Compound A, an alkyl bromide with chemical formula , reacts with to yield compound B. Compound B in turn reacts with (1) , (2) ,

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Compound A, an alkyl bromide with chemical formula , reacts with to yield compound B. Compound B in turn reacts with (1) , (2) ,

to yield compound C. Compound C reacts with to yield compound D. Propose a structure for compound D that is consistent with the following predicted 1H-NMR spectrum.

Chemistry

1 answer:

leonid [27] · Answer 1 · 2023-07-14T03:53:02+03:00

Compound B will be propene as a result of an elimination reaction involving potassium tert-butoxide and an alkyl halide. In proton NMR, alkenes exhibit signals in the 5–6 ppm range.

<h3>What are Elimination Reactions?</h3>

Elimination reactions are one sort of reaction that are mostly utilized to convert saturated compounds (organic molecules that contain single carbon-carbon bonds) to unsaturated compounds (compounds that feature double or triple carbon-carbon bonds). Additionally, it plays a significant role in the production of alkenes.

The elimination response is composed of the following three major events:

Proton exclusion.
The synthesis of a C-C pi bond.
As a result, the relationship between the departing group's members has grown increasingly distant.

To learn more about Elimination reactions visit:

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