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Oxidation of Aldehydes • Aldehydes oxidize readily to form carboxylic acids. • Ketones do not undergo oxidation. General, Organic, and Biological Chemistry: Structures of Life, 5/e © 2016 Pearson Education, Inc. Karen C. Timberlake Tollens’ Test: Silver Mirror Tollens’ test • may be used to distinguish between aldehydes and ketones. + • utilizes Tollens’ reagent, which is a solution of Ag (AgNO3) and ammonia. • oxidizes aldehydes but not ketones. • reduces Ag+, as the aldehyde is oxidized and forms a layer called a “silver mirror” on the inside of the container. General, Organic, and Biological Chemistry: Structures of Life, 5/e © 2016 Pearson Education, Inc. Karen C. Timberlake Benedict’s Test Benedict’s test • gives a positive result with compounds that have an aldehyde functional group and an adjacent hydroxyl group. • utilizes Benedict’s solution, which 2+ contains Cu (CuSO4). When the solution is added to this type of aldehyde and heated, a brick-red solid of Cu2O forms • is negative with simple aldehydes and ketones. General, Organic, and Biological Chemistry: Structures of Life, 5/e © 2016 Pearson Education, Inc. Karen C. Timberlake Benedict’s Test: 2-Hydroxy Aldehyde Because sugars such as glucose contain this type of aldehyde grouping, Benedict’s reagent can be used to determine the presence of glucose in blood or urine. General, Organic, and Biological Chemistry: Structures of Life, 5/e © 2016 Pearson Education, Inc. Karen C. Timberlake Reduction of Aldehydes and Ketones Aldehydes and ketones • are reduced by hydrogen (H ) or sodium borohydride 2 (NaBH ) and a catalyst such as nickel, platinum, or 4 palladium. • are reduced to alcohols by decreasing the number of carbon–oxygen bonds. General, Organic, and Biological Chemistry: Structures of Life, 5/e © 2016 Pearson Education, Inc. Karen C. Timberlake
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