the reaction in this experiment is the reverse of the hydration of cyclohexene to form cyclohexanol. both reactions are acid catalyzed. how does the use of the hickman still favor the desired product? (review carey 6.9.)

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14-11-2022
Chemistry

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the reaction in this experiment is the reverse of the hydration of cyclohexene to form cyclohexanol. both reactions are acid catalyzed. how does the use of the hickman still favor the desired product? (review carey 6.9.)

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kjuli1766 kjuli1766 · Answer 1 · 2022-11-20T06:43:17+01:00

The reaction in this experiment is the reverse of the hydration of cyclohexene to form cyclohexanol is OH H⁺ + H₂O

The forward and backsword reactions are plausible in acidic conditions. To avoid this a special debilitation apparatus is used ic. Chicken al distillation apparatus. The precious, expeckenbeserve besi bugs point 86 degrees C is much lower than the cyclohexanol 165 degrees C. So if the distillation happens, the product evaporates no son as it comes in the reaction and is collected in a separate vessel.

So it would be in contact with acid or reaction mixture for much time. The distillate will contain only the product whereas bestizoru lacy in the reduction veal in eye labels real would Oneida. The feedstock is contaminated with water, unreacted alcohol, phosphoric acid, and some byproducts. Washing with water removes most contaminants. Treatment with sodium carbonate solution removes traces of acid and a final water wash removes the remaining carbonates. Synthesis of alkenes dehydration of cyclohexanol.

Learn more about The hydration of cyclohexene here:-https://brainly.com/question/22278424

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