Dehydration Of Cyclohexanol

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Discussion & Conclusion In this experiment we learned how to synthesize the cyclohexene by dehydration of cyclohexanol. We procedure the first step where we have to mix the components. Then we heat the R.B.F with a fractionating column, distilled water. Then we obtained the layers, and we transferred the organic layer to a small, dry Erlenmeyer flask. We added anhydrous Sodium Sulfate as a drying agent. To complete, we distilled the cyclohexene and collected the product. Knowing this data, we determined the yield % which is 58.5%. This experiment features the dehydration of cyclohexanol and produce cyclohexene. The acid catalyzed dehydration of cyclohexanol with distillative removal of the resulting cyclohexene from the reaction mixture…show more content…
This technique prevents the product to contact other reactants, and leave the heating environment which might cause side reactions. The removal of the product also helps to shift the equilibrium position of the incomplete reaction to the right hand side, and prevents backwards reaction, resulting in an increased yield of products. This experiment also introduces the idea of azeotrope. An azeotrope is a mixture of two or more pure compounds in such a ratio that its composition cannot be changed by simple distillation. This is because when an azeotrope is boiled, the resulting vapour has the same ratio of constituents as the original mixture of liquids. Each azeotrope has a characteristic boiling point. The boiling point of an azeotrope is either less than the boiling points of any of its constituents (a positive azeotrope), or greater than the boiling point of any of its constituents (a negative azeotrope). The azeotropes of cyclohexanol/water and cyclohexene/water are both positive azeotropes. The separation of cyclohexene could not depend on distillation alone. The method used in our experiment is one way that we could employ to separate azeotropes into its constituents. By adding a chemical that could form complex with one of the component, in our case, CaCl2 forms complex with water,…show more content…
The only thing that's somewhat similar are the -CH2- peaks between 1ppm and 2ppm, although there are five CH2 groups in cyclohexanol in three chemically equivalent groups, and only 4 CH2 groups in cyclohexene in two equivalent groups, so they look very different in the spectrum.The rest of it is not even similar at all: in cyclohexene, the equivalent sp2-hydrogens give a signal at 5.6ppm, and that's it in cyclohexanol, the -CH- hydrogen connected to the oxygen has a qiuntuplet (in first order approximation) about 3.5ppm, and the -OH hydrogen itself has a signal which is pH-dependent, can be anywhere from 2 to
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