Step 1: Identifying the Carbonyl Compound X - Given that oxidation of \( X \) gives a carboxylic acid (\( C_3H_6O_2 \)),
- This suggests that \( X \) must be a ketone or aldehyde that can be oxidized to a carboxylic acid.
Step 2: Checking Possible Structures - The simplest possible ketone or aldehyde with \( C_3H_6O \) is propanal or propanone.
- Since oxidation leads to a single carboxylic acid, the compound must be propanal (CH\(_3\)-CH\(_2\)-CHO).
Step 3: Identifying the Oxime of X
- The oxime is formed when aldehydes react with hydroxylamine (NH\(_2\)OH).
- This results in the formation of propanal oxime (CH\(_3\)-CH\(_2\)-CH=NOH).
0.01 mole of an organic compound (X) containing 10% hydrogen, on complete combustion, produced 0.9 g H₂O. Molar mass of (X) is ___________g mol\(^{-1}\).
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 \( 4.606 \times 10^{-2} \text{ s}^{-1} \).
Let $E_1$ and $E_2$ be two independent events of a random experiment such that
$P(E_1) = \frac{1}{2}, \quad P(E_1 \cup E_2) = \frac{2}{3}$.
Then match the items of List-I with the items of List-II:
The correct match is: