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Starting with ethyne, how will you prep...

Starting with ethyne, how will
you prepare pentan-2-one ?

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To prepare pentan-2-one starting from ethyne, we can follow these steps: ### Step 1: Formation of a Nucleophile Start with ethyne (HC≡CH). Treat ethyne with sodium amide (NaNH2) to generate a nucleophile. The reaction will deprotonate ethyne to form the acetylide ion (HC≡C⁻). **Reaction:** \[ \text{HC≡CH} + \text{NaNH}_2 \rightarrow \text{HC≡C}^- \text{Na}^+ + \text{NH}_3 \] ...
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PRADEEP-HYDROCARBONS-CONCEPTUAL Questions
  1. a. Why are alkanes inert ? b. Why the (C----C) bond rather than (C...

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  2. Is it possible to isolate pure staggered ethane or pure eclipsed ethan...

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  3. Dehydration of alcohol to form an alkene is always carried out with co...

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  4. Dehydration of 1-butanol or 2-butanol with conc. H2SO4 always gives th...

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  5. Predict the major product of the following reaction: C(6)H(6)+(CH(3))(...

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  6. Identify the organic products obtained in the following reaction :

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  7. Predict the products of the following reaction

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  8. Complete the following reactions with appropriate structures of produc...

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  9. How will you prepare 3-methylbut-1-yne by starting with ethyne ?

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  10. Predict the major product in the following reaction : R-C-=C-R under...

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  11. Identify the product in the reaction PhC-=CMe overset(H3O^(+),Hg^(2+)?...

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  12. How will you prepare (i) cis-pent-2-ene and trans-pent-2-ene by starti...

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  13. Starting with ethyne, how will you prepare pentan-2-one ?

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  14. How will you separate a mixture of ethane, ethylene and acetylene ?

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  15. Give reasons for the following: CH2=CH^(Θ) is more basic than HC-=C^...

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  16. Predict which of the following systems would be aromatic and why ?

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  17. Ozonolysis of mesitylene gives

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  18. Write the major product in each case

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  19. Tert-Butylbenzene does not benzoic acid on oxidation with acidic KMnO(...

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  20. How will you explain the directive influence of (i)-CH=CH2 and (ii...

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