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Question
What is the action of hot HI on it?
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Solution
Action of hot HI on methyl n-propyl ether:

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Write the IUPAC name of the given compound:

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\[\begin{array}{cc}
\ce{CH3 - O - CH2 - CH - CH3}\\
\phantom{................}|\\
\phantom{....................}\ce{CH3}
\end{array}\]
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Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - CH2 - O - CH - CH2 - CH3}\\
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3-Chloromethylpentan-1-ol.
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(a) diethyl ether and methanol
(b) diethyl ether and ethanol
(c) dimethyl ether and methanol
(d) dimethyl ether and ethanol
How is phenol converted into the following?
benzoquinone
How do you convert the Ethanal to Propanone
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(2) formation of an ester
(3) protonation of the alcohol molecule
(4) elimination of water
What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?
Write IUPAC name of the following
\[\begin{array}{cc}\ce{CH3-CH-CH-CH2-OH}\\|\phantom{.....}|\phantom{.......}\\\ce{OH}\phantom{..}\ce{CH3}\phantom{.....}\end{array}\]
Isopropyl alcohol on oxidation forms:
C6H5OCH2CH3 is called:
Butane-2-ol is ____________.
1-Propanol and 2-propanol can be best distinguished by:
The major product formed by the reaction:
\[\begin{array}{cc}
\ce{CH3CH-CH2Br ->[CH3O^-][CH3OH] is}\\
|\phantom{................}\\
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\end{array}\]
The product of acid catalysed hydration of 2-phenylpropene is:
The correct acidic strength order of the following is:

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(II)

(III)
Give IUPAC name of the compound given below.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH - CH2 - CH2 - CH - CH3}\phantom{.}\\
\phantom{.........}|\phantom{...................}|\phantom{...........}\\
\phantom{..}\ce{Cl}\phantom{.................}\ce{OH}\phantom{..}
\end{array}\]
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(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.
Write the IUPAC name of the compound given below.
\[\begin{array}{cc}
\phantom{}\ce{CH3 - CH2 - C = C - OH}\\
\phantom{........}|\phantom{....}|\phantom{}\\
\phantom{..............}\ce{CH3 CH2OH}
\end{array}\]
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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 |
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Draw structure of the following compound.
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Write structural formulae for:
p-Nitrophenol
Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{..............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{.....}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{.}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]






