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Question
Write the product formed when p-nitro chlorobenzene is heated with aqueous NaOH at 443K followed by acidification?
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Solution
RELATED QUESTIONS
Complete the following reactions:
An organic compound with the molecular formula C9H10O forms 2, 4-DNP derivative, reduces Tollens’ reagent and undergoes Cannizzaro reaction. On vigorous oxidation, it gives 1, 2-benzenedicarboxylic acid. Identify the compound.
Write the product(s) in the following reactions
Complete the following reactions:
Complete the following reactions:
Complete the following reaction:
Explain the following reaction:
Cannizzaro reaction
What happens when methanal undergoes cannizzaro reaction?
\[\begin{array}{cc}
\ce{D}\phantom{........................}\\
|\phantom{.........................}\\
\ce{2D - C = O + OH^- ->[Cannizzaro] X and Y}
\end{array}\]
(Y is alcohol, D is deuterium)
X and Y will have the structure:
Benzaldehyde can be prepared by the hydrolysis of:
