17b - Carbonyl Compounds Flashcards

1
Q

Bonding in carbonyls

A
  • Can form London forces and Permanent dipole-dipole interactions
  • Cannot form hydrogen bonds with each other
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2
Q

Solubility of carbonyls

A
  • lower carbonyls can form hydrogen bonds with water so they are soluble to some extent
  • Solubility decreases as chain length increases as the hydrocarbon part becomes more significant
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3
Q

Aldehyde + Fehling’s solution

A
  • Deep blue solution -> red precipitate
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4
Q

Aldehyde + acidified potassium dichromate

A
  • orange to green as Cr becomes reduced
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5
Q

Aldehyde + Tollens’ reagent

A
  • Colourless –> silver mirror
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6
Q

Aldehyde + LiAlH4 (dry ether)

A
  • Primary alcohol is formed
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7
Q

Ketone + LiAlH4 (dry ether)

A
  • Secondary Alcohol is formed
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8
Q

In equations what are oxidising agents and reducing agents represented as?

A
  • Oxidising : [O]

- Reducing : [H]

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9
Q

What does the Iodine in presence of reaction with carbonyl compounds show?

A
  • Presence of a (CH3CO) group

- can give false results as some alcohols contain CH3COH which can react

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10
Q

What is the qualitative test for a carbonyl compound? and how can we identify the compund?

A
  • 2,4-DNPH
  • Dry the derivative and measure its melting temperature
  • Compare with data book values
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11
Q

Why when you add KCN in the presence of HCN it would produce a racemic mixture? (Nucleophilic addition)

A
  • Forms a racemic mixture as the C=O is planar and can be attacked from both sides
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