Advertisements
Advertisements
प्रश्न
Phenol is less acidic than ______.
पर्याय
ethanol
o-nitrophenol
o-methylphenol
o-methoxyphenol
Advertisements
उत्तर
Phenol is less acidic than o-nitrophenol.
Explanation:
In o-nitrophenol, nitro group is present at ortho position. Presence of electron-withdrawing group at ortho position increases the acidic strength. On the other hand, in o-methylphenol and in o-methoxyphenol and in o-methoxyphenol, electron releasing group \[\ce{(-CH3-OCH3)}\]
Presence of these groups at ortho or para positions of phenol decreases the acidic strength of phenols. So, phenol is less acidic than o-nitrophenol.
APPEARS IN
संबंधित प्रश्न
How do you convert the following:
Ethanol to Propan-2-ol
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:
Write the IUPAC name of the following compound.
\[\begin{array}{cc}
\phantom{.}\ce{CH3 - CH - CH - CH - CH - CH3}\phantom{}\\
\phantom{......}|\phantom{......}|\phantom{......}|\phantom{.....}|\phantom{........}\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{C2H5}\phantom{.}\ce{OH}\phantom{...}\end{array}\]
Suggest a reagent for conversion of ethanol to ethanoic acid.
Arrange the following compounds in increasing order of acidity and give a suitable explanation.
Phenol, o-nitrophenol, o-cresol
Name the enzymes and write the reactions involved in the preparation of ethanol from sucrose by fermentation.
Dipole moment of phenol is smaller than that of methanol. Why?
Arrange water, ethanol and phenol in increasing order of acidity and give reason for your answer.
Convert the following:
Propanenitrile to ethanol.
Tonics in general contain
Liquor poisoning is due to
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:
