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

APPEARS IN
RELATED QUESTIONS
Explain metamerism with suitable examples of ethers
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 the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
|\phantom{....................}|\phantom{.........}|\phantom{.............}\\
\ce{OH}\phantom{................}\ce{OH}\phantom{...}\ce{C{_2}H5}\phantom{.........}\\
\end{array}\]
Write the IUPAC name of the following compound:

Write IUPAC name of the following compound:

Give the IUPAC name of the following ether:

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
How is phenol converted into the following?
Benzene
How is phenol converted into the following?
benzoquinone
Write the IUPAC name of the following compound:

Write the IUPAC name of the following :

Resorcinol on distillation with zinc dust gives _________.
Write IUPAC names of the following

3-methylphenol is called ____________.
The compound HOCH2 – CH2OH is __________.
An example of a compound with functional group – O – is ____________.
Ethyl alcohol is industrially prepared from ethylene by:
The product of acid catalysed hydration of 2-phenylpropene is:
Which of the following gives a positive iodoform test?
The correct acidic strength order of the following is:

(I)

(II)

(III)
Explain why p-nitrophenol is more acidic than phenol.
Assertion: Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.
Reason: Lewis acid polarises the bromine molecule.
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.
Draw structure of the following compound.
2. 5-Diethylphenol
Draw structure of the following compound.
Prop-2-en-1-ol
Write structural formulae for:
p-Nitrophenol
Write the IUPAC name.
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C -CH3}\\
\phantom{.}|\phantom{......}|\phantom{......}|\\
\phantom{....}\ce{CH3\phantom{...}\ce{OH}\phantom{...}\ce{CH3}}\
\end{array}\]
