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प्रश्न
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
|\phantom{....................}|\phantom{.........}|\phantom{.............}\\
\ce{OH}\phantom{................}\ce{OH}\phantom{...}\ce{C{_2}H5}\phantom{.........}\\
\end{array}\]
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उत्तर
5-Ethylheptane-2,4-diol
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संबंधित प्रश्न
Write the IUPAC name of the given compound:
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{........................}\ce{CH3}\\
\phantom{....................}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.........}|\phantom{.........}|\\
\phantom{...}\ce{CH3}\phantom{....}\ce{OH}\phantom{....}\ce{CH3}\\
\end{array}\]
Give the IUPAC name of the following ether:
O2N – C6H4 – OCH3(p)
Give the IUPAC name of the following ether:
CH3CH2CH2OCH3
Write IUPAC name of the following compound (CH3)2 N − CH2CH3
Resorcinol on distillation with zinc dust gives _________.
Write structural formulae for 1-Ethylcyclohexanol.
Write IUPAC names of the following
C6H5OCH2CH3 is called:
One of the following is not a dihydroxy derivative of benzene.
Ethylene reacts with Baeyer’s reagent to give ______.
\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]
\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]
The product ‘Z’ is:
Write the IUPAC name of the compound given below.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH2 - C = C - OH}\\
\phantom{........}|\phantom{....}|\phantom{}\\
\phantom{..............}\ce{CH3 CH2OH}
\end{array}\]
Arrange the following compounds in decreasing order of acidity.
\[\ce{H2O, ROH, HC ≡ CH}\]
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.
Write the IUPAC name of the following compound.
Convert the following:
Ethyl alcohol into ethyl acetate.
How are the following conversions carried out?
Methyl magnesium bromide→2-Methylpropan-2-ol.
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
