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How will you prepare (i) cis-pent-2-ene ...

How will you prepare (i) cis-pent-2-ene and trans-pent-2-ene by starting with ethyne ?

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To prepare cis-pent-2-ene and trans-pent-2-ene starting from ethyne, we can follow these steps: ### Step 1: Formation of Ethyne Start with ethyne (C2H2), which is represented as H-C≡C-H. ### Step 2: Deprotonation to Form Dianion React ethyne with sodium amide (NaNH2). The sodium amide acts as a strong base and removes two protons (H+) from ethyne, resulting in the formation of the ethyne dianion (C2H2^2-). ...
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PRADEEP-HYDROCARBONS-CONCEPTUAL Questions
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  2. Is it possible to isolate pure staggered ethane or pure eclipsed ethan...

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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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