6.1.2 Carbonyl Compounds Flashcards

1
Q

What is the carbonyl group?

A

C=O

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2
Q

What is functional group and general formula for an aldehyde?

A

RCHO (C=O, single bonded to H and R)

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3
Q

What is functional group for a ketone?

A

RCOR’ (C=O)

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4
Q

How do you name aldehydes?

A

-al suffix

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5
Q

How do you name ketones?

A
  • one suffix (designate number for which carbon C=O is on)
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6
Q

What kind of intermolecular forces do molecules with carbonyl group have? Why?

A

Permanent dipole-dipole due to polar C=O bond

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7
Q

How soluble are they in water? What influences solubility?

A

Yes- form hydrogen bonds between water molecules and oxygen of C=O. As C chain length increases, solubility decreases.

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8
Q

Which bond in carbonyl compounds is usually involved in reactions? Why?

A

C=O, due to polarity of bond

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9
Q

What is strongest bond in carbonyls?

A

C=O

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10
Q

Why is addition of HCN important?

A

Increases the length of the carbon chain by one carbon atom allowing more useful molecules to be made.

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11
Q

Will product of HCN added to a carbonyl have optical isomers? Why?

A

Yes they will. In the aldehyde/ ketone, the carbonyl carbon is planar, so the :CN- can attack from either above or below forming two enatiomers

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12
Q

What is name of product when HCN is added to a carbonyl?

A

Hydroxynitriles

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13
Q

What is Fehling’s solution? What colour is it?

A

Copper complex ions, blue

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14
Q

What happens when an aldehyde is added to Fehling’s solution?

A

Reduced to Cu+ ions -> colour change to brick red ppt

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15
Q

What happens when a ketone is added to Fehling’s solution?

A

No visible change -> stays blue

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16
Q

How do you test for a carbonyl?

A

Use 2,4-DNP
If a carbonyl is present an orange precipitate is formed

17
Q

What is in Tollen’s reagent?

A

Silver complex ions in colourless solution

18
Q

What happens when an aldehyde is added to Tollen’s reagent?

A

Silver mirror forms as Ag+ reduced to Ag (s)

19
Q

What happens when a ketone is added to Tollen’s reagent?

A

No visible change

20
Q

What is a reducing agent for carbonyls?

A

NaBH4- releases H- ions

21
Q

How do you convert aldehyde to form carboxylic acid?

A

Oxidation using Cr2O7 ^2-/ H+