When acetic acid is treated with phosphorus pentoxide (\(P_4O_{10}\)), a dehydrating agent, it forms acetic anhydride:
\[ 2{CH3COOH} \xrightarrow{P_4O_{10}} ({CH3CO})_2{O} \]
Phenyl chloride (\({C6H5CCl}\)) reacts with dimethyl cadmium (\(({CH3})_2{Cd}\)) to form a methylated aromatic compound. This typically results in the formation of acetophenone (\({C6H5COCH3}\)) or a related methylated derivative, depending on the conditions.
On strong heating, a benzoyl compound or related acid derivative can undergo conversion to an amide. The resulting product is benzamide:
\[ {C6H5CONH2} \]
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 |