Compound X of molecular formula C4H6 takes up one equivalent of hydro...
Compound X:
Compound X has the molecular formula C4H6. To determine its structure, we can start by analyzing the given options and eliminate those that do not fit the molecular formula.
Option A: CH2 = CH - CH = CH2
This compound has four carbon atoms and six hydrogen atoms, matching the molecular formula of X. Therefore, option A is a possible structure for compound X.
Option B: CH2 = C = CHCH3
This compound also has four carbon atoms and six hydrogen atoms, matching the molecular formula of X. Therefore, option B is a possible structure for compound X.
Option C: CH3C ≡ CCH
This compound has five carbon atoms and six hydrogen atoms, not matching the molecular formula of X. Therefore, option C is not a possible structure for compound X.
Compound Y:
Compound Y is formed when compound X reacts with one equivalent of hydrogen in the presence of Pt. This reaction is a typical hydrogenation reaction, where an unsaturated compound gains hydrogen atoms to become saturated.
Ozonolysis:
Ozonolysis is a reaction where an unsaturated compound reacts with ozone (O3) to form smaller organic compounds. In this case, compound Y on ozonolysis gives only ethanoic acid (CH3COOH).
Conclusion:
The only structures that fit the given information are options A and B. Both options have the same molecular formula as compound X (C4H6), and their ozonolysis products would result in ethanoic acid. Therefore, both options A and B are possible structures for compound X.
Correct Answer: Option D (All three options A, B, and C) are possible structures for compound X.
Compound X of molecular formula C4H6 takes up one equivalent of hydro...
Formation of only CH
3COOH by ozonolysis indicate that the compound Y should be CH
3CH = CHCH
3 which can be farmed by all of the three given compounds
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