Question

Question: Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] ${\mathit{H}}_{\mathbf{2}}\mathit{O}\mathbf{,}\mathbf{}{\mathit{H}}_{\mathbf{2}}\mathit{S}{\mathit{O}}_{\mathbf{4}}$; or [2] $\mathit{B}{\mathit{H}}_{\mathbf{3}}$followed by ${\mathit{H}}_{\mathbf{2}}{\mathit{O}}_{\mathbf{2}}\mathbf{,}\mathbf{}\mathit{H}{\mathit{O}}^{\mathbf{-}}$.

Short answer

Answer

Step-by-step solution

Step 1:Addition reaction of an alkene

Hydroboration-oxidation reaction involves the formation of a primary alcohol, whereas acid-catalyzed hydration reaction involves the formation of a secondary alcohol.

Formation of products for a, b and c