Advertisements
Advertisements
प्रश्न
Write the structure of main compounds A and B in the following reaction:
\[\ce{CH3CH2CN->[CH3MgBRH/3O+]A->[LiAIH4]B}\]
Advertisements
उत्तर
\[\begin{array}{cc}
\phantom{.........}\ce{O}\\
\phantom{.........}||\\
\ce{CH3CH2CN->[CH3MgBr/H3O+] CH3-C\underset{\text{A}}{H2}-C-CH3->[LiAIH4]CH3CH2\underset{\text{B}}{C}HCH3}
\end{array}\]
APPEARS IN
संबंधित प्रश्न
Predict the major product of acid catalysed dehydration of butan-1-ol.
How is the following conversion carried out?
\[\ce{Propene -> Propan-2-ol}\]
How is the following conversion carried out?
\[\ce{Methyl magnesium bromide -> 2-Methylpropan-2-ol}\]
Aldehydes react with Grignard reagent to produce ____________.
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.
Select the acid(s) which cannot be prepared by Grignard reagent.
Carboxylic acids are more acidic than phenol and alcohol because of
When alcohol react with concentrated H2SO4 intermediate compound formed is


The products "A" and "B" formed in above reactions are:
