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महाराष्ट्र राज्य शिक्षण मंडळएचएससी विज्ञान (सामान्य) इयत्ता १२ वी

Explain the following reaction: Cannizzaro reaction - Chemistry

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प्रश्न

Explain the following reaction:

Cannizzaro reaction

Explain the following reaction and write the chemical equation involved:

Cannizzaro reaction

Explain Cannizzaro reaction with suitable exnmple.

रासायनिक समीकरणे/रचना
स्पष्ट करा
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उत्तर

Aldehydes, which do not contain an α-hydrogen atom, undergo self-oxidation and reduction (disproportionation) reaction on heating with concentrated alkali (NaOH/KOH) to form an alcohol and a carboxylic acid salt.

\[\ce{\underset{Benzaldehyde}{2C6H5CHO} + NaOH -> \underset{Benzyl alcohol}{C6H5CH2OH} + \underset{Sodium benzoate}{C6H5COONa}}\]

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2021-2022 (March) Term 2 - Delhi Set 1

व्हिडिओ ट्यूटोरियलVIEW ALL [1]

संबंधित प्रश्‍न

Write a note on the self oxidation-reduction reaction of an aldehyde with a suitable example.


Write the chemical equation for the reaction involved in Cannizzaro reaction.


Write the chemical equations to illustrate the following name reaction: 

Cannizzaro’s reaction


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.


Describe the following:

Cannizzaro reaction


Write the reactions involved in the following reactions: Clemmensen reduction


Write the product(s) in the following reactions


Write the equation involved in the following reaction:

Etard reaction


Complete the following reactions:


Complete the following reactions:

 


Write the chemical equations to illustrate the following name reactions:

Aldol condensation


How will you convert acetone to acetone cyanohydrin?


Write the product formed when p-nitro chlorobenzene is heated with aqueous  NaOH at 443K followed by acidification? 


complete the following reaction: 


Complete the following reaction:


The key step in cannizzaro reaction in the inter molecular shift qf


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:


In the Cannizzaro reaction given below:

\[\ce{2Ph-CHO ->[OH^-] Ph-CH2OH + PhC\overset{-}{O}_2}\]

the slowest step is:


Which of the following does not give Cannizzaro reaction?


Convert the following:

Benzene to m-nitrobenzaldehyde


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