You asked: Which of the following alcohol gives the most stable carbocation during dehydration?

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

Which of the following alcohol is given for dehydration?

From the given alcohol, IV is a tertiary alcohol and III is a secondary alcohol. Therefore, these alcohols exhibit the most ease of dehydration of the given substances, with IV more so than III.

Which among the following alcohols will be the most reactive for dehydration?

Tertiary alcohol > secondary alcohol > primary alcohol. Electron attracting group present in alcohols increase the reactivity for dehydration. Greater is the -I effect of the group present in alcohol, more will be its reactivity.

Which alcohol is most stable?

Tert-butanol loses an −OH group to give most stable carbonium ion. The positive charge on carbon atom is stabilized by +I inductive effect of 3 methyl groups.

Which of the following is most stable carbo cation by dehydration?

Step by step solution by experts to help you in doubt clearance & scoring excellent marks in exams. 3∘ alcohols Me-Me∣C⊕-Me is most stable carbocation.

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Which alcohol is more easily hydrated?

Tertiary forms of alcohol are easiest to dehydrate as the carbocations are more stable and thus easier to form compared to primary and secondary carbocations.

Which is most easily dehydrated?

Thus, compound (a), in acidic conditions, will most readily be dehydrated.

What is the order of esterification?

The relative order of esterification of alcohols is 1>2>3. Thus as the steric hinderance (or bulkiness) increases from primary to secondary to tertiary alcohol, the order of esterification decreases.

Which is more reactive towards hydration?

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

Which of the following is not characteristic of alcohols?

They are lighter than water.

Why is 3 alcohol more reactive?

The tertiary alcohol is more reactive than other alcohols because of the presence of the increased number of alkyl groups. These alkyl group increases the +I effect in the alcohol.

What makes a Carbocation stable?

Carbocations Are Stabilized By Neighboring Carbon-Carbon Multiple Bonds. Carbocations adjacent to another carbon-carbon double or triple bond have special stability because overlap between the empty p orbital of the carbocation with the p orbitals of the π bond allows for charge to be shared between multiple atoms.

Why is 3rd degree alcohol more stable?

Tertiary alcohols are more reactive because the increased number of alkyl groups increases +I effect. So, the charge density on carbon atom increases and hence around oxygen atom. … Hence, the cleavage of C−O bond becomes easier. So, a tertiary carbocation is formed which is more stable than secondary and primary.

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How do you compare the rate of dehydration?

1 Answer. The rate of dehydration is related to the ease of formation of the carbocation and the energy of the carbocation intermediate. The ease of formation of carbocation is tertiary>secondary>primary. That is the ease of abstraction of OH2+ COULD BE be R>Q/S>P.

Which of the following Carbanion is most stable?

By releasing electron density towards the negatively charged C atom of carbanion, they intensify its negative charge and destabilize the carbanion. Thus, the stability of carbanions decreases with the increase in the number of alkyl groups.As a result, methyl anion, CH3:- having no alkyl group is the most stable.

What is acidic dehydration of alcohol?

Alcohol upon reaction with protic acids tends to lose a molecule of water to form alkenes. These reactions are known as dehydrogenation or dehydration of alcohols. It is an example of an elimination reaction.

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