



L-Glucose is the enantiomer of D-Glucose, which means it has the same structure as D-Glucose but with opposite configurations at each chiral center.
In L-Glucose, the -OH groups are positioned in such a way that it is a mirror image of D-Glucose.
For L-Glucose, the configuration of the hydroxyl (-OH) groups should be as follows from top to bottom:
Based on the given configurations, Option (1) matches the structure of L-Glucose.
The correct structure of L-Glucose is represented by Option (1).
A substance 'X' (1.5 g) dissolved in 150 g of a solvent 'Y' (molar mass = 300 g mol$^{-1}$) led to an elevation of the boiling point by 0.5 K. The relative lowering in the vapour pressure of the solvent 'Y' is $____________ \(\times 10^{-2}\). (nearest integer)
[Given : $K_{b}$ of the solvent = 5.0 K kg mol$^{-1}$]
Assume the solution to be dilute and no association or dissociation of X takes place in solution.
Inductance of a coil with \(10^4\) turns is \(10\,\text{mH}\) and it is connected to a DC source of \(10\,\text{V}\) with internal resistance \(10\,\Omega\). The energy density in the inductor when the current reaches \( \left(\frac{1}{e}\right) \) of its maximum value is \[ \alpha \pi \times \frac{1}{e^2}\ \text{J m}^{-3}. \] The value of \( \alpha \) is _________.
\[ (\mu_0 = 4\pi \times 10^{-7}\ \text{TmA}^{-1}) \]