Preparation of Aldehydes and Ketones

IMPORTANT

Preparation of Aldehydes and Ketones: Overview

This topic covers concepts such as Methods of Preparation of Aldehydes and Ketones, Preparation of Aldehydes and Ketones by Oxidation of Alcohols, Preparation of Aldehyde and Ketones by Dehydrogenation of Primary and Secondary Alcohols, etc.

Important Questions on Preparation of Aldehydes and Ketones

EASY
IMPORTANT

The reagents used for the following conversions are:

(i) cyclohexanol to cyclohexan-1-one           

(ii) bromobenzene to benzoic acid

MEDIUM
IMPORTANT

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

HARD
IMPORTANT

1-methylcyclohexa-1, 3-diene on reductive ozonolysis with Zn/H2O yields products A and B.The total number of sp2 hybridized carbons in A and B are

EASY
IMPORTANT

The Aldehyde prepared from nitro alkane starts with _____.

EASY
IMPORTANT

How the alkenes are the substrate and CO/H2 are the reagent of oxo process.

EASY
IMPORTANT

Write the oxo process to produce aldehydes?

MEDIUM
IMPORTANT

Write a chemical reaction for the oxo process.

EASY
IMPORTANT

Oxo process is an industrial process to prepare the ketone.

MEDIUM
IMPORTANT

Complete the following reaction: 

C6H5CH3 + CrO3 acetic anhydride ?

MEDIUM
IMPORTANT

Which of the following is not synthesized by Rosenmund reduction:

EASY
IMPORTANT

Ethyl methyl ketone is obtained by heating calcium salts of

HARD
IMPORTANT

The Grignard's reagent used to convert Benzonitrile to acetophenone (benzophenone) is:

EASY
IMPORTANT

In the following reaction, P gives two products Q and R each in 40% yield.

Question Image

If the reaction is carried out with 420 mg of P, the reaction yields 108.8 mg of Q. The amount of R produced in the reaction is closest to

MEDIUM
IMPORTANT

The major product of the following reaction. 

Question Image is

MEDIUM
IMPORTANT

Benzene reacts with acetyl chloride in the presence of anhydrous AlCl3, we get Aceto_____ as the product.

HARD
IMPORTANT

What are A and B in the following reaction sequence?
Propionitrile +ABH3O propiophenone