Advertisements
Advertisements
प्रश्न
How will you prepare cinnamic acid from benzaldehyde?
Advertisements
उत्तर
Conversion of benzaldehyde into cinnamic acid:
\[\begin{array}{cc}
\phantom{....}\ce{COOH}\phantom{...............}\ce{COOH}\phantom{......}\\
\phantom{....}/\phantom{.....................}/\phantom{.............}\\
\ce{\underset{(Benzaldehyde)}{C6H5CH = O} + H2C ->[Pyridine][-H2O] C6H5CH = C ->[\Delta][-CO2] \underset{(Cinnamic acid)}{C6H5CH = CH} - COOH}\\
\phantom{....}\backslash\phantom{.....................}\backslash\phantom{.............}\\
\phantom{}\ce{\underset{(Malonic acid)}{COOH}}\phantom{.............}\ce{COOH}\phantom{....}
\end{array}\]
APPEARS IN
संबंधित प्रश्न
_____________ reaction is used to synthesize straight alkyl substituted benzenes.
Ethyl methyl ketone can be reduced to n-butane by which of the following reactions?
In Clemmensen's reaction, ketone gives ____________.
Which of the following carbonyl compounds does NOT undergo aldol condensation?
Which of the following is Clemmensen reduction?
Predict the product Z in the following series of reactions.
\[\ce{Ethanoic acid ->[PCl5] X ->[C6H6][Anhydrous AlCl3] Y ->[i) CH3MgBr][H3O^+] Z}\]
Identify the product formed in the reaction.

Assertion: p-N, N-dimethyl amino benzaldehyde undergoes benzoin condensation
Reason: The aldehydic (−CHO) group is meta directing.
Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.
Write the structure of the major product of the aldol condensation of benzaldehyde with acetone.
