
The question asks for the specific reagents used in the synthesis of m‐(n‐Butyl)toluene from n‐propyl m‐tolyl ketone. The reaction involves the conversion of a ketone to a hydrocarbon, which is a reduction process.
In organic chemistry, the Wolff-Kishner reduction is commonly used to reduce ketones to alkanes. The reagents involved in this reduction are hydrazine (\(NH_2NH_2\)) and a strong base, typically NaOH. This reaction proceeds by the formation of a hydrazone intermediate, which upon heating decomposes to form the alkane.
Let's analyze the options:
Based on this analysis, the correct reagent set for the reduction of n‐propyl m‐tolyl ketone to m‐(n‐Butyl)toluene is NH_2NH_2 , NaOH.

List I | List II | ||
|---|---|---|---|
| A | \(\Omega^{-1}\) | I | Specific conductance |
| B | \(∧\) | II | Electrical conductance |
| C | k | III | Specific resistance |
| D | \(\rho\) | IV | Equivalent conductance |
List I | List II | ||
|---|---|---|---|
| A | Constant heat (q = 0) | I | Isothermal |
| B | Reversible process at constant temperature (dT = 0) | II | Isometric |
| C | Constant volume (dV = 0) | III | Adiabatic |
| D | Constant pressure (dP = 0) | IV | Isobar |