Aldehyde and Ketone Identification Quiz
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Questions and Answers

What is the general formula for ketones?

  • RCHO
  • RCOOR'
  • RCOR' (correct)
  • R(OH)R'

Which reagent is used to differentiate between aldehydes and ketones based on oxidation potential?

  • Tollen's reagent (correct)
  • 2,4-Dinitrophenylhydrazine
  • Benedict's solution
  • Chromic acid

What type of precipitate do aldehydes and ketones form when reacted with 2,4-Dinitrophenylhydrazine?

  • White
  • Colorless
  • Yellow or orange (correct)
  • Brown

What result indicates the presence of an aldehyde during Tollen's test?

<p>Formation of a silver mirror (C)</p> Signup and view all the answers

How do aldehydes differ from ketones in their chemical reactivity?

<p>Aldehydes can be easily oxidized whereas ketones cannot. (B)</p> Signup and view all the answers

What is the purpose of ammonium hydroxide in Tollen's reagent?

<p>To prevent the formation of brown silver oxide (D)</p> Signup and view all the answers

Which of the following statements about formaldehyde is true?

<p>Formaldehyde contains one hydrogen atom as the R group. (D)</p> Signup and view all the answers

Which reaction condition is necessary for the successful oxidation of aldehydes in Tollen's test?

<p>Presence of an alkaline medium (A)</p> Signup and view all the answers

What is the main distinguishing feature of aldehydes in the Fehling's test?

<p>Aldehydes reduce Fehling's reagent to give a red precipitate. (B)</p> Signup and view all the answers

Which of the following aldehydes is NOT mentioned as undergoing the Cannizzaro reaction?

<p>Acetaldehyde (B)</p> Signup and view all the answers

What color complex indicates a positive result in the sodium nitroprusside test?

<p>Red color complex (A)</p> Signup and view all the answers

What occurs during the Cannizzaro reaction?

<p>One molecule acts as the reducing agent and another as the oxidizing agent. (B)</p> Signup and view all the answers

Which of the following statements about ketones in Fehling's test is correct?

<p>Ketones do not change the color of Fehling's reagent. (D)</p> Signup and view all the answers

During the polymerization reaction, what indicates a positive result when mixing formaldehyde and resorcinol?

<p>A reddish violet color or a white ring is formed. (B)</p> Signup and view all the answers

Which of the following compounds can give a positive result in the Iodoform test?

<p>Benzyl methyl ketone (A), Acetophenone (B)</p> Signup and view all the answers

What is the expected result when benzaldehyde is reacted with concentrated hydrochloric acid after the Cannizzaro reaction?

<p>Benzoic acid is liberated as a white precipitate. (B)</p> Signup and view all the answers

Flashcards

Aldehydes

Organic compounds with the general formula RCHO, containing a carbonyl group (C=O) and a hydrogen atom or alkyl group at the carbonyl carbon.

Ketones

Organic compounds with the general formula RCOR', containing a carbonyl group (C=O) bonded to alkyl groups at the carbonyl groups.

2,4-Dinitrophenylhydrazine

A reagent used to identify aldehydes and ketones by producing a yellow or orange precipitate.

Tollen's Reagent

A reagent used to distinguish aldehydes from ketones by its ability to oxidize aldehydes. The reaction involves the reduction of silver ions to metallic silver.

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Fehling's Reagent

A reagent used to distinguish aldehydes from ketones. It oxidizes aldehydes, leading to a color change in the solution.

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Carbonyl group

A functional group consisting of a carbon atom double-bonded to an oxygen atom (C=O).

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Oxidizing agents

Chemicals that cause the oxidation of other substances to obtain a change in structure or color

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Differentiation of aldehydes and ketones

Distinguishing aldehydes and ketones by their reactivity to oxidizing agents (such as Tollens or Fehlings).

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Fehling's test

A chemical test used to distinguish aldehydes from ketones. Aldehydes reduce Fehling's reagent, a blue solution, to produce a red precipitate of cuprous oxide (Cu2O).

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Iodoform test

A test for compounds containing a terminal methyl group (–CH3). A positive test produces a yellow precipitate.

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Sodium nitroprusside test

A test for terminal methyl group-containing compounds. Sodium nitroprusside forms a red colored complex when reacting with the compounds and base, indicating a positive test.

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Cannizzaro reaction

A self-oxidation-reduction reaction of aldehydes lacking an alpha-hydrogen atom in the presence of a strong base. It yields a mixture of alcohol and the salt of the corresponding carboxylic acid.

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Polymerization reaction

A reaction where small molecules combine to form a large molecule (polymer). Formaldehyde or salicylaldehyde can react with resorcinol to produce a colored product.

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Study Notes

Aldehyde and Ketone Identification

  • Aldehydes: Compounds with the general formula RCHO. R can be aliphatic or aromatic. Formaldehyde has a hydrogen atom for R.
  • Ketones: Compounds with the general formula RCOR'. R and R' can be aliphatic or aromatic.
  • Functional Group: Both contain a carbonyl group (C=O), which is key to their chemical and physical properties. Examples of aldehydes include formaldehyde, acetaldehyde, propionaldehyde, benzaldehyde, and salicylaldehyde. Ketones include acetone, acetophenone, benzyl methyl ketone, and benzophenone.

Chemical Reactions

  • 2,4-Dinitrophenylhydrazine (2,4-DNPH) Test: Both aldehydes and ketones react with 2,4-DNPH to form a yellow or orange precipitate. This precipitate is a 2,4-dinitrophenylhydrazone.
  • General Test Procedure: Add 2-3 drops of the compound to 3 drops of the reagent. If the compound is insoluble in water, dissolve it in 1 mL of methanol first.

Differentiation Tests

  • Tollen's Test: Aldehydes react with Tollen's reagent (ammoniacal silver nitrate) to form a silver mirror (Ag). This reaction involves the oxidation of the aldehyde to a carboxylic acid.
    • Procedure: Add 2-3 drops of the compound to 2-3 mL of Tollen's reagent. Warm the test tube if no reaction occurs.
  • Fehling's Test: Only aldehydes reduce Fehling's reagent (a deep blue solution) to give a red cuprous oxide (Cuâ‚‚O) precipitate.
    • Procedure: Add 5 drops of the compound to 1 mL of Fehling’s solution and heat in a water bath for 5 minutes (shake for water insoluble compounds).
  • Important Note: Ketones do not react positively with either Tollen's or Fehling's reagent.

Special Tests for Terminal Methyl Groups

  • Iodoform Test: This test identifies aldehydes and ketones with a terminal methyl group.
  • Sodium Nitroprusside Test: Also tests for compounds with a terminal methyl group causing a red color
  • Polymerization reaction: Formaldehyde or salicylaldehyde will polymerize with resorcinol in the presence of sulfuric acid.

Cannizzaro Reaction

  • Conditions: Benzaldehyde, salicylaldehyde, and formaldehyde (no alpha-hydrogen atoms) undergo a self-oxidation-reduction reaction in a strong base (e.g., sodium hydroxide).
  • Products: The reaction produces a mixture of an alcohol and a salt of the corresponding carboxylic acid.
  • Procedure: Add a few drops of aldehyde to 0.5 mL of 30% sodium hydroxide and heat gently for 5 minutes. Then add water and concentrated hydrochloric acid for reaction confirmation.

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Description

Test your knowledge on aldehyde and ketone identification, including their structural formulas and reactions. This quiz covers essential tests like 2,4-DNPH and differentiation tests such as Tollen's Test. Perfect for chemistry students looking to strengthen their understanding of organic compounds.

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