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प्रश्न
Give the equation of the following reaction:
Oxidation of propan-1-ol with alkaline KMnO4 solution.
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उत्तर
\[\ce{\underset{propan-1-ol}{CH3CH2CH2OH} + 2[O] ->[Alkaline KMnO4][Oxidation] \underset{Propanoic acid}{CH3CH2COOH} + H2O}\]
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संबंधित प्रश्न
Write the final product(s) in each of the following reactions:
Give reasons for the following:
o-nitrophenol is more acidic than o-methoxyphenol.
Name the reagent used in the following reaction:
Oxidation of a primary alcohol to aldehyde.
The compound which reacts fastest with Lucas reagent at room temperature is:
By which of the following methods alcohol can be prepared in excellent yield?
Which of the following are used to convert RCHO into RCH2OH?
(i) H2/Pd
(ii) LiAlH4
(iii) NaBH4
(iv) Reaction with RMgX followed by hydrolysis
The compound which gives the most stable carbonium ion on dehydration is:
Mark the correct increasing order of reactivity of the following compounds with HBr/HCl.
| (a) |  |
| (b) |  |
| (c) |  |
Name the factors responsible for the solubility of alcohols in water.
Explain why is OH group in phenols more strongly held as compared to OH group in alcohols.
Ethers can be prepared by Williamson synthesis in which an alkyl halide is reacted with sodium alkoxide. Di-tert-butyl ether can’t be prepared by this method. Explain.
Which of the following observation is shown by 2-phenyl ethanol with Lucas Reagent?
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.
Write the mechanism of acid dehydration of ethanol to yield ethene.
