Which alcoholic group is most reactive for dehydration by concentrated h2so4?

Which alcohol is most reactive for dehydration?

Since the carbocation is most stable in the case of tertiary alcohols, the rate of dehydration is highest for tertiary alcohols in comparison to secondary and primary alcohols.

What does concentrated H2SO4 do to an alcohol?

Concentrated sulfuric acid produces messy results. Because sulfuric acid is also a strong oxidizing agent, it oxidizes some of the alcohol to carbon dioxide and is simultaneously reduced itself to sulfur dioxide. Both of these gases must be removed from the alkene.

Which of the following alcohols gives 2 Butenc on dehydration by conc H2SO4?

Answer. 2-butene can be obtained by dehydration of Butane-2-ol by using concentrated H SO . Hence , the option (c) is the correct answer .

Which alcohol is most reactive towards dehydration of alcohol in acid catalysed reaction?

So, option A is the most reactive towards the acid-catalysed dehydration.

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Can primary alcohols be dehydrated?

Primary alcohols dehydrate through the E2 mechanism. … Secondary and tertiary alcohols dehydrate through the E1 mechanism. Similarly to the reaction above, secondary and tertiary –OH protonate to form alkyloxonium ions. However, in this case the ion leaves first and forms a carbocation as the reaction intermediate.

Which is more reactive towards hydration?

More-stable alkene is less reactive and less-stable alkene is more reactive.

Why is concentrated H2SO4 used in dehydration?

Hydrated crystals can be dehydrated with concentrated H2SO4. This is because it readily absorbs water from the crystal/ molecule/ compound. So, it is used as dehydrating agent. It is used as a dehydrating agent mainly in contact process.

Which alcohol can be oxidised by acidified potassium dichromate VI but Cannot be dehydrated?

(h) Draw the structure of the isomer of A that cannot be dehydrated to form an alkene by reaction with concentrated sulfuric acid. Ethanol can be oxidised by acidified potassium dichromate(VI) to ethanoic acid in a two-step process.

Is dehydration of alcohol reversible?

This process is usually reversible. In the second step, the protonated alcohol loses water to give a positively charged species known as a carbonium ion or carbocation. Finally the carbonium ion loses a proton to give alkene.

Which of the following alcohols will give the most stable carbocation during dehydration?

The tertiary carbocation formed during dehydration of 2-methyl-2-propanol is most stable.

What is dehydration of alcohol?

When alcohol reacts with protic acids it tends to lose a molecule of water in order to form alkenes. These reactions are generally known as dehydration of alcohols. It is a basic example of an elimination reaction.

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Which alcohol will not undergo dehydration to produce an alkene?

If the reaction is not sufficiently heated, the alcohols do not dehydrate to form alkenes, but react with one another to form ethers (e.g., the Williamson Ether Synthesis). Alcohols are amphoteric; they can act both as acid or base. The lone pair of electrons on oxygen atom makes the –OH group weakly basic.

What are symptoms of dehydration?


  • feeling thirsty.
  • dark yellow and strong-smelling pee.
  • feeling dizzy or lightheaded.
  • feeling tired.
  • a dry mouth, lips and eyes.
  • peeing little, and fewer than 4 times a day.
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