Identify the mechanism (E1 or E2) the reaction is undergoing and draw a stepwise mechanism for the following reaction that shows how all four products were formed. Show all intermediates and indicate electron movement with arrows. The image represents a chemical reaction involving an organic compound. The initial reactant is a chlorocyclohexene derivative, specifically a 1-chloro-1-methylcyclohexene. When this compound reacts with methanol (CH₃OH), several products are formed:1. The first product is a methoxycyclohexene, where the chlorine atom has been replaced by a methoxy group (-OCH₃) on the cyclohexene ring.2. The second product is a toluene compound, with a methyl group attached to the benzene ring.3. The third product is a methoxytoluene, with the methoxy group replacing the chlorine atom and a methyl group also present on the benzene ring.4. The fourth product is a methylbenzene or toluene.5. Additionally, hydrochloric acid (HCl) is produced as a byproduct.This reaction sequence demonstrates nucleophilic substitution and elimination processes, important concepts in organic chemistry.

Alkyl halide when undergoes reaction with CH3OH forms alkene with an elimination reaction mechanism.Tertiary alkyl halide undergoes with bimolecular elimination reaction mechanism, E-2. Alkyl halide when reacts with methanol, then Nucleophilic substitution reaction also occurs which replaces the Cl- nucleophile with OCH3.The reaction mechanism is –