Which of the following alcohols will most easily undergo acid catalyzed dehydration?

Which Alcohol undergo acid catalyzed dehydration most easily?

Which one of the following alcohols undergoes dehydration most easily? The reactivity order for dehydration of alcohols is tertiary alcohol > secondary alcohol > primary alcohol. Therefore, the alcohol, CH3 |CH3CH2-C-CH2CH3 | OH is dehydrated most rapidly.

Which alcohol would undergo a dehydration reaction the fastest?

Hence, alcohol given in option C will have the fastest rate of dehydration. Thus, option C is the answer. Note: Dehydration reaction is an example of an elimination reaction.

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.

Which of the following undergoes rapid acid catalysed dehydration?

Hence, t−Butanol from tertiary carbocation which has 9−α hydrogen undergo fast acid – catalyzed dehydration.

What is acid catalyzed dehydration?

Summary. When heated with strong acids catalysts (most commonly H2SO4, H3PO4), alcohols typically undergo a 1,2-elimination reactions to generate an alkene and water. Also known as dehydration since it involves the removal of a molecule of water.

INFORMATIVE:  Quick Answer: Do alcoholics binge eat?

Which of the following alcohols dehydrates most readily?

The alcohol that is dehydrated most easily with conc. H2SO4 is p−CH3OC6H4CH(OH)CH3.

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.

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.

Why is sulfuric acid used in dehydration of alcohols?

The acid catalysts normally used in alcohol dehydration are either concentrated sulfuric acid or concentrated phosphoric(V) acid, H3PO4. … 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.

Which is more reactive towards hydration?

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

What is the order of dehydration of primary secondary and tertiary alcohols?

The order of the ease of dehydration of alcohols is: tertiary > secondary > primary. Secondary and tertiary alcohols are best dehydrated by dilute sulfuric acid.

Which of the following would undergo dehydration?

Explanation: Dehydration reactions of alcohols leads to the formation of carbocations as is more stable than secondary and primary, thus, tertiary alcohol would undergo dehyderation fast.

INFORMATIVE:  Question: Can you drink alcohol the day after you finish antibiotics?

Which of the following undergoes dehydration?

Being tertiary in nature, alcohol undergoes dehydration most easily.

Which of the following is involved in acid catalysed dehydration of alcohols?

Solution : Acid catalysed dehydration of alcohol proceeds through a carbocation.

 All about addiction