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Write the structure and IUPAC name of th...

Write the structure and IUPAC name of the following compounds:
(i) Metylacetylene
(ii) Ethylacetylene
(iii) Dimethylacetylene
(iv) Isopropylmethylacetylene
Strategy: Alkynes are named like the alkenes except for the following two points:
(1). The suffix-yne is added to the characteristic root.
(2). Because the linerar arrangement about the triple bond does not lead to geometric isomerism. the prefixes cis-and itrans-are not used.

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(i) `CH_3--=CH`, propyne
(ii) `CH_3CH_2-C-=CH`, but-1-yne
(iii) `CH_3-C-=C-CH_3` but-2-yne
(iv). `overset(5)(C)H_(3)-underset(CH_(3))underset(|)overset(4)(C)H-overset(3)(C)-=overset(1)(C)H_(3),` 4-emthylpent-2-yne
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R SHARMA-ALKYNES-Archives
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  3. From which one of the following can both ethylene and acetylene be pre...

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  4. The treatment of CH(3)MgX with CH-=CH produces

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  5. The hydrocarbon which can react with sodium in liquid ammonia is

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  6. Base strength of (i) CH3CH2^(-) (ii) CH2=CH^(-) (iii) CH-=C^(-)

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  7. The product C is CH(3).CH(2).C-=CH+HCl rarrBoverset(HI)rarrC

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  8. Under which of the following conditions does the reaction HC-=CH+CH2OH...

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  9. Which of the following reactions will yeild 2,2-dibromo propane?

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  10. The reaction of acetylene and propyne with HgSO4 in the presence of H2...

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  11. An organic compound decolorizes Br2 water and also gives red ppt. with...

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  12. Ethene and ethyne can be distinguished by

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  13. In the following sequency of reactions CH3CH2Broverset(KOH)toXoverse...

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  14. HC-=CH reacts with acetic acid in the presence of Hg^(2g+) ions to giv...

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  15. Aoverset(H(2)//"Lindlar's catalyst")larrCH3C-=C CH(3)overset(Na//Liq" ...

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  16. In the reaction CH3C-=C CH3underset((Zn)/(H2O))overset(R)toCH3COCOCH...

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  17. The products of the following reactions CH3C-=C CH2CH3underset("oxid...

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  18. Propyne when passed through a hot iron tube at 400^@C produces

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  19. H--=-Hoverset((i)O3)underset((ii)(H2O)//(Zn))rarr(A)overset(Zn//CH3COO...

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  20. Which of these will not react with acetylene?

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  21. When CH3CH2CHCl2 is treated with NaNH2, the product formed is

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