Podcast
Play an AI-generated podcast conversation about this lesson
Questions and Answers
Reduction of carboxylic acids can directly produce aldehydes
Reduction of carboxylic acids can directly produce aldehydes
False (B)
Primary alcohols can be oxidized to aldehydes using pyridinium dichromate (PDC) or pyridinium chlorochromate (PCC)
Primary alcohols can be oxidized to aldehydes using pyridinium dichromate (PDC) or pyridinium chlorochromate (PCC)
True (A)
Aldehydes can be prepared by reducing acyl chlorides
Aldehydes can be prepared by reducing acyl chlorides
True (A)
Oxidation of tertiary alcohols gives aldehydes.
Oxidation of tertiary alcohols gives aldehydes.
Signup and view all the answers
Reduction of esters directly produces carboxylic acids
Reduction of esters directly produces carboxylic acids
Signup and view all the answers
Synthesis of aldehydes from nitriles involves oxidation reactions
Synthesis of aldehydes from nitriles involves oxidation reactions
Signup and view all the answers
Reduction of ketones gives secondary alcohols.
Reduction of ketones gives secondary alcohols.
Signup and view all the answers
Reduction of aldehydes gives primary alcohols.
Reduction of aldehydes gives primary alcohols.
Signup and view all the answers
Ozonolysis of di-substituted alkene will give one molecule of ketone and one molecule of aldehyde.
Ozonolysis of di-substituted alkene will give one molecule of ketone and one molecule of aldehyde.
Signup and view all the answers
2-Butene upon ozonolysis gives only ethanol.
2-Butene upon ozonolysis gives only ethanol.
Signup and view all the answers
