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For the following dehydrohalogenation (E2) reaction, draw the Zaitsev product(s) resulting from the elimination involving C2-C3

For the following dehydrohalogenation (E2) reaction, draw the Zaitsev product(s) resulting from the elimination involving C2-C3 (i.e., the carbon atoms depicted with stereobonds). Show the product stereochemistry clearly. If there is more than one organic prodcut, both products may be drawn in the same box. Ignore elimination involoving C2 or C3 and any carbon atom other than C3 or C2.

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Concepts and reason

Dehydrohalogenation is the elimination reaction in which alkene is formed as a product by the elimination of hydrogen halide. This elimination reaction undergoes in the presence of a strong base. In this reaction, both hydrogen and halogen cleaves in a single step.

Fundamentals

Zaitsev’s rule: This rule states that, in the elimination reaction, the product that is more substituted is represented as a stable product.

An example for the elimination reaction:

In the above reaction, the elimination of proton and halogen takes place in the single step.

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