To determine the strongest reducing agent among the given hydrides—\( \text{NH}_3 \), \( \text{SbH}_3 \), \( \text{BiH}_3 \), and \( \text{PH}_3 \)—we need to consider their chemical properties, particularly their reducing abilities.
The reducing ability of a hydride depends on the ease with which it can donate electrons to other substances. This ability is influenced by the bond strength between hydrogen and the central atom in the hydride, with weaker bonds leading to stronger reducing agents.
Thus, the correct answer is \(\text{BiH}_3\), which is the strongest reducing agent among the given options.
The reducing strength of hydrides of Group 15 elements increases as we move down the group. This trend can be explained based on the following factors: - As we move down the group, the size of the central atom increases, which weakens the E − H bond (where E is the central atom.) The bond dissociation energy decreases. This makes it easier for the hydride to donate hydrogen (as H$^-$), thereby increasing its reducing power. Among the given options:
NH$_3$ (ammonia) has the strongest N--H bond and, therefore, is the weakest reducing agent.
PH$_3$, SbH$_3$, and BiH$_3$ follow the trend of increasing reducing strength due to weaker bonds as we move down the group.
BiH$_3$ (bismuthine) has the weakest Bi--H bond, making it the strongest reducing agent among the given hydrides.
Conclusion: The strongest reducing agent is BiH$_3$.
Statement-1: \( \text{ClF}_3 \) has 3 possible structures.
Statement-2: \( \text{III} \) is the most stable structure due to least lone pair-bond pair (lp-bp) repulsion.

Which of the following options is correct?