Advertisements
Advertisements
Question
Give the equation of the following reaction:
Oxidation of propan-1-ol with alkaline KMnO4 solution.
Advertisements
Solution
\[\ce{\underset{propan-1-ol}{CH3CH2CH2OH} + 2[O] ->[Alkaline KMnO4][Oxidation] \underset{Propanoic acid}{CH3CH2COOH} + H2O}\]
APPEARS IN
RELATED QUESTIONS
Write the mechanism of the following reaction :

Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.
Show how will you synthesize pentan-1-ol using a suitable alkyl halide.
Give the equation of the following reaction:
Treating phenol with chloroform in the presence of aqueous NaOH.
When 3-methylbutan-2-ol is treated with HBr, the following reaction takes place:
\[\begin{array}{cc}
\phantom{...................................}\ce{Br}\\
\phantom{..................................}|\\
\ce{CH3 - CH - CH - CH3 ->[HBr] CH3 - C - CH2 - CH3}\\
|\phantom{.........}|\phantom{...................................}|\phantom{...........}\\
\ce{CH3}\phantom{...}\ce{OH}\phantom{...............................}\ce{CH3}\phantom{.......}\\
\end{array}\]
Give a mechanism for this reaction.
(Hint: The secondary carbocation formed in step II rearranges to a more
stable tertiary carbocation by a hydride ion shift from 3rd carbon atom.)
Lucas reagent is ____________.
By which of the following methods alcohol can be prepared in excellent yield?
Primary and secondary alcohols on the action of reduced copper give:
The compound which gives the most stable carbonium ion on dehydration is:
Cyclohexene is best prepared from cyclohexanol by which of the following:
During dehydration of alcohols to alkenes by heating with cone. H2SO4 the initial step is ____________.
Explain why nucleophilic substitution reactions are not very common in phenols.
Assertion: Bond angle in ethers is slightly less than the tetrahedral angle.
Reason: There is a repulsion between the two bulky (–R) groups.
Which of the following alcohols will not undergo oxidation?
Write the mechanism of acid dehydration of ethanol to yield ethene.
Write the mechanism of acid dehydration of ethanol to yield ethene.
Write the mechanism of acid dehydration of ethanol to yield ethene.
Write the mechanism of acid dehydration of ethanol to yield ethene.
