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Convert Cyclohexanol to Cyclohexene via a Acid-Catalyzed Dehydration reaction 1. Why does the product ‘come over’...

Convert Cyclohexanol to Cyclohexene via a Acid-Catalyzed Dehydration reaction

1. Why does the product ‘come over’ after being formed? Please think about the properties of the starting material and product.
2. If there was no acid present, would you expect to get a product? Why/why not?
3. If we start off with 10 molecules of the starting alcohol and only get an 80% yield, how many molecules will we find in the product flask?
4. Look up the concept of 'moles' and then answer question 3 again, but this time consider if we started with 10 grams of cyclohexanol. Consult your instructor if you have problems understanding the concept of moles.

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