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प्रश्न
- Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names.
- Classify the isomers of alcohols in the above question as primary, secondary and tertiary alcohols.
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उत्तर
- The isomeric alcohols with molecular formula C5H12O are:
- \[\ce{\underset{Pentanol (1^\circ)}{CH3 - CH2 - CH2 - CH2 - CH2 - OH}}\]
\[\begin{array}{cc}
\ce{CH3 - CH2 - CH2 - \overset{∗}{C}H - CH3}\\
\phantom{....................}|\\
\phantom{........................}\ce{\underset{Pentan-2-ol (2^\circ)}{OH}}\
\end{array}\]
\[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH2 - CH3}\\
|\phantom{..}\\
\phantom{..}\ce{\underset{Pentan-3-ol (2^\circ)}{OH}}\
\end{array}\]
\[\begin{array}{cc}
\ce{H3C - H2C - H\overset{∗}{C} - CH2OH}\\
\phantom{.........}|\\
\phantom{.............}\ce{\underset{2-Methylbutan-1-ol (1^\circ)}{CH3}}\
\end{array}\]
\[\begin{array}{cc}
\ce{CH3}\phantom{....................}\\
|\phantom{........................}\\
\ce{\underset{3-Methylbutan-1-ol (1^\circ)}{CH3 - CH - CH2 - CH2 - OH}}\\
\end{array}\]
\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{...........}\\
\ce{CH3 - C - CH2 - CH3}\\
|\phantom{............}\\
\ce{\underset{2-Methylbutan-2-ol (3^\circ)}{OH}}\phantom{.........}\
\end{array}\]
\[\begin{array}{cc}
\ce{CH3}\phantom{.......}\\
|\phantom{..........}\\
\ce{CH3 - C - CH2 - OH}\\
|\phantom{..........}\\
\ce{\underset{2, 2-Dimethylpropan-1-ol (1^\circ)}{CH3}}\phantom{......}\
\end{array}\]
\[\begin{array}{cc}
\ce{CH3}\phantom{...}\ce{OH}\phantom{.}\\
|\phantom{.........}|\phantom{...}\\
\ce{\underset{3-Methylbutan-2-ol (2^\circ)}{CH3 - CH - \underset{∗}{C}H - CH3}}\
\end{array}\]
Isomers b, d and h contain chiral carbon atoms; thus, they exhibit enantiomerism.
- Isomers a, d, e, and g are primary alcohols.
Isomers b, c and h are secondary alcohols.
Isomer f is a tertiary alcohol.
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संबंधित प्रश्न
Name the following compound according to the IUPAC system.
\[\begin{array}{cc}
\phantom{.....................................}\ce{CH2OH}\\
\phantom{............................}|\\
\ce{CH3 - CH - CH2 - CH - CH - CH3}\\
|\phantom{....................}|\phantom{............}\\
\ce{CH3}\phantom{..............}\ce{OH}\phantom{.........}\\
\end{array}\]
Write IUPAC name of the following compound:

Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - O - CH2 - CH - CH3}\\
\phantom{................}|\\
\phantom{....................}\ce{CH3}
\end{array}\]
Write structures of the compounds whose IUPAC names are as follows:
3-Chloromethylpentan-1-ol.
Give the IUPAC name of the following ether:

Natalite is a mixture of
(a) diethyl ether and methanol
(b) diethyl ether and ethanol
(c) dimethyl ether and methanol
(d) dimethyl ether and ethanol
3-Methylbutane-2-ol on heating with HI gives ______
How is phenol converted into the following?
benzoquinone
How is phenol converted into the following?
picric acid
Write IUPAC name of the following
\[\begin{array}{cc}\ce{CH3-CH-CH-CH2-OH}\\|\phantom{.....}|\phantom{.......}\\\ce{OH}\phantom{..}\ce{CH3}\phantom{.....}\end{array}\]
One of the following is not a dihydroxy derivative of benzene.
n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent?
1-Propanol and 2-propanol can be best distinguished by:
IUPAC name of the compound \[\begin{array}{cc}
\ce{CH3 - CH - OCH3}\\
\phantom{}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{..}
\end{array}\] is ______.
Assertion: Addition reaction of water to but-1-ene in acidic medium yields butan-1-ol.
Reason: Addition of water in acidic medium proceeds through the formation of primary carbocation.
Write the IUPAC name of the following compound.

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. 5-Diethylphenol
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
