| 1. | Thus, ketones are nucleophilic at oxygen and electrophilic at carbon.
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| 2. | The ketone bodies are released by the liver into the blood.
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| 3. | Oxybenzone belongs to the class of aromatic ketones known as benzophenones.
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| 4. | Sodium borohydride reduces aldehydes and ketones to give the related alcohols.
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| 5. | Carboxylic acids react with Grignard reagents and organolithiums to form ketones.
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| 6. | Ketones can be reduced at neutral pH using the thioketal method.
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| 7. | The simple ketones include aromatic, heteroaromatic, and alkenyl ketones.
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| 8. | The simple ketones include aromatic, heteroaromatic, and alkenyl ketones.
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| 9. | Ketoses are distinguished from aldoses via their ketone / aldehyde functionality.
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| 10. | Jones reagent interacts with secondary alcohols resulting in oxidation to ketones.
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