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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.
- Identify (A), (B) and (C).
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- Write the equation for iodoform test for C.
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Which among the above compound/s does/do not form Silver mirror when treated with Tollen's reagent?
The major products formed in the following reaction sequence A and B are:
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)
The reagent that can be used to distinguish acetophenone and benzophenone is ______.
