Advertisements
Advertisements
प्रश्न
How is the following conversion carried out?
\[\ce{Benzyl chloride -> Benzyl alcohol}\]
Advertisements
उत्तर १
If benzyl chloride is treated with NaOH (followed by acidification), then benzyl alcohol is produced.

उत्तर २

APPEARS IN
संबंधित प्रश्न
Name the reagents used in the following reactions:

Write the main product(s) in each of the following reactions:

Name the reagents used in the following reactions:

Write the structures of the main products when acetone (CH3 − CO − CH3) reacts with the following reagents :
CH3MgBr and then H3O+
Predict the major product of acid catalysed dehydration of butan-1-ol.
How is the following conversion carried out?
\[\ce{Methyl magnesium bromide -> 2-Methylpropan-2-ol}\]
Name the reagent used in the following reaction:
Dehydration of propan-2-ol to propene.
Name the reagent used in the following reaction:
Butan-2-one to butan-2-ol.
Show how you would synthesise the following alcohol from an appropriate alkene?

Name the reagents used 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:
Commercially carboxylic acids are reduced to alcohols by converting them to the ______.
Acetone reacts with Grignard reagent to form:
The Wittig reaction is a reaction between a carbonyl compound (aldehyde or ketone only) and a species known as a phosphoniumylide. What is the expected final product in the Wittig reaction?
A compound does not react with 2, 4 dinitrophenylhydrazine, the compound is:
The major product of acid catalysed dehydration of 1-methylcyclohexanol is ______.
To synthesise 1.0 mole of 2-methylpropan-2-ol from Ethylethanoate ______ equivalents of CH3MgBr reagent will be required. (Integer value)


The products "A" and "B" formed in above reactions are:
The major product of the following reaction is:
\[\begin{array}{cc}
\ce{Cl}\phantom{.........................}\\
|\phantom{..........................}\\
\ce{CH3 - CH - CH3 ->[(i) Alc. KOH][(ii) HBr/peroxide (iii) aq. KOH]}
\end{array}\]
