Cyclic hemiacetals commonly form if a molecule has both an alcohol group and a carbonyl group elsewhere in the same molecule, especially if they are four or five carbons apart. What is the structure of the hydroxy aldehyde from which this hemiacetal might form?
Aldosterone is a key steroid involved in controlling the sodium–potassium balance in the body. Identify the functional groups in aldosterone.

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What two products result from the complete hydrolysis of this cyclic acetal?
Acetals and ketals are usually made by reaction of an aldehyde or ketone with two molecules of a monoalcohol. If an aldehyde or ketone reacts with one molecule of a dialcohol, however, a cyclic acetal or ketal results.
b. Draw the cyclic ketal formed when the hemiketal from part (a) reacts with the ―OH labeled in blue.
The compound carvone is responsible for the odor of spearmint. Identify the functional groups in carvone.
Can the alcohol (CH3)3COH be formed by the reduction of an aldehyde or ketone? Why or why not?
Many flavorings and perfumes are partially based on fragrant ketones, with far fewer being based on fragrant aldehydes. Why do you think ketones are used more frequently than aldehydes? See Section 15.5 for a clue.
