impacts \(i\).
Assume initially we have 1 mole of \(A_2B\). Upon ionisation, it dissociates as follows:
\(A_2B \rightarrow 2A^+ + B^-\)
This means, for complete ionisation, from 1 mole of \(A_2B\), we would get 2 moles of \(A^+\) and 1 mole of \(B^-\), equating to 3 moles of ions in total.
However, it is only 30% ionised. Therefore:
From 0.3 moles of \(A_2B\) ionised, ions produced are:
Total moles after ionisation = moles undissociated + moles of ions = 0.7 + 0.6 + 0.3 = 1.6 moles
The van’t Hoff factor (\(i\)) is defined as:
\(i = \frac{\text{total moles after ionisation}}{\text{initial moles of solute}} = \frac{1.6}{1} = 1.6\)
The cause for deviation from Raoult’s law in the colligative properties of non-ideal solutions lies in the nature of interactions at the molecular level. These properties show deviations from Raoult’s law due to difference in interactions between solute–solvent, solute–solute and solvent–solvent. Some liquids on mixing form azeotropes which are binary mixtures having the same composition in liquid and vapour phase and boil at a constant temperature. In such cases, it is not possible to separate the components by fractional distillation. There are two types of azeotropes called minimum boiling azeotrope and maximum boiling azeotrope. (a) Pure ethanol cannot be prepared by fractional distillation of ethanol–water mixture. Comment.
The largest $ n \in \mathbb{N} $ such that $ 3^n $ divides 50! is:
The term independent of $ x $ in the expansion of $$ \left( \frac{x + 1}{x^{3/2} + 1 - \sqrt{x}} \cdot \frac{x + 1}{x - \sqrt{x}} \right)^{10} $$ for $ x>1 $ is: