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प्रश्न
Name the following compound according to IUPAC system.
\[\begin{array}{cc}
\phantom{............}\ce{CH2OH}\\
\phantom{......}|\\
\ce{CH3 - CH2 - CH - CH - CH - CH3}\\
\phantom{......}|\phantom{............}|\phantom{.}\\
\phantom{........}\ce{CH2Cl}\phantom{......}\ce{CH3}\phantom{}
\end{array}\]
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उत्तर
3-Chloromethyl-2-isopropylpentan-1-ol
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संबंधित प्रश्न
Name the following compound according to IUPAC system.

Name the following compound according to IUPAC system.
\[\begin{array}{cc}
\ce{CH3 - C = C - CH2OH}\\
\phantom{}|\phantom{....}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{.}\ce{Br}\phantom{...}
\end{array}\]
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3\phantom{.}}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
Give IUPAC name of the following ether:
O2N – C6H4 – OCH3(p)
What is the action of hot HI on it?
Write structural formula for pentane-1,4-diol.
Write structural formulae for Cyclohex-2-en-1-ol.
Write IUPAC name of the following

Write IUPAC names of the following

Ethyl alcohol is industrially prepared from ethylene by:
The heating of phenyl methyl ether with HI produces:
IUPAC name of m-cresol is ______.
Explain why p-nitrophenol is more acidic than phenol.
Assertion: Phenols give o- and p-nitrophenol on nitration with conc. \[\ce{HNO3}\] and \[\ce{H2SO4}\] mixture.
Reason: –OH group in phenol is o–, p– directing.
Explain why Lewis acid is not required in bromination of phenol?
Identify A and B in the following:

Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
Draw structure of the following compound.
2-Methoxypropane
Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
