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An organic compound of molecular formula \[{C_4}{H_6}\] (A), forms precipitate with ammoniacal silver nitrate and ammoniacal cuprous chloride. ‘A’ has an isomer ‘B’, one mole of which reacts with one mole of \[B{r_2}\] to form 1,4-dibromo-2-butene. Another isomer of ‘A’ is ‘C’, 1 mole of C reacts with only 1 mole of \[B{r_2}\]to give vicinal dibromide. A, B & C.
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Last updated date: 22nd Sep 2024
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Hint: First thing we have to do in this reaction is to find the compound A from the molecular formula given. Then only we will be able to carry out the further reaction and then find the compound B and C.

Complete answer:
An organic compound is given which has a molecular formula of \[{C_4}{H_6}\]. When the compound A reacts with the ammoniacal silver nitrate and ammoniacal cuprous chloride, it will form a precipitate. Hence, the compound A was found to be 1-Butyne.
1-Butyne is having an isomer, i.e., the compound B. One mole of the compound B will react with one mole of the bromine molecule to form 1,4-Dibromo-2-butene. Therefore, the compound B was found to be 1,4-Butadiene.
Butyne is also having another isomer other than 1,4-Butadiene, i.e., the compound C. One mole of the compound C will react with one mole of the Bromine molecule to give vicinal dibromide. Therefore, the compound C is found to be 1-Cyclobutene.

Therefore, the correct answer is option (A).

Note:
We should always be careful while finding the compound A, because by knowing it only we would be able to carry out the rest of the reaction. If we make a mistake in finding it, then there is a chance that the whole reaction can go wrong.