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Identity A,B and C in the following reac...

Identity A,B and C in the following reaction
`HC-=CH underset(HgSO_(4)) overset(dil.H_(2)SO_(4))toA overset(dil.NaOH)toB overset(heat)toC`

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To identify the compounds A, B, and C in the given reaction sequence, let's break down the steps involved in the reaction. ### Step 1: Reaction of Acetylene with Dilute H2SO4 and HgSO4 The reaction starts with acetylene (HC≡CH) reacting with dilute sulfuric acid (H2SO4) in the presence of mercuric sulfate (HgSO4). This reaction leads to the formation of an enol, which is an intermediate compound. **Intermediate A:** - The reaction of acetylene with dilute H2SO4 and HgSO4 results in the formation of **vinyl alcohol (enol)**, which can be represented as: \[ ...
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PRADEEP-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS -CONCEPTUAL QUESTIONS
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  4. Explain why aldehydes are more reactive than ketones.

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  7. Explain, why o-hydroxybenzaldehyde is a liquid at room temperature whi...

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  8. Identity A,B and C in the following reaction HC-=CH underset(HgSO(4)...

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  9. Suggest a suitable oxidising agent for the given conversion. (CH(3))...

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  10. Write the structures (A) to (C) for the following reactions: .

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  11. An organic compound (A) having moleclar formula C(2)H(6)O on oxidation...

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  13. Fluorine is more electronegative than chlorine but p-fluorobenzoic aci...

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  14. p-Nitrobenzoic acid has higher K(a) value than benzoic acid. Give reas...

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  15. Carboxylic acids donot give the characteristic reactions of carbonyl g...

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  16. Predict the product of the following reaction

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  17. Identify A to E in the following reaction

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  18. Identify A to E in the following series of reactions:

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  19. Write the structure of A,B,C,D and E in the following reactions:

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