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A compund X(C8H10O) upon treatment with ...

A compund `X(C_8H_10O)` upon treatment with alkaline solution of iodine gives a yellow precipitate. The filtrate on acidifiction gives a whit solid `Y(C_7H_6O_2)` Write the strctures of X and Y.

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A compound D(C_(8)H_(10)O) upon treatement with alkaline solution of iodine gives a yellow precipitate. The fibtrate on acidification gives a white solid E(C_(7)H_(6)O_(2)) . Write the structures of D,E .

An organic compound (A) (C_(8)H_(8)O_(3)) was insoluble in water, dilute HCI, and NaHCO_(3) . It was soluble in NaOH. A solution of (A) in dilute NaOH was boiled and steam distilled and distillate was reacted with NaOH to give a yellow precipitate. The alkaline residue is acidifield to give a solid (B) (C_(7)H_(6)O_(3)) . (B) dissolves in aqueous NaHCO_(3) with the evolution of gas. Identify (A) and (B).

Compound A,C_(8)H_(10)O , is found to react with NaOI (produced by reacting Y with NaOH ) and yields a yellow precipitate with characteristic smell. A and Y are respectively (a) (b) (c) (d)

An aromatic compound (X) (C_(8)H_(8)O) gives positive 2, 4-DNP test. It gives a yellow precipitate of compound (Y) on reaction with iodine and sodium hydroxide solution. (X) does not give Tollens' test on oxidation under drastic conditions. It gives a carboxylic acid (Z) (C_(7)H_(6)O_(2)) .(Z) is also formed with (Y) during the reaction. (X), (Y) and (Z) respectively are

Compound (X) C_(6)H_(5)O gives yellow coloured ppt with 2,4 DNP but does not give red colored ppt with Fehiling's solution (X) on treatement with NH_(2)OH H^(+) gives compound (Y) C_(6)H_(5)NO (Y) when treated with PCl_(5) gives isomeric compound (Z) . (Z) on hydrolysis gives propanoic acid and aniline. what will be the correct structure of (X) ,(Y) and (Z) ?

X' compound (C_(4)H_(8)O) decolorises bromine water react with I_(2) & NaOH it give yellow ppt identify 'X'

The compound C_8H_9Cl(A) on treatments with KCN followed by hydrolysis gives C_9H_10O_2(B) .Ammonium salt of B on dry distillation yields C.Which reacts with alkaline solution of bromine to gives C_8H_11N .(D)Another compound E is obtained by the action of nitrous acid on D. E on oxidation gives F which gives the inner anhydride G on heating. The Compound A is :

ALLEN-ALKENE, ALKANE & ALKYNE -EXERCISE-5[B]
  1. When t-butanol and n-butanol are separately treated with a few drops o...

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  2. 3,3-dimethylbutan-2-ol losses a molecule of water in the presence of c...

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  3. A compund X(C8H10O) upon treatment with alkaline solution of iodine gi...

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  4. Which of the following is the correct method to synthesise methyl-t-by...

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  5. overset("Conc". H(2)SO(4))rarr(A)

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  6. Write the intermediate steps for the following reactio.

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  7. Explain why o-hydroxy benzaldehyde is a liquid at room temperature whi...

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  8. Write the structure of the product A & B C(2)H(5)-underset(O)underse...

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  9. Cyclobutyl bromide on treatment with magnesium in dry ether forms an o...

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  10. How would you synthesis 4-methoxyphenol form bromobenzene in NOT more ...

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  11. Identify Z + Y in the following synthetic scheme and write their struc...

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  12. Compound (X) on reduction with LiAIH(4) gives a hydride (Y) containin...

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  13. A racemic mixture of (+-) 2-pheynl propanoic acid on esterification wi...

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  14. Write steps to carry out the conversion of phenol to aspirin.

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  15. Convert nitrobenzene to sulphanilic acid in not more than four step...

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  16. (i) An organic compound (P), C5H10O reacts with dil. H2SO4 to give (Q)...

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  17. Identify (X) and (Y).

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  18. When phenyl magnesium bromide reacts with t-butanol the product would ...

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  19. Statement-1:p-Hydroxybenzoic acid has a lower boiling point that o-Hyd...

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  20. In the reaction the product are

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