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Ch 12 Aldehydes and Ketones Naming and Properties Carbonyl Functional Group • oxygen video Aldehydes • Functional group is a carbonyl group bonded to an end-standing Carbon (#1) • Condensed structural formula is indicated as – CHO (COH is alcohol) Ketones • Carbonyl group is bonded to a central carbon of a parent alkane or a ring Aldehyde Naming CH3 CH3 – CH2 – CH – CH2 – CH2 – C – H 1. Find longest C-chain containing carbonyl group 2. Name: drop the alkane‘e’ replace with ‘-al’ : hexanal 3. In aldehydes, carbonyl is always C#1 – no number needed – implied in aldehyde name! 4. Locate/list other substituents: 4-methylhexanal Ketone Naming –CO– Cl CH3 – CH – C – CH2 – CH2 – CH3 1. Find longest C-chain containing carbonyl group 2. Name: drop alkane ‘e’ replace with ‘-one’ hexanone 3. Number: Carbonyl gets lowest possible number 3hexanone ( longer ketones need location number for carbonyl) 4. Locate/list other substituents in front 2-chloro-3-hexanone Complex molecules with everything….. • Use substituent name carbonyl (list alpha under C) Properties of Aldehydes & Ketones • intermolecular forces of Carbonyls 1. Dipoles 2. Van der Waals – depending on Carbon chain length • Length of Carbon chain • C1-C2 gas, C3 -C10: liquid, C11 and higher: solids Melting and Boiling Points • Aldehydes/ketones have BP between alkanes and alcohols, close to ethers • Intermolecular forces: Dipoles and Van-der-Waals, but no H-Bonds with each other!!!! Solubility • Aldehydes and ketones with 4 or less carbons are very soluble in water • Carbonyl can H-bond with water Rx of Aldehydes and Ketones Oxidation of Aldehydes • Aldehydes can be oxidized • Visible as addition of Oxygen aldehyde carboxylic acid Oxidation of Ketones • Ketones cannot be oxidized!!! • No H that can be removed • No O can be added Benedict’s Test • [O] + Cu2+ +O2 → Glucose + Cu2O Gluconic Acid Sequential Oxidation of Carbon Compounds Purpose: gradual release of chemical bond energy that can be captured (ATP) instead of a quick combustion that produces mostly heat, light (useless for the body) alkane→ 1° alcohol → aldehyde→carboxylate→ CO2 alkane →2o alcohol →ketone → Ø Branched alkane → 3o alcohol → Ø • agains the grain