Question

Part A Predict the product formed when the structure shown below undergoes reaction with conc. HBr. Interactive 3D display mode H,C OH Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.

Answer 1

Answers не ле Explanation: The structure provided is an primary alcohol called propanol, which undergoes SN2 reaction with concentrated Hydrobromic acid (conc. HBr) to give i-Bromobutane as a product. primary alcohols cannot undergo sul reaction because primary carbocations are too unstable to be formed. for the SN² reaction of mechanism an alcohol step-1: the given acid (conc. HBY) protonates the most basic atom in the reactant conygen atom) to make it a better leaving group, be displaced by a nucleophile Hem OHFHBr - He noter Step-2: ile (Br) attacks the back side of the carbon The Nucheophile (Br) attacks the back and displaces the leaving group in a single step - Bod slow step [Br... on Henry RDS ... C OHA THEM Br BY SN Transition State