| 1. | In this case an intramolecular OH group reacts with the carbonyl group.
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| 2. | In many nucleophilic reactions, addition to the carbonyl group is very important.
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| 3. | The position of the carbonyl group is usually denoted by a number.
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| 4. | Finally, deprotonation of the oxygen of the carbonyl group produces the ester.
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| 5. | The following figure shows a ligated metal attached to a carbonyl group.
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| 6. | In this reaction the carbonyl group is an aldehyde or a ketone.
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| 7. | Overall, the carbonyl group is oxidized, and the hydrogen peroxide is reduced.
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| 8. | Its reactions with nucleophiles often involves the reaction of both carbonyl groups.
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| 9. | Burgi-Dunitz trajectoryThe nucleophilic attack on the carbonyl group proceeds via B�rgi-Dunitz trajectory.
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| 10. | This makes the carbonyl group more susceptible to attack by the peroxyacid.
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