A hydrocarbon $\left(\mathrm{A}\right)$ with molecular formula ${\mathrm{C}}_5{\mathrm{H}}_{10}$ on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of $\mathrm{NaOH}$ while only (B) give a silver mirror on reaction with Tollen’s reagent. Identify (A), (B) and (C).

A hydrocarbon $\left(\mathrm{A}\right)$ with molecular formula ${\mathrm{C}}_5{\mathrm{H}}_{10}$ on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of $\mathrm{NaOH}$ while only (B) give a silver mirror on reaction with Tollen’s reagent. Write the reaction of B with Tollen’s reagent.

A hydrocarbon $\left(\mathrm{A}\right)$ with molecular formula ${\mathrm{C}}_5{\mathrm{H}}_{10}$ on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of $\mathrm{NaOH}$ while only (B) give a silver mirror on reaction with Tollen’s reagent. Write the equation for iodoform test for C.

A hydrocarbon $\left(\mathrm{A}\right)$ with molecular formula ${\mathrm{C}}_5{\mathrm{H}}_{10}$ on ozonolysis gives two products (B) and (C). Both (B) and (C) give a yellow precipitate when heated with iodine in presence of $\mathrm{NaOH}$ while only (B) give a silver mirror on reaction with Tollen’s reagent. Write down the equation for aldol condensation reaction of B and C.