Alcohols, Phenols and Ethers
Dehydration of alcohols can be done by using:
In the following sequence of reactions, $$CH_3Br\overset{KCN}{\rightarrow}A\overset{H_3O^+}{\rightarrow}B\overset{LiAlH_4}{\rightarrow}C$$ The end product C is:
The end product C is ethyl alcohol.
$$\displaystyle CH_3Br \overset{KCN}{\rightarrow}\underset {A}{CH_3-CN}\overset{H_3O^+}
{\rightarrow}\underset {B}{CH_3-COOH}\overset{LiAlH_4}{\rightarrow}\underset {C}{CH_3-CH_2-OH}$$
Methyl bromide reacts with KCN to form acetonitrile. Br atom is replaced with CN group. Hydrolysis of cyano group gives carboxylic group. Reduction of carboxylic group gives hydroxyl group.
Dehydration of alcohols can be done by using:
State how the following conversions can be carried out. Ethyl alcohol to Ethene.
Which of the following alcohols will give the most stable carbocation during dehydration?
Explain mechanism of acid catalyses dehydration of ethyl alcohol?
The major product of the above reaction is :
Acid catalysed dehydration of t-butanol is faster than that of n-butanol because:
Choose the correct answer among the alternatives given: In the following reactions, (i)$$CH_3-\overset{CH_3}{\overset{|}C}H-\underset{OH}{\underset{|}C}H-CH_3\xrightarrow{H^+/heat}\underset{[Major\ product]}A +\underset{[Minor\ product]} B$$ (ii)$$A\xrightarrow[in\,absence\,of \,peroxide]{HBr,dark}\underset{Major\ product}C+\underset{Minor\ product}D$$ The major products $$A$$ and $$C$$ are respectively?
Name the reagents used in the following reaction: Dehydration of propan-2-ol to propene.
Which is the best reagent to convert cyclohexanol into cyclohexene?
In the following dehydration of diol with $$\displaystyle { H }_{ 3 }{ PO }_{ 4 }$$, following product is: