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प्रश्न
Give IUPAC name of the following ether:
\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{CH3}
\end{array}\]
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उत्तर
1-Ethoxy-2-methylpropane
APPEARS IN
संबंधित प्रश्न
Write the IUPAC name of the given compound:
Name the following compound according to IUPAC system.
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
\phantom{}|\phantom{.............}|\phantom{......}|\phantom{.........}\\
\phantom{}\ce{OH}\phantom{..........}\ce{OH}\phantom{...}\ce{C2H5}\phantom{......}
\end{array}\]
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - O - CH2 - CH - CH3}\\
\phantom{..........}|\\
\phantom{............}\ce{CH3}
\end{array}\]
Give IUPAC name of the following ether:
O2N – C6H4 – OCH3(p)
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
Which of the following compounds is NOT prepared by the action of alcoholic NI3 on alkyl halide?
(a) CH3NH2
(b) CH3- CH2- NH2
(c) CH3 - CH2 - CH2 - NH2
(d) (CH3)3 C- NH2
How is phenol converted into the following?
Benzene
How is phenol converted into the following?
benzoquinone
Write structural formulae for 1-Ethylcyclohexanol.
Write structural formulae for Cyclohex-2-en-1-ol.
One of the following is not a dihydroxy derivative of benzene.
An example of a compound with functional group – O – is ____________.
HBr reacts fastest with ____________.
When ethyl alcohol reacts with acetic acid, the products formed are:
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.
Explain why Lewis acid is not required in bromination of phenol?
Write a chemical reaction for the following conversion:
Acetic acid into ethyl alcohol.
Write structural formulae for:
p-Nitrophenol
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
