Physical World
Ketones $$[ R-\underset{O}{\underset{||}{C}}-R']$$ where, $$R={ R }^{ \prime }=$$ alkyl group can be obtained in one step by :
The most suitable reagent for the conversion of $$ R-CH_{2}-OH\rightarrow R-CHO$$ is :
The most suitable reagent for the conversion of $$ R-CH_{2}-OH\rightarrow R-CHO$$ is $$PCC$$ (Pyridinium Chlorochromate).
Primary alcohols are oxidized to aldehydes. Aldehydes are further oxidized to carboxylic acids.
$$PCC$$ (Pyridinium Chlorochromate) is a mild oxidizing agent. it oxidizes primary alcohols to aldehydes only. The further oxidation to carboxylic acid does not occur.
$$CrO_{3}$$, $$KMnO_{4}$$ and $$K_{2}Cr_{2}O_{7}$$ are strong oxidizing agents. They oxidize primary alcohol to aldehdye and further to carboxylic acid.
Ketones $$[ R-\underset{O}{\underset{||}{C}}-R']$$ where, $$R={ R }^{ \prime }=$$ alkyl group can be obtained in one step by :
How will you bring about the following conversions in not more than two steps ? Ethanol to 3-Hydroxybutanal
Suggest a reagent for the following conversion:
Complete the reaction.
Ketones, where, R & R' are alkyl groups can be obtained in one step by:
The most suitable reagent for the conversion of primary alcohol into aldehyde with the same number of carbon is:
The compound on dehydrogenation gives a ketone. The original compound is:
Which is oxidized most easily?
Product $$(P)$$ is :
Encircle whichever of the following: