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A hydrocarbon (A) with molecular formula C5H10 on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of NaOH while only (B) give a silver mirror on reaction with Tollen’s reagent.
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- Write down the equation for aldol condensation reaction of B and C.
Choose the reaction which is not possible:
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.
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:
