32 Flashcards

1
Q

Name

A

Aldehydes

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2
Q

Name

A

Ketones

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3
Q

What are carbonyl (oxo) compounds

A

These molecules possess a C=O atomic group

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4
Q

What are ketones?

A

carbonyl group bonded to

two carbons in the carbon skeleton

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5
Q

What are aldehydes

A

oxo group attached to terminal carbon

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6
Q

Identify the compound

A

Carboxylic acid

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7
Q

Identify the compound

A

Esters

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8
Q

Identify the compound

A

Acid halides

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9
Q

Identify the compound

A

Amides

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10
Q

Identify the compound

A

Formaldehyde (methanal)

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11
Q

Identify the compound

A

Acetaldehyde (ethanal)

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12
Q

Identify the compound

A

Propionaldehyde (propanal)

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13
Q

Identify the compound

A

Butyraldehyde (butanal)

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14
Q

Identify the compound

A

Benzaldehyde

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15
Q

Identify the compound

A

4-methylpentanal

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16
Q

Identify the compound

A

2-ethylpentanal

17
Q

3 examples of Biologically important, naturally occurring oxo compounds

18
Q

Examples of nucleobases that are ketones

A

N-containing, heterocyclic aromatic compounds; substituted purine or pyrimidine rings

19
Q

Example of Oxo-enol tautomerism of the nucleobases

A

Oxo form is the most stable

20
Q

Physical properties of carbonyl compounds

-> Do aldehydes or ketones forms H-bonds? Why?

A

Neither aldehydes nor ketones possess the ability to form H-bonds as there are no O – H sigma bonds in the molecules.

21
Q

Compare the boiling points of carbonyl compounds to that of alcohols

A

boiling points for aldehydes and ketones are lower than for alcohols of similar molar mass.

22
Q

Compare the boiling points of carbonyl compounds to that of alkanes

A

As a result of dipole-dipole interactions, their boiling points are higher than for alkanes of similar molar mass.

23
Q

Describe Water solubility of carbonyl compounds

A

The carbonyl group oxygen atom is a hydrogen bond acceptor, so short-chain aldehydes and ketones are water-soluble

(Greater carbon length makes the molecule less polar and less water-soluble)

24
Q
Synthesis of oxo compounds by
mild oxidation (dehydrogenation) of alcohols (reactions, products)
25
Chemical reactions of carbonyl compounds
26
Oxidation of aldehydes
27
Oxidation of kenos
28
Describe Reduction to the corresponding alcohol
29
Nucleophilic addition (AN) reactions: hydration under alkalic conditions
30
Describe hemiacetal formation
31
formation of hemi)ketals
32
Describe Schiff base (imine) formation