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Write a reaction for the following conversion. Benzene to Benzaldehyde. - Chemistry

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प्रश्न

Write a reaction for the following conversion.

Benzene to Benzaldehyde.

Convert benzene into benzaldehyde.

रासायनिक समीकरण/संरचनाएँ
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उत्तर

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अध्याय 12: Aldehydes, Ketones and Carboxylic acids - Short answer questions (Type-II)

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एससीईआरटी महाराष्ट्र Chemistry [English] 12 Standard HSC
अध्याय 12 Aldehydes, Ketones and Carboxylic acids
Short answer questions (Type-II) | Q 3.1

वीडियो ट्यूटोरियलVIEW ALL [2]

संबंधित प्रश्न

Write the structures of A and B in the following reactions:


Write the structure of the product of the following reaction:

\[\ce{H3C - C ≡ C - H ->[Hg^{2+}, H2SO4]}\]


Complete the synthesis by giving missing starting material, reagent or product.


Complete the synthesis by giving missing starting material, reagent or product.


Write a note on ‘aldol condensation’.


What is the action of phenyl hydrazine on propanone?


What is the action of Zn – Hg / conc. HCl on propanone?


What is the action of Sodium bisulphite on propanone?


Write only reactions for the preparation of benzophenone from benzonitrile.


Write chemical equation for the following:
Gatterman - Koch formylation


Write the IUPAC name of the follow

\[\begin{array}\ce{\phantom{--..}O}\\\ce{\phantom{--..}||}\\ \ce{CH2=CH-C-CH3}\end{array}\]


Write chemical equation for the following :
Rosenmund reduction


How will you convert calcium acetate to acetaldehyde?


Complete the following reaction:
\[\ce{(C6H5CH2)2Cd + 2CH3COCI}\]


Answer the following in one sentence.

Write reaction showing conversion of ethanenitrile into ethanol.


Answer the following in one sentence.

Predict the product of the following reaction:

\[\ce{CH3 - CH2 - COOCH3->[i) AIH(i-Bu)_2][ii) H3O+]}\]?


What is the action of following reagents on ethanoic acid?

SOCl2/heat


Draw structure of salicylaldehyde.


The formation of aldehyde from an alkyl cyanide using SnCl2/conc.HCl is known as ____________.


Catalyst used in Rosenmund reduction is ____________.


Which of the following is a Stephen reaction?


Identify the compound obtained by side chain chlorination of toluene and hydrolysed further.


The reaction in which methyl group on benzene ring is converted to aldehydic group is called ______.


The product of the reaction between dimethylcadmium and acetyl chloride is ____________.


Identify the compound A and Bin following reaction.

\[\ce{CH3Cl ->[KCN(alc)][\Delta] A ->[2H2O][HCl] B + NH4Cl}\]


Identify 'A' in the following reaction:

\[\begin{array}{cc}
\phantom{...........}\ce{O}\\
\phantom{...........}||\\
\ce{2A + (C6H5CH2)2 Cd -> 2CH3 - C - CH2 - C6H5 + CdCl2}\end{array}\]


Which of the following compounds does NOT undergo Friedel-Crafts reaction?


Identify 'A' in the following reaction.

\[\ce{A ->[H2][Pd-BaSO4] C6H5CHO + HCl}\]


Chromyl chloride converts methyl group to a chromium complex, which on acid hydrolysis gives corresponding aldehyde. This reaction is called ____________.


Given below are two statements labelled as Assertion (A) and Reason (R).

Assertion (A): SO2 is reducing while TeO2 is an oxidising agent.

Reason (R): Reducing property of dioxide decreases from SO2 to TeO2.

Select the most appropriate answer from the options given below:


Which of the following reaction is shown by alkynes?


Which of the following on heating with aqueous KOH, produces acetaldehyde?


Which reagent is used in Etard reaction?


What is the action of hydrogen cyanide on the following?

Benzaldehyde


How butanone is prepared from alcohol?


How are the following compound obtained by hydration of alkenes?

Ethyl alcohol


How are the following compound obtained by hydration of alkenes?

Isopropyl alcohol


Explain Rosenmund reduction reaction.


Write the name of the product formed when ethanoyl chloride is treated with dimethyl cadmium.


How acetone is prepared from nitriles using Grignard reagent?


Write preparation of propanone by using ethanoyl chloride and dimethyl cadmium.


Which of the following on heating with aqueous KOH produces acetaldehyde.


Identify the suitable reagent for the following conversion.


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