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प्रश्न
Complete the synthesis by giving missing starting material, reagent or product.

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उत्तर

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संबंधित प्रश्न
A and B are two functional isomers of compound C3H6O.On heating with NaOH and I2, isomer B forms yellow precipitate of iodoform whereas isomer A does not form any precipitate. Write the formulae of A and B.
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An organic compound contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollens’ reagent but forms an addition compound with sodium hydrogensulphite and give positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acid. Write the possible structure of the compound.
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Which sugar does not reduce Fehling's solution?
Acetaldehyde cannot show?
Ammonical silver nitrate solution is called
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The major products formed in the following reaction sequence A and B are:

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The correct set of products obtained in the following reactions:
- \[\ce{RCN ->[reduction]}\]
- \[\ce{RCN ->[(i) CH3MgBr][(ii) H2O]}\]
- \[\ce{RNC ->[hydrolysis]}\]
- \[\ce{RNH2 ->[HNO2]}\]
Choose the reaction which is not possible:
In Tollen's test for aldehyde, the overall number of electrons(s) transferred to the Tollen's reagent formula \[\ce{[Ag(NH3)2]+}\] per aldehyde group to form silver mirror is ______. (Round off to the nearest integer)
Benzaldehyde is obtained from Rosenmund’s reduction of:
Match List-I with List-II:
| List-I (Reaction) |
List-II (Reagents/Condition) |
||
| A. | ![]() |
I. | ![]() |
| B. | ![]() |
II. | CrO3 |
| C. | ![]() |
III. | KMnO4/KOH, Δ |
| D. | ![]() |
IV. | (i) O3 (ii) Zn-H2O |
Choose the correct answer from the options given below:
Fehling’s solution ‘A’ is ______.





