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प्रश्न
Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.
(A) formaldehyde
(B) acetaldehyde
(C) acetone
(D) ethyl methyl ketone
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उत्तर
(B) acetaldehyde
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संबंधित प्रश्न
Name the following compound according to the IUPAC system.

Write the IUPAC name of the following compound:
\[\begin{array}{cc}
\ce{CH3 - CH2 - O - CH - CH2 - CH3}\\
\phantom{....}|\\
\phantom{........}\ce{CH3}
\end{array}\]
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Give the IUPAC name of the following ether:

Write the structure and IUPAC name of 'methyl-n-propyl ether'.
What is the action of hot HI on it?
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picric acid
Write IUPAC name of the following compound (CH3)2 N − CH2CH3
Write the structures of the products when Butan-2-ol reacts with SOCl2
Resorcinol on distillation with zinc dust gives _________.
Write structural formulae for 1-Ethylcyclohexanol.
Ethyl alcohol is industrially prepared from ethylene by:
Ethylene reacts with Baeyer’s reagent to give ______.
The product of acid catalysed hydration of 2-phenylpropene is:
The heating of phenyl methyl ether with HI produces:
Among the following sets of reactants which one produces anisole?
IUPAC name of the compound \[\begin{array}{cc}
\ce{CH3 - CH - OCH3}\\
\phantom{}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{..}
\end{array}\] is ______.
Which of the following reagents can be used to oxidise primary alcohols to aldehydes?
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(iii) Pyridinium chlorochromate.
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\[\ce{H2O, ROH, HC ≡ CH}\]
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Write complete reaction for the bromination of phenol in aqueous and non-aqueous medium.
Identify A and B in the following:

Draw structure of the following compound.
2-Methoxypropane
Draw structure of the following compound.
Prop-2-en-1-ol
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{...............}\ce{CH3}\\
\phantom{............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
Write IUPAC name of the following compound:
\[\begin{array}{cc}
\phantom{................}\ce{CH3}\\
\phantom{.............}|\\
\ce{CH3 - CH - CH - C - CH3}\\
|\phantom{......}|\phantom{......}|\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{CH3}
\end{array}\]
