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प्रश्न
Write the IUPAC name of the following compound:
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उत्तर
2,6-Dimethylphenol
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संबंधित प्रश्न
Name the following compound according to the IUPAC system.
\[\begin{array}{cc}
\ce{H2C = CH - CH - CH2 - CH2 - CH3}\\
|\phantom{...............}\\
\ce{OH}\phantom{............}
\end{array}\]
Write the IUPAC name of the following compound:
C6H5 – O – C7H15(n−)
Give the IUPAC name of the following ether:
\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.........}|\\
\phantom{.............}\ce{CH3}
\end{array}\]
Give the IUPAC name of the following ether:
Write the structures of the products when Butan-2-ol reacts with CrO3
Propanoic acid to ethylamine.
C6H5OCH2CH3 is called:
The compound HOCH2 – CH2OH is __________.
Cresol has ____________.
HBr reacts fastest with ____________.
IUPAC name of m-cresol is ____________.
1-Propanol and 2-propanol can be best distinguished by:
Which of the following reagents can be used to oxidise primary alcohols to aldehydes?
(i) \[\ce{CrO3}\] in anhydrous medium.
(ii) \[\ce{KMnO4}\] in acidic medium.
(iii) Pyridinium chlorochromate.
(iv) Heat in the presence of Cu at 573 K.
Write the IUPAC name of the compound given below.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH2 - C = C - OH}\\
\phantom{........}|\phantom{....}|\phantom{}\\
\phantom{..............}\ce{CH3 CH2OH}
\end{array}\]
Assertion: Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.
Reason: Lewis acid polarises the bromine molecule.
How are the following conversions carried out?
Methyl magnesium bromide→2-Methylpropan-2-ol.
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{..............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.....}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{.}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
