Alcohols, Phenols and Ethers
Dehydration of alcohols can be done by using:
Which is the best reagent to convert cyclohexanol into cyclohexene?
Cyclohexanol is used as substrate and phosphoric acid is present as catalyst which promotes the reaction but is not consumed in it. The hydroxyl group in R-OH is a poor leaving group because it leaves as hydroxide ion. An acid is used to protonate the alcohol and form $${ R-OH }_{ 2 }^{ + }$$
Dehydration of alcohols can be done by using:
State how the following conversions can be carried out. Ethyl alcohol to Ethene.
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:
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.
In the following dehydration of diol with $$\displaystyle { H }_{ 3 }{ PO }_{ 4 }$$, following product is: