These two alkyl halides are diastereomers of one another. draws the byproducts of each elimination as antiperiplanar stereochemistry is carried out.
Bimolecular elimination is referred to as an E2 mechanism, which is essentially a one-step mechanism. Here, a new double bond is formed mostly as a result of the carbon-hydrogen and carbon-halogen bonds breaking. The rate-determining step of the E2 mechanism, however, includes a base, which has a significant impact on the process.
The pace of the reaction increases together with the substrate concentration. E2: The term "2" refers to the fact that this is a second-order bimolecular reaction. Accordingly, the rate of reaction is influenced by both the substrate.
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