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The reaction causes the protonation of the alcohol group, which causes it to turn into a water, which is a good leaving group. As a result, the water leaves, creating a carbocation with a positive charge. The carbocation then loses the proton (positive charge) forming a mixture of alkenes.

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13y ago
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15y ago

1-methylcyclohexanol + phosphoric acid or 1 menthyl - cyclohex - 1 - ene. It should appear as the dominant product.

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Q: Outline a mechanism for the dehydration of 4-methylcyclohexanol catalyzed by phosphoric acid?
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