Identifying Aldehydes Flashcards

1
Q

What is Tollens’ reagent composed of?

A

Silver(1) ions, Ag* (aq), in the presence of ammonia

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2
Q

What role do silver ions play in the reaction with aldehydes?

A

Oxidising agent

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3
Q

What is produced when silver ions are reduced during the reaction with aldehydes?

A

Silver

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4
Q

What happens to the aldehyde when it reacts with Tollens’ reagent?

A

Oxidised to a carboxylic acid

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5
Q

What is the indication of a positive Tollens’ test?

A

Formation of a silver mirror

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6
Q

What precipitate forms during the 2,4-DNP test?

A

2,4-dinitrophenylhydrazone precipitate

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7
Q

How is the solid precipitate from the 2,4-DNP test processed?

A

Recrystallised to produce a pure sample of crystals

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8
Q

What is the next step after obtaining the pure sample of 2,4-DNP?

A

Measure and record the melting point

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9
Q

What should the melting point be compared to for identification purposes?

A

A database or data table of melting points

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10
Q

How can you distinguish between aldehydes and ketones after identifying a carbonyl group?

A

Using Tollens’ reagent

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11
Q

What is the visual result of an aldehyde reacting with Tollens’ reagent?

A

Silver mirror forms

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12
Q

What happens if a ketone is tested with Tollens’ reagent?

A

No reaction is observed

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13
Q

Describe the preparation method for Tollens’ reagent.

A

Add silver nitrate to sodium hydroxide until brown precipitate forms, then add dilute ammonia until it dissolves

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14
Q

Fill in the blank: Tollens’ reagent should be prepared immediately before carrying out the test because it has a _______.

A

Short shelf-life

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15
Q

What is the first step in testing an unknown solution with Tollens’ reagent?

A

Pour 2cm depth of the unknown solution into a clean test tube

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16
Q

What temperature should the test tube with Tollens’ reagent be placed in for the reaction?

A

About 50°C

17
Q

Which carbonyl compound would produce a silver mirror with Tollens’ reagent?

18
Q

Write the general equation for the reaction of an aldehyde with Tollens’ reagent.

A

RCHO + 2Ag^+ + 2OH^- → RCOO^- + 2Ag + 2H2O