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Q. Statement 1: Acetylene on reacting with sodamide gives sodium acetylide and ammonia.
Statement 2: $sp$-hybridised carbon atoms of acetylene are considerably electronegative.

Hydrocarbons

Solution:

Acetylene on reaction with sodamide gives sodium acetylide and ammonia.
$CH \equiv CH \xrightarrow{NaNH_2} \underset{\overset{\text{monosodium}}{\text{acetylide}}}{CH \equiv \overset{-}{C}\overset{+}{Na}} + NH_3$
Here formation of sodium acetylide can be explained by $sp$ hydridisation of carbon atom. As we know that an electron in $s$-orbital is more tightly held than in a $p$-orbital. In $sp$ hydridisation, $5$-character is $50\%$ as compared to $sp^2 (33\%)$ or $sp^3 (25\%)$. So, due to large s-character the carbon atom is quite electronegative and hence $Na$ of $NaNH_2$ can replace $H^+$ of $C - H$ bond.
Hence statement $1$ and statement $2$ both are true and statement $2$ is the correct explanation of statement $1$.