Compound X (molecular formula, C5H8O) does not react appreciably with Lucas reagent at room temperature but gives a precipitate with ammonical silver nitrate. With excess of MeMgBr, 0.42 g of X gives 224 ml of CH4 at STP. Treatment of X with H2 in presence of Pt catalyst followed by boiling with excess HI, gives n-pentane. Suggest structure for X and write the equation involved.
[IIT, 1992]
Compound ‘X’ Lucas reagent No reaction at room temperature
(Mol. formula C5H8O)
Ammonical AgNO3 Precinitates Excess MeMgBr CH4 (ii) Boil with excess HI (i )H2/Pt n-Pentane
Hence in compound X, five C-atoms are present in straight chain. It gives methane with excess GR, so in it acidic hydrogen is present. It gives precipitate with ammonical AgNO3. Therefore, it must have acidic hydrogen in the form of alkynic group. It does not give any reaction with Lucas reagent therefore, it has p-alcoholic group.
So the basis of above properties,the possible structure of compound X is given as follows:
HC≡C–CH2−CH2−CH2OH (mol. formula C5H8O)
Reaction:
(i) HC≡C–CH2CH2−CH2OH at room temp. Lucas reagent No reaction
(ii) HC≡C–CH2CH2−CH2OH+AgNO3+NH4OH→AgC≡CWhite ppt.−CH2CH2−CH2OH+NH4NO3+H2O
(iii) HC≡C–CH2CH2−CH2OH+2MeMgBr→BrMg–C≡C–CH2CH2−CH2O–MgBr+2CH4
(iv) HC≡C–CH2CH2−CH2OH+2H2⟶PtCH3−CH2−CH2−CH2−CH2OH(−I2,−II2O)Boil HICH3−CH2−CH2−CH2−CH3n-pentane
So the compound ‘X’ is HC≡C–CH2−CH2–CH2OH