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NEET CHEMISTRYHydrocarbonsMedium

Question

Phenylacetylene undergoes a reaction with dilute H2SO4\text{H}_2\text{SO}_4 in the presence of HgSO4\text{HgSO}_4 to yield:

A

Option 1 (Structure missing)

B

Option 2 (Structure missing)

C

Option 3 (Structure missing)

D

Option 4 (Structure missing)

Step-by-Step Solution

Alkynes react with water in the presence of dilute sulphuric acid and mercuric sulphate at 333 K333\text{ K} to undergo a hydration reaction . The addition of water across the triple bond follows Markovnikov's rule. For phenylacetylene (C6H5-CCH\text{C}_6\text{H}_5\text{-C}\equiv\text{CH}), this hydration initially yields an unstable enol intermediate (C6H5-C(OH)=CH2\text{C}_6\text{H}_5\text{-C(OH)=CH}_2), which rapidly undergoes tautomerisation to form the more stable ketone product, acetophenone (C6H5COCH3\text{C}_6\text{H}_5\text{COCH}_3).

Note: The specific chemical structures for the options were missing from the input data. Option 1 is marked correct based on the provided probable answer.

Exam Context & Concepts Covered

This question aligns with the NEET CHEMISTRY syllabus, specifically targeting concepts from Hydrocarbons. Mastering this topic is crucial for scoring well in the upcoming medical entrance examinations. Solving conceptually related problems will help you understand the nuances of these concepts and improve your problem-solving speed.

CHEMISTRYHydrocarbonsphenylacetyleneundergoesreactiondilutetexthtextso

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A.(Option 1 Structure Missing)
B.(Option 2 Structure Missing)
C.4
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