17.2 Flashcards

1
Q

what are the 2 carbonyl compounds

A

aldehydes
ketones
(O=H)

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2
Q

what makes a carbonyl compound an aldehyde

A

if there is a hydrogen joined to the carbonyl group (=O is on the end on a chain)

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3
Q

what makes a carbonyl compound a ketone

A

if there are only hydrocarbon groups joined to the carbonyl group (=O is in the middle of the chain)

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4
Q

explain the polarity of carbonyl groups

A

the bond is polar because of the different electronegativities of carbon & oxygen
electron density is greater near oxygen

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5
Q

what are the physical properties of carbonyls and the difference between long & short chains

A
  • distinctive smells
    long chain - pleasant smell
    short chain - unpleasant smell
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6
Q

explain carbonyls boiling temperature

A

intermolecular forces of intermediate strength
contain polar C=O group so form permanent dipole dipole attractions but no hydrogen bonding

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7
Q

what can’t most carbonyls not form hydrogen bonds

A

because all of their hydrogen atoms are joined to a carbon and therefor get in the way

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8
Q

are carbonyls soluble in water

A

shorter chain carbonyls are soluble in water ass they can form hydrogen bonds but as they get longer the hydrocarbons become more significant & solubility decreases

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9
Q

state the oxidation & reduction products for aldehydes & ketones

A

reduction:
aldehyde -> primary alcohol
ketone -> secondary alcohol

oxidation:
aldehyde -> carbonylic acid
ketone -> not easliy oxidized

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10
Q

what reactant & conditions are needed for the reduction of carbonyls to alcohols

A

lithium aluminum hydride (lithium tertrahydridolaluminate)
LiAlH4
dissolved in dry ether

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11
Q

how are aldehydes oxidized to carboxylic acids by acidified potassium dichromate (VI)

A

orange solution -> green solution
reduction of chromium from +6 to +3 causes colour change

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12
Q

how are aldehydes oxidised to carboxylic acids by fehlings & benedicts solution

A

dark blue solution -> red precipitate
conversion of copper(II)
complex to copper (I) oxide

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13
Q

how are aldehydes oxidised to carboxylic acids by tollens reagent (ammoniacal silver nitrate)

A

colourless solution -> silver mirror
conversion of silver(I) complex to metallic silver

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