Linked from

The 62 pages that link to Carbonyl group, each with the reason it gives.

• Maillard reactionRelated: The carbonyl group in a reducing sugar reacts with amino groups in the early stages.

• EsterificationRelated: The carboxylic acid’s carbonyl carbon is the site where the new ester linkage forms.

• UreaRelated: Its carbonyl group defines the central unit in urea’s structure.

• TautomerismRelated: Carbonyl compounds commonly form enol tautomers by moving an adjacent proton.

• Sugar alcoholRelated: Reduction of this group converts a sugar into its corresponding sugar alcohol.

• TransesterificationRelated: The ester carbonyl carbon is the reaction site attacked by the incoming alcohol.

• Hydration reactionRelated: Water can add to carbonyl compounds to form geminal diols.

• Acetyl groupRelated: Its polarized C=O bond gives the acetyl carbon its characteristic reactivity.

• QuinoneRelated: Two carbonyl groups are defining structural features of quinones.

• Hydride transferRelated: Its polarized bond makes the carbon atom a common target for hydride.

• Acetic anhydrideRelated: Its two carbonyl groups make the anhydride susceptible to nucleophilic attack.

• Addition reactionRelated: Its polarized double bond makes carbonyl compounds susceptible to nucleophilic addition.

• GlyceraldehydeRelated: Glyceraldehyde’s open-chain form has a terminal aldehyde carbonyl.

• Acetyl chlorideRelated: Its polarized carbonyl bond makes acetyl chloride’s acyl carbon susceptible to attack.

• DihydroxyacetoneRelated: Its ketone carbonyl distinguishes dihydroxyacetone from its aldose isomer.

• FormamideRelated: Its carbonyl carbon is bonded directly to nitrogen in formamide.

• GlycolaldehydeRelated: This group forms the aldehyde end of glycolaldehyde.

• AcetamideRelated: Acetamide’s carbonyl carbon is bonded to both methyl and amino groups.

• ChloralRelated: Chloral’s carbonyl carbon is the site of its characteristic addition reactions.

• Glyoxylic acidRelated: Glyoxylic acid contains carbonyl groups in both its aldehyde and carboxylic acid functionality.