Praktikum Kimia Organik : Identifikasi Gugus Karbonil pada Aldehid dan Keton

FIK UMMAT
16 Jul 202010:48

Summary

TLDRThis video demonstrates various chemical tests to identify aldehyde and ketone groups in different compounds. It covers three main tests: the Benedict, Tollens, and Fehling reactions. The results show how glucose and lactose (which contain aldehyde groups) react positively with all three tests, producing color changes or precipitates. In contrast, acetone (a ketone) does not react, as it requires stronger oxidizers. The video highlights the differences in reactivity between aldehydes and ketones, explaining how specific reagents target aldehyde groups, resulting in distinctive visual changes.

Takeaways

  • πŸ˜€ The experiment aims to distinguish between carbonyl group reactions in aldehydes and ketones.
  • πŸ˜€ In the Benedict test, glucose and lactose showed a positive reaction with a brick red color change, while acetone did not react.
  • πŸ˜€ Benedict reagent contains copper(II) ions, which can reduce to copper(I) in the presence of aldehydes but not ketones.
  • πŸ˜€ In the Tollens test, glucose and lactose showed silver sediment formation, indicating a positive reaction with aldehydes, while acetone showed no reaction.
  • πŸ˜€ Tollens reagent can oxidize aldehydes into carboxylic acids and produce a silver mirror effect, but ketones do not react.
  • πŸ˜€ The Fehling test showed a positive reaction with glucose and lactose, as evidenced by a brick red precipitate, while acetone did not react.
  • πŸ˜€ The brick red color in the Fehling test indicates the presence of aldehyde groups, which can be oxidized during the reaction.
  • πŸ˜€ The absence of a reaction in acetone during the Fehling test is because ketones do not reduce copper(II) ions.
  • πŸ˜€ The heating process in all tests aims to accelerate the oxidation reactions involving aldehydes but not ketones.
  • πŸ˜€ Ketones like acetone can only react with strong oxidants like potassium permanganate, unlike aldehydes that can react with weaker oxidants like Benedict and Tollens reagents.

Q & A

  • What is the primary purpose of the experiment described in the video?

    -The primary purpose of the experiment is to recognize and distinguish carbon group reactions, specifically the reactions of carbonyl groups in aldehyde and ketone compounds.

  • What is the first test conducted in the experiment, and what does it involve?

    -The first test conducted is the Benedict test. In this test, three test tubes are filled with acetone, glucose, and lactose. Benedict's reagent is added, and the tubes are heated to observe the color change.

  • What does a positive result in the Benedict test indicate?

    -A positive result in the Benedict test is indicated by a color change to brick red in the glucose and lactose solutions, signaling the reduction of copper 2 ions to copper ions.

  • Why did acetone show no color change in the Benedict test?

    -Acetone showed no color change because Benedict's reagent contains CO2 ions, which are weak oxidants. These oxidants can only oxidize aldehyde groups, not ketone groups like acetone.

  • What does the Tollens test aim to detect, and how does it work?

    -The Tollens test aims to detect aldehyde groups. When an aldehyde reacts with Tollens reagent and is heated, the aldehyde is oxidized to a carboxylic acid, and the Tollens reagent is reduced, forming silver metal that precipitates as a mirror on the test tube.

  • What was the result of the Tollens test with glucose and lactose?

    -The result of the Tollens test with glucose and lactose was a positive reaction, with silver sediment forming, indicating the presence of aldehyde groups.

  • Why did acetone show no reaction with Tollens reagent?

    -Acetone showed no reaction with Tollens reagent because acetone is a ketone, and ketones cannot be oxidized by the weak oxidizing agents in Tollens reagent. Only aldehydes are reactive in this test.

  • What is the role of heat in the Benedict and Tollens tests?

    -Heat is used in both the Benedict and Tollens tests to accelerate the chemical reactions, facilitating the color changes and the formation of precipitates, which indicate the presence of aldehyde groups.

  • How does the Fehling's test work, and what was observed in this experiment?

    -The Fehling's test involves adding Fehling's reagent to the sample and heating it. In the experiment, a positive result was indicated by a brick red precipitate in the glucose and lactose samples, which contain aldehyde groups. There was no reaction in acetone because ketones do not react with Fehling's reagent.

  • Why does acetone not react in the Fehling's test?

    -Acetone does not react in the Fehling's test because ketones, like acetone, cannot be oxidized by Fehling's reagent. The reagent only reacts with aldehyde groups, which have a hydrogen atom directly attached to the carbonyl carbon.

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Related Tags
Carbonyl ReactionsAldehydesKetonesBenedict TestTollens TestFehling TestOrganic ChemistryChemical ReactionsLab ExperimentsThailand