A hydrocarbon, compound A (C6H10), burned with a yellow, almost nonsmoky flame. On catalytic hydrogenation over platinum catalyst, it absorbed 1 mol of hydrogen to form compound B. It also decolorized a Br2–CH2Cl2 solution to yield a dibromo derivative, compound C. Ozonolysis of the hydrocarbon gave only one compound, D. Compound D gave a positive iodoform test when treated with iodine–sodium hydroxide solution. On treatment of compound D with an alcoholic solution of silver ammonium hydroxide, a silver mirror was formed within a few minutes. Identify the hydrocarbon A and compounds B–D.Identify the hydrocarbon A and compounds B–D.
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