Step 1: Understanding the Reaction
- Urea (\( NH_2CONH_2 \)) hydrolyzes in the presence of water to form carbamic acid (\( NH_2COOH \)), which is unstable and decomposes into ammonia (\( NH_3 \)) and carbonic acid (\( H_2CO_3 \)).
- Here, X = Carbamic acid (\( NH_2COOH \)) and Y = Carbon dioxide (\( CO_2 \)).
Step 2: Determining Hybridization of Carbon in \( X \) and \( Y \)
- Carbamic acid (\( NH_2COOH \)) contains a carbonyl (\( C=O \)) functional group, where the carbon is sp\(^2\)-hybridized due to one double bond and two single bonds.
- Carbon dioxide (\( CO_2 \)) has a linear structure with two double bonds, making the carbon sp-hybridized.
Step 3: Identifying the Correct Option
- \( X = NH_2COOH \) → Carbon is \( sp^2 \)-hybridized.
- \( Y = CO_2 \) → Carbon is \( sp \)-hybridized.
- This corresponds to Option (1): \( sp^2, sp \). ✅
From the given following (A to D) cyclic structures, those which will not react with Tollen's reagent are : 
Compound 'P' undergoes the following sequence of reactions : (i) NH₃ (ii) $\Delta$ $\rightarrow$ Q (i) KOH, Br₂ (ii) CHCl₃, KOH (alc), $\Delta$ $\rightarrow$ NC-CH₃. 'P' is : 
