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प्रश्न
Write chemical reactions of following reagents on methoxyethane:
dilute H2SO4
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उत्तर
\[\ce{\underset{Methoxyethane}{CH3 - O - C2H5} + H2O ->[Δ][H2SO4] \underset{Methanol}{CH3OH} + \underset{Ethanol}{C2H5OH}}\]
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संबंधित प्रश्न
Write the mechanism of the following reaction :
\[\ce{C2H5OH->[H2SO4][443K]CH2=CH2 + H2O}\]
Methanol and ethanol are miscible in water due to ____________.
If ethanol dissolves in water, then which of the following would be observed:
Wood spirit is known as acetone:
Phenol can be distinguished from ethanol by the reactions with:
(i) \[\ce{Br2/water}\]
(ii) \[\ce{Na}\]
(iii) Neutral \[\ce{FeCl3}\]
(iv) All the above
Write the IUPAC name of the following compound.
\[\begin{array}{cc}
\phantom{.}\ce{CH3 - CH - CH - CH - CH - CH3}\phantom{}\\
\phantom{......}|\phantom{......}|\phantom{......}|\phantom{.....}|\phantom{........}\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{C2H5}\phantom{.}\ce{OH}\phantom{...}\end{array}\]
What is denatured alcohol?
Suggest a reagent for conversion of ethanol to ethanal.
Suggest a reagent for conversion of ethanol to ethanoic acid.
Dipole moment of phenol is smaller than that of methanol. Why?
The carbon-oxygen bond in phenol is slightly stronger than that in methanol. Why?
Arrange water, ethanol and phenol in increasing order of acidity and give reason for your answer.
Assertion: Ethanol is a weaker acid than phenol.
Reason: Sodium ethoxide may be prepared by the reaction of ethanol with aqueous \[\ce{NaOH}\].
Convert the following:
Propanenitrile to ethanol.
Tonics in general contain
Liquor poisoning is due to
Alcoholic fermentation is brought about by the action of
If the starting material is 1-methyl-1,2-epoxy cyclopentane, of absolute configuration, decide which one compound correctly represents the product of its reaction with sodium methoxide in methanol.
Convert the following Ethanal to ethanol.
How methanol is obtained from methanal.
Give IUPAC names of the following compounds:
\[\begin{array}{cc}
\ce{CH3 - CH - CH - CH - CH2-OH }\\
|\phantom{......}|\phantom{......}|\phantom{.......}\\
\ce{Cl}\phantom{....}\ce{CH3}\phantom{...}\ce{CH3}\phantom{.....}
\end{array}\]
3, 3-dimethyl-1-butene was subject to following reactions:
