Advertisements
Advertisements
Question
How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
Methyl benzoate
Advertisements
Solution
APPEARS IN
RELATED QUESTIONS
On acid hydrolysis, propane nitrile gives.
Write the structures of A and B in the following reactions
Predict the products of the following reactions:
Show how the following compound can be converted to benzoic acid.
Ethylbenzene
Show how the following compound can be converted to benzoic acid.
Acetophenone
Show how the following compound can be converted to benzoic acid.
Phenylethene (Styrene)
Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagent.
Tollens’ reagent
An organic compound (A) (molecular formula C8H16O2) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and an alcohol (C). Oxidation of (C) with chromic acid produced (B). (C) on dehydration gives but-1-ene. Write equations for the reactions involved.
How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
m-Nitrobenzoic acid
How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
p-Nitrobenzoic acid
Complete the synthesis by giving missing starting material, reagent or product.
How is methoxy benzene prepared from carbolic acid?
Which is the most suitable reagent for the following conversion?
\[\begin{array}{cc}
\phantom{....................}\ce{O}\phantom{.....................................}\ce{O}\phantom{.}\\
\phantom{....................}||\phantom{......................................}||\phantom{.}\\
\phantom{}\ce{CH3 - CH = CH - CH2 - C - CH3 -> CH3 - CH = CH - CH2 - C - OH}\phantom{.}
\end{array}\]
Assertion: Aldehydes and ketones, both react with Tollen’s reagent to form silver mirror.
Reason: Both, aldehydes and ketones contain a carbonyl group.
The end product Y in the sequence of reaction:
\[\ce{RX ->[CN^-] X ->[NaOH] Y}\] is:
Y is:
Alkaline hydrolysis of C4H8Cl2 gives a compound (A) which on heating with NaOH and I2 produces a yellow precipitate of CHI3. The compound (A) should be ______.
