10 Questions
Reduction of carboxylic acids can directly produce aldehydes
False
Primary alcohols can be oxidized to aldehydes using pyridinium dichromate (PDC) or pyridinium chlorochromate (PCC)
True
Aldehydes can be prepared by reducing acyl chlorides
True
Oxidation of tertiary alcohols gives aldehydes.
False
Reduction of esters directly produces carboxylic acids
False
Synthesis of aldehydes from nitriles involves oxidation reactions
False
Reduction of ketones gives secondary alcohols.
False
Reduction of aldehydes gives primary alcohols.
True
Ozonolysis of di-substituted alkene will give one molecule of ketone and one molecule of aldehyde.
True
2-Butene upon ozonolysis gives only ethanol.
False
Learn how aldehydes are synthesized by oxidizing 1o (primary) alcohols using pyridinium dichromate (PDC) or pyridinium chlorochromate (PCC) in anhydrous media, without over oxidation to carboxylic acids. Explore the oxidation of primary alcohols to aldehydes and the reduction of Acyl chlorides, esters, and more.
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