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.
For the thermal decomposition of \( N_2O_5(g) \) at constant volume, the following table can be formed, for the reaction mentioned below: \[ 2 N_2O_5(g) \rightarrow 2 N_2O_4(g) + O_2(g) \] Given: Rate constant for the reaction is \( 4.606 \times 10^{-2} \text{ s}^{-1} \).
“One of these days you’re going to talk yourself into a load of trouble,” her father said aggressively. What do you learn about Sophie’s father from these lines? (Going Places)