Advertisements
Advertisements
प्रश्न
You are given four organic compounds “A”, “B” , “C” and “D”. The compounds “A”, “B” and “C” form an orange-red precipitate with 2, 4 DNP reagent. Compounds “A” and “B” reduce Tollen’s reagent while compounds “C” and “D” do not. Both “B” and “C” give a yellow precipitate when heated with iodine in the presence of NaOH. Compound “D” gives brisk effervescence with sodium bicarbonate solution. Identify “A”, “B”, “C” and “D” given the number of carbon atoms in three of these carbon compounds is three while one has two carbon atoms. Give an explanation for our answer.
Advertisements
उत्तर
A, B and C contain carbonyl group as they give positive 2, 4 DNP test
A and B are aldehydes as aldehydes reduce Tollen’s reagent
C is a ketone, as it contains carbonyl group but does not give positive Tollen’s test
C is a methyl ketone as it gives positive iodoform test
B is an aldehyde that gives positive iodoform test
D is a carboxylic acid
Since the number of carbons in the compounds A, B, C and D is three or two
B is CH3CHO as this is only aldehyde which gives a positive iodoform test
The remaining compounds A, C and D have three carbons
A is \[\ce{CH3CH2CHO}\], C is \[\ce{CH3COCH3}\] and D is \[\ce{CH3CH2COOH}\]
APPEARS IN
संबंधित प्रश्न
Out of CH3CH2 – CO – CH2 – CH3 and CH3CH2 – CH2 – CO – CH3, which gives iodoform test?
Give a simple chemical test to distinguish between the following pair of compounds:
Phenol and Benzoic acid
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.
Complete the synthesis by giving missing starting material, reagent or product.

Fehilng's test is positive for
An organic compound neither reacts with neutral ferric chloride solution nor with Fehling solution. It however, reacts with Grignard reagent and gives positive iodoform test. The compound is:
Choose the reaction which is not possible:
An organic compound 'A' with molecular formula C5H8O2 is reduced to n-pentane with hydrazine followed by heating with NaOH and glycol. 'A' forms a dioxime with hydroxylamine and gives a positive iodoform and Tollen's test. Identify 'A' and give its reaction for iodoform and Tollen's test.
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 ______.





