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प्रश्न
Write the IUPAC name of the following compound:
C6H5 – O – C2H5
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उत्तर
Ethoxybenzene
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संबंधित प्रश्न
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
|\phantom{....................}|\phantom{.........}|\phantom{.............}\\
\ce{OH}\phantom{................}\ce{OH}\phantom{...}\ce{C{_2}H5}\phantom{.........}\\
\end{array}\]
Write the IUPAC name of the following compound:
Which of the following compounds is NOT prepared by the action of alcoholic NI3 on alkyl halide?
(a) CH3NH2
(b) CH3- CH2- NH2
(c) CH3 - CH2 - CH2 - NH2
(d) (CH3)3 C- NH2
Write the structure and IUPAC name of 'methyl-n-propyl ether'.
Write the IUPAC name of the following :
Write a structural formula for methyl vinyl ether.
Write structural formulae for 1-Ethylcyclohexanol.
Write IUPAC names of the following
One of the following is not a dihydroxy derivative of benzene.
The product of acid catalysed hydration of 2-phenylpropene is:
Among the following sets of reactants which one produces anisole?
Arrange the following compounds in decreasing order of acidity.
\[\ce{H2O, ROH, HC ≡ CH}\]
Write steps to carry out the conversion of phenol to aspirin.
Match the structures of the compounds given in Column I with the name of the compounds given in Column II.
| Column I | Column II | |
| (i) |  |
(a) Hydroquinone |
| (ii) |  |
(b) Phenetole |
| (iii) |  |
(c) Catechol |
| (iv) |  |
(d) o-Cresol |
| (v) |  |
(e) guinone |
| (vi) |  |
(f) Resorcinol |
| (g) Anisole |
Explain why Lewis acid is not required in bromination of phenol?
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 IUPAC names of the following compounds:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3\phantom{...}OH\phantom{...}CH3}\\
\end{array}\]
