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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

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-Nitrobenzaldehyde - Chemistry

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प्रश्न

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-Nitrobenzaldehyde

रासायनिक समीकरणे/रचना

उत्तर

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पाठ 12: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ ३७८]

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एनसीईआरटी Chemistry [English] Class 12
पाठ 12 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 14.5 | पृष्ठ ३७८

संबंधित प्रश्‍न

Write the chemical equations to illustrate the following name reactions : Rosenmund reduction


Predict the product of the following reaction:


Write the reaction involved in the Stephen reduction


Ozonolysis of alkenes followed by the reaction with zinc dust and water gives ____________ depending on the substitution pattern of the alkene.


Aldehydes are prepared by reducing nitriles to corresponding imines with stannous chloride in the presence of hydrochloric acid. This reaction is called:


The oxidation of toluene to benzoic acid can be done using which of the following reagents.


Name the electrophile produced in the reaction of benzene with benzoyl chloride in the presence of anhydrous \[\ce{AlCl3}\]. Name the reaction also.


Can Gatterman-Koch reaction be considered similar to Friedel Craft’s acylation? Discuss.


The strongest base among the following


When 2 – hydroxyl benzoic acid distilled with zinc dust, it give


Aldehydes are the first oxidation products of ______.


The oxidation of toluene to benzaldehyde by chromyl chloride is called ______.


Explain the following reactions:

Stephan reaction


Predict the reagent for carrying out the following transformations:

Benzoyl chloride to Benzaldehyde


The reaction of benzene with CO and HCl in the presence of anhydrous AlCl3 gives ______.


Write the name of the reaction, structure and IUPAC name of the product formed when:

CH3CH2CN reacts with stannous chloride in the presence of hydrochloric acid, followed by hydrolysis.


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