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Question
Write IUPAC names of the following

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Solution
Methoxycyclohexane
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Explain metamerism with suitable examples of ethers
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\[\begin{array}{cc}
\phantom{..................}\ce{CH2OH}\\
\phantom{.........}|\\
\ce{CH3 - CH2 - CH - CH - CH - CH3}\\
\phantom{.........}|\phantom{...................}|\\
\phantom{.............}\ce{CH2Cl}\phantom{..........}\ce{CH3}\phantom{}
\end{array}\]
Name the following compound according to the IUPAC system.
\[\begin{array}{cc}
\ce{CH3 - C = C - CH2OH}\\
|\phantom{......}|\phantom{.....}\\
\ce{CH3}\phantom{.}\ce{Br}\phantom{....}\\
\end{array}\]
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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Give IUPAC names of the following compound:

Give IUPAC names of the following compound:
\[\begin{array}{cc}
\phantom{..}\ce{H}\phantom{...}\ce{CH3}\phantom{.}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\ce{H - C - C - C - H}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{}\\
\phantom{.}\ce{H}\phantom{...}\ce{OH}\phantom{.}\ce{H}\phantom{.}\\
\end{array}\]
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When ethyl alcohol reacts with acetic acid, the products formed are:
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IUPAC name of the compound is:
\[\begin{array}{cc}
\ce{CH3-CH-OCH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]
Which of the following reagents can be used to oxidise primary alcohols to aldehydes?
(i) \[\ce{CrO3}\] in anhydrous medium.
(ii) \[\ce{KMnO4}\] in acidic medium.
(iii) Pyridinium chlorochromate.
(iv) Heat in the presence of Cu at 573 K.
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| 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 |
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Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{..............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.....}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{.}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]






