N,N-diethylbenzenesulphonamide does not contain any hydrogen atom attached to nitrogen, making it non-acidic and thus insoluble in alkali.
Step 1: Understanding the Nature of N,N-Diethylbenzenesulphonamide - In order for a compound to dissolve in alkali, it must have an acidic hydrogen atom that can react with OH\(^-\).
Step 2: Why It Is Insoluble - Sulphonamides that contain a hydrogen attached to nitrogen are acidic and dissolve in alkali. - However, in N,N-diethylbenzenesulphonamide, both hydrogen atoms on nitrogen are replaced by ethyl groups, making it non-acidic and hence, insoluble in alkali.
Consider the following two reactions A and B: 
The numerical value of [molar mass of $x$ + molar mass of $y$] is ___.
Which one of the following graphs accurately represents the plot of partial pressure of CS₂ vs its mole fraction in a mixture of acetone and CS₂ at constant temperature?

Consider the following reaction sequence: 
Given: Compound (x) has percentage composition \(76.6%\ \text{C}\), \(6.38%\ \text{H}\) and vapour density \(=47\). Compound (y) develops a characteristic colour with neutral \(\mathrm{FeCl_3}\) solution. Identify the {INCORRECT statement.}
