6.1.2 - Carbonyl Compounds Flashcards

1
Q

What is the carbonyl group?

A

C=O

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2
Q

What is the functional group
and general formula for an
aldehyde?

A

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

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3
Q

What is the functional group
for a ketone?

A

RCOR’ (C double bonded to O)

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4
Q

How do you name
aldehydes?

A

-al suffix (C=O is on the end of a chain)

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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 the
carbonyl group have? Why?

A

Permanent dipole-dipole due to the polar C=O
bond (O is ∂-)

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7
Q

How soluble are carbonyls 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 the polarity of the bond (large
difference in electronegativity between C and O)

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9
Q

What is the strongest bond
in carbonyl compounds?

A

C=O

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10
Q

Why is the 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 the product of HCN
added to a carbonyl
compound 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
enantiomers.

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12
Q

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

A

Hydroxynitriles (have OH and CN groups)

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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 compound?

A

Use Brady’s reagent -
2,4-dinitrophenylhydrazine
If a carbonyl compound is present an orange
precipitate is formed

17
Q

How do you test for a
carbonyl compound?

A

Use Brady’s reagent -
2,4-dinitrophenylhydrazine
If a carbonyl compound is present an orange
precipitate is formed

18
Q

What is in Tollens’ reagent?

A

Silver complex ions in colourless solution

19
Q

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

A

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

20
Q

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

A

No visible change

21
Q

What is another oxidising
agent for alcohols and
aldehydes? What change in
colour does this undergo?

A

Acidified potassium dichromate (VI) - H₂SO₄
and
K₂Cr₂O₇.
Colour change from orange to green.

22
Q

What is a reducing agent for
aldehydes and ketones?
What ions does this release
in solution?

A

NaBH4
(sodium tetrahydridoborate (III)),
releases an H-
ion

23
Q

Write an equation for the
reduction of pentan-2-one
and for 3-methylbutanal.

A

CH₃COCH₂CH₂CH₃ + 2[H] → CH₃CH(OH)CH₂CH₂CH₃

CH₃CH₂CH₂(CH₃)CHO + 2[H] → CH₃CH₂CH₂(CH₃)CH₂OH

24
Q

How do you convert an
aldehyde to form a
carboxylic acid?

A

Oxidation of aldehydes using Cr₂O₇ (2-) / H+
(i.e. ₂2Cr₂O₇ / H₂SO₄)