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A carbonyl compound can be prepared by h...

A carbonyl compound can be prepared by hydration of acetylene. It reacts with ammonia to form (X) and with hydroxylamine to form (Y). It undergoes Wolff-Kishner reduction to form Z. X, Y and Z are

A

Acetaldimine acetaldoxime and ethane

B

Diacetone amine, acetoxime and propane

C

Acetaldoxime , semicarbazone and propane

D

Aldol, hydrazone and alcohol.

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The correct Answer is:
A
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AAKASH SERIES-APPENDICES -REVISION EXERCISE -ALDEHYDES AND KETONES
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  2. Reduction of can be carried out with

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  3. A carbonyl compound can be prepared by hydration of acetylene. It reac...

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  5. Which one of the following is one of the cross end products formed whe...

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  6. X+RMgX rarr Y overset(H(2)O.H^(+))rarr Z . If Z is n-butyl alcohol, ...

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  7. When acetaldehyde undergoes reaction with Zn-HCl in the presence of Hg...

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  8. 2, 3-dimethyl-2-butene, on reductive ozonolysis gives

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  9. HCHO with conc. Alkali forms two compounds. The change in oxidation nu...

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  10. Which of the following compounds would undergo the Cannizaro reaction ...

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  12. Hydrogenation of benzoyl chloride in the presence of Pd and BaSO(4) gi...

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  13. Benzaldehyde is obtained from toluene by

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  14. C(6)H(6) +CO + HCl overset("Anhyd."AlCl(3))rarr X + HCl Compound X is

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  15. In this reaction C(6)H(5)CH(3)underset(CrO(3))overset((CH(3)CO)(2)O)...

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  16. Benzaldehyde undergoes oxidation and reduction in the presence of

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  17. Reaction of C6H5 CHO with CH3NH2 gives

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  18. Schiff's bases are formed when aniline reacts with

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  19. CH(3)CHO and C(6)H(5)CHO can be distinguished by

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  20. Which does not react with Fehling's solution ?

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