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प्रश्न
Show how you would synthesise the following alcohol from an appropriate alkene?
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उत्तर
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संबंधित प्रश्न
Name the reagents used in the following reactions:
How do you convert the following : Propan-2-ol to 2-methylpropan-2-ol
Show how is the following alcohol prepared by the reaction of a suitable Grignard reagent on methanal?
Predict the major product of acid catalysed dehydration of butan-1-ol.
How is the following conversion carried out?
\[\ce{Benzyl chloride -> Benzyl alcohol}\]
Name the reagent used in the following reaction:
Butan-2-one to butan-2-ol.
Write the structures of A, B and C in the following reactions :
Primary alcohols are prepared by the reduction of carboxylic acids. Though lithium aluminium hydride is a strong reducing agent, it is not used in the reaction. This is so because:
Monochlorination of toluene in sunlight followed by hydrolysis by aq. \[\ce{NaOH}\] yields.
Which of the following reacts with NaOH to give alcohol?
Commercially carboxylic acids are reduced to alcohols by converting them to the ______.
Acetone reacts with Grignard reagent to form:
Carboxylic acids are more acidic than phenol and alcohol because of
Most readily hydrolysed halide is:-
When alcohol react with concentrated H2SO4 intermediate compound formed is
Glycerol is used in the manufacture
When glycol is heated with dicorboxylic acid the product are
Alkaline hydrolysis of an alkyl halide can be preferably carried out using ______.
The major product of the following reaction is:
\[\begin{array}{cc}
\ce{Cl}\phantom{.........................}\\
|\phantom{..........................}\\
\ce{CH3 - CH - CH3 ->[(i) Alc. KOH][(ii) HBr/peroxide (iii) aq. KOH]}
\end{array}\]
How are the following conversion carried out?
\[\ce{Methyl magnesium bromide -> 2-Methylpropan-2-ol}\]
