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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
i. The isomeric alcohols with molecular formula C5H12O are –
(a) \[\ce{\underset{Pentanol (1^\circ)}{CH3 - CH2 - CH2 - CH2 - CH2 - OH}}\]
(b) \[\begin{array}{cc}
\ce{CH3 - CH2 - CH2 - \overset{∗}{C}H - CH3}\\
\phantom{............}|\\
\phantom{...............}\ce{\underset{Pentan-2-ol (2^\circ)}{OH}}\
\end{array}\]
(c) \[\begin{array}{cc}
\ce{CH3 - CH2 - CH - CH2 - CH3}\\
|\phantom{..}\\
\phantom{..}\ce{\underset{Pentan-3-ol (2^\circ)}{OH}}\
\end{array}\]
(d) \[\begin{array}{cc}
\ce{H3C - H2C - H\overset{∗}{C} - CH2OH}\\
\phantom{.....}|\\
\phantom{.........}\ce{\underset{2-Methylbutan-1-ol (1^\circ)}{CH3}}\
\end{array}\]
(e) \[\begin{array}{cc}
\ce{CH3}\phantom{............}\\
|\phantom{...............}\\
\ce{\underset{3-Methylbutan-1-ol (1^\circ)}{CH3 - CH - CH2 - CH2 - OH}}\\
\end{array}\]
(f) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3 - C - CH2 - CH3}\\
|\phantom{.......}\\
\ce{\underset{2-Methylbutan-2-ol (3^\circ)}{OH}}\phantom{....}\
\end{array}\]
(g) \[\begin{array}{cc}
\ce{CH3}\phantom{...}\\
|\phantom{......}\\
\ce{CH3 - C - CH2 - OH}\\
|\phantom{......}\\
\ce{\underset{2, 2-Dimethylpropan-1-ol (1^\circ)}{CH3}}\phantom{..}\
\end{array}\]
(h) \[\begin{array}{cc}
\phantom{.}\ce{CH3}\phantom{...}\ce{OH}\\
|\phantom{......}|\phantom{..}\\
\ce{\underset{3-Methylbutan-2-ol (2^\circ)}{CH3 - CH - \underset{∗}{C}H - CH3}}\
\end{array}\]
Isomers (b), (d) and (h) contain chiral carbon atoms; thus, they exhibit enantiomerism.
ii. 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
Write IUPAC name of the following compound:
C6H5 – O – C7H15(n−)
What is the action of hot HI on it?
How is phenol converted into the following?
Benzene
Write structural formula for Methyl vinyl ether.
An example of a compound with functional group – O – is ____________.
Ethylene reacts with Baeyer’s reagent to give ______.
Match the starting materials given in Column I with the products formed by these (Column II) in the reaction with HI.
| Column I | Column II | ||
| (i) | CH3—O—CH3 | (a) | ![]() |
| (ii) | \[\begin{array}{cc} \ce{CH3}\phantom{..................}\\ \backslash\phantom{.............}\\ \ce{CH-O-CH3}\\ /\phantom{..............}\\ \ce{CH3}\phantom{..................} \end{array}\] |
(b) | \[\begin{array}{cc} \ce{CH3}\phantom{....}\\ |\phantom{.......}\\ \ce{CH3-C-I + CH3OH}\\ |\phantom{.......}\\ \ce{CH3}\phantom{....} \end{array}\] |
| (iii) | \[\begin{array}{cc} \ce{CH3}\phantom{.}\\ |\phantom{....}\\ \ce{H3C-C-O-CH3}\\ |\phantom{....}\\ \ce{CH3}\phantom{..} \end{array}\] |
(c) | ![]() |
| (iv) | ![]() |
(d) | CH3—OH + CH3—I |
| (e) | \[\begin{array}{cc} \ce{CH3}\phantom{.....................}\\ \backslash\phantom{.................}\\ \ce{CH-OH + CH3I}\\ /\phantom{.................}\\ \ce{CH3}\phantom{.....................} \end{array}\] |
||
| (f) | \[\begin{array}{cc} \ce{CH3}\phantom{.....................}\\ \backslash\phantom{.................}\\ \ce{CH-I + CH3OH}\\ /\phantom{.................}\\ \ce{CH3}\phantom{.....................} \end{array}\] |
||
| (g) | \[\begin{array}{cc} \ce{CH3}\phantom{....}\\ |\phantom{.......}\\ \ce{CH3-C-OH + CH3I}\\ |\phantom{.......}\\ \ce{CH3}\phantom{....} \end{array}\] |
Assertion: p-nitrophenol is more acidic than phenol.
Reason: Nitro group helps in the stabilisation of the phenoxide ion by dispersal of negative charge due to resonance.
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.
Write the IUPAC name of the following compound.

Write a chemical reaction for the following conversion:
Acetic acid into ethyl alcohol.
How are the following conversions carried out?
Methyl magnesium bromide→2-Methylpropan-2-ol.
Draw structure of the following compound.
2-Methoxypropane
Draw structure of the following compound.
Prop-2-en-1-ol
Write structural formulae for:
p-Nitrophenol
Write structural formulae for:
Salicylic acid
The IUPAC name of
is ______.
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{..}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]



