Draw the arrow pushing mechanism for the following reaction The image depicts a chemical reaction involving an alkene and hydrochloric acid (HCl). The left side shows a molecular structure with an alkene functional group, represented by a double bond. This alkene reacts with HCl, which adds across the double bond in a typical electrophilic addition reaction.The reaction proceeds as follows:1. The double bond in the alkene reacts with HCl.2. The hydrogen atom (H) from HCl bonds to one of the carbon atoms in the double bond, breaking the double bond.3. The chloride ion (Cl-) then bonds to the other carbon atom.The result is a new molecular structure on the right side, where the original double bond has been converted into a single bond with a chlorine atom bonded to one of the carbons, indicating the formation of a chloroalkane.This example illustrates the mechanism of an electrophilic addition reaction, common in organic chemistry, where alkenes react with halogen acids to form haloalkanes.

Alkene reacts with hydrogen chloride to form alkyl chloride. The reaction proceeds via the electrophilic addition reaction mechanism. In the electrophilic addition reaction mechanism, a carbocation intermediate is formed and the carbonation is rearranged to a more stable carbocation.The mechanism of the reaction is as follows: Formation of carbonation: Carbocation is formed by the addition of electrophile (hydrogen cation). This step is a slow and rate-determining step of the reaction.Rearrangement in carbocation: The above formed secondary carbonation is rearranged to more stable tertiary carbonation by the transfer of hydrogen atom with the bonding electron pair.Addition of nucleophile: The chloride ion adds to the above formed tertiary carbonation to form the final product of the reaction.