The Wolff-Kishner reduction is a method used to reduce carbonyl compounds (aldehydes and ketones) to methylene groups (\(-{CH2}-\)) using hydrazine (\({NH2NH2}\)) and a strong base like potassium hydroxide (\({KOH}\)).
General Reaction:
\[ {R-CHO} \xrightarrow[{KOH}]{{NH2NH2}} {R-CH3} \]
This reaction effectively removes the oxygen of the carbonyl group and replaces it with two hydrogen atoms, converting aldehydes/ketones to alkanes.
The decarboxylation reaction involves the loss of a carbon dioxide molecule (\({CO2}\)) from a carboxylic acid, resulting in the formation of a corresponding hydrocarbon.
General Reaction:
\[ {R-COOH} \xrightarrow{\text{heat}} {R-H} + {CO2} \]
This reaction typically occurs upon heating and is often catalyzed by soda lime or mineral acids.
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 \( 4.606 \times 10^{-2} \text{ s}^{-1} \).
A hydrocarbon which does not belong to the same homologous series of carbon compounds is
Time (Hours) | [A] (M) |
---|---|
0 | 0.40 |
1 | 0.20 |
2 | 0.10 |
3 | 0.05 |