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sulphuric acid and sodium dichromate are standard oxidation agents for alcohols. Primary and secondary alcohols behave differently. mixed with ethanol warmed lightly and gently distilled they produce ethanal (an Aldehyde), but put through a reflux distillation they will eventually produce ethanoic acid (vinegar). The only way you can know which you have is by testing with an indicating agent like Fehlings solution, or the smell!!

So the process is as important as the chemicals involved!

However, 2-hexanol is a secondary alcohol, with the OH on the second carbon so 2-hexanol oxidises into 2-hexanone, which is a ketone and therefore can not be oxidised any further.

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10y ago
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11y ago

Explanation:

When cyclohexene reacts with concentrated sulfuric acid, the higher electron density pi-bond, the double bond of cyclohexene, attacks one of the easily donated hydrogens of sulfuric acid and protonates one of the sp2 hybridized carbons. This results that the other carbon that had a double bond becomes a carbocation with an empty p-orbital. The anion that was left from the sulfuric acid after the first step now attacks the carbocation linking the sulfuric anion to the carbon ring.

Conclusion:

The product is Cyclohexyl hydrogen sulfate.

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11y ago

In this reaction you are hydrating an alkene. The double bond is broken and the product is cyclohexanol.

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11y ago

Cyclohexyl sulfate. Draw a hexagon. At five corners of the hexagon, write -CH2-. At the sixth corner write >CH-O-SO3H.

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12y ago

it's an octane ring with an OH group attached

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13y ago

1-methylcyclohexene, water, sulfuric acid

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13y ago

cyclohexanol

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9y ago

because people dont like doing jobs

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Q: What is the product of 1-methylcyclohexanol sulfuric acid?
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