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What is the difference between an aldehyde and a ketone, and how can you distinguish between the two using chemical reactions or tests? Provide specific examples and explain the underlying chemical principles involved.

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Aldehydes and ketones are both organic compounds containing a carbonyl group  C=O . The main difference between them lies in the position of the carbonyl group and the types of atoms bonded to the carbonyl carbon.In an aldehyde, the carbonyl group is located at the end of a carbon chain, and the carbonyl carbon is bonded to a hydrogen atom and an alkyl group  or a hydrogen atom in the case of formaldehyde . The general formula for an aldehyde is RCHO, where R represents an alkyl group or a hydrogen atom.In a ketone, the carbonyl group is located within the carbon chain, and the carbonyl carbon is bonded to two alkyl groups  or aryl groups . The general formula for a ketone is RCOR', where R and R' represent alkyl or aryl groups.To distinguish between aldehydes and ketones, several chemical reactions or tests can be used:1. Tollens' test: This test uses Tollens' reagent, which is an ammoniacal silver nitrate solution. When an aldehyde is added to Tollens' reagent, it gets oxidized to a carboxylic acid, and the silver ions in the reagent are reduced to metallic silver, forming a silver mirror on the inner surface of the test tube. Ketones do not react with Tollens' reagent, as they are not easily oxidized. This test is based on the oxidation of aldehydes and the reduction of silver ions.2. Fehling's test: Fehling's test uses Fehling's solution, which is a mixture of copper II  sulfate, potassium sodium tartrate, and sodium hydroxide. When an aldehyde is added to Fehling's solution, it gets oxidized to a carboxylic acid, and the copper II  ions in the solution are reduced to copper I  oxide, forming a reddish-brown precipitate. Ketones do not react with Fehling's solution, as they are not easily oxidized. This test is based on the oxidation of aldehydes and the reduction of copper II  ions.3. Schiff's test: This test uses Schiff's reagent, which is a solution of fuchsin dye decolorized by the addition of sulfurous acid. When an aldehyde is added to Schiff's reagent, it reacts with the sulfurous acid to form a colored complex, turning the solution pink or magenta. Ketones do not react with Schiff's reagent. This test is based on the formation of a colored complex between aldehydes and the decolorized fuchsin dye.4. Iodoform test: This test is specific for methyl ketones, which have a CH3COR structure. When a methyl ketone is treated with iodine and a base  such as sodium hydroxide , it forms a yellow precipitate of iodoform  CHI3 . Most aldehydes do not give a positive iodoform test, except for acetaldehyde, which also forms iodoform under these conditions. This test is based on the halogenation and subsequent hydrolysis of methyl ketones to form iodoform.In summary, aldehydes and ketones differ in the position of the carbonyl group and the types of atoms bonded to the carbonyl carbon. Various chemical tests, such as Tollens' test, Fehling's test, Schiff's test, and the iodoform test, can be used to distinguish between them based on their reactivity and the formation of specific products.

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