Reactions of carbonyls Flashcards

1
Q

Functional group of carbonyls

A

-c=o

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2
Q

types of carbonyls

A

aldehyde and ketone

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3
Q

difference between aldehyde and ketone

A
  • In aldeHYDES the functional group is terminal

- In ketones the functional group can be found within the compound

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4
Q

naming aldehyde

A

alkylnal

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5
Q

naming ketone

A

alkanone

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6
Q

Why are aldehydes more reactive than ketones

A

They have less electron donating R groups which makes the Carbonyl C more positive hence more likely to undergo nucleophilic attack

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7
Q

formation of Aldehyde

A

Oxidation of primary alcohol

  • KMnO4/ KCr2O7
  • distill
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8
Q

Formation of Ketone

A

Oxidation of secondary alcohol

  • acidified KCr2O7
  • reflux
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9
Q

Carbonyl to Alcohol

A

Reduction
-LiAlH4 or NaBH4 or H2 + Ni catalyst

  • in dry ether
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10
Q

carbonyl to carboxylic acid

A

acidified KMnO4
heat/reflux
(ketone does not undergo oxidation)

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11
Q

carbonyl to nitrile

A

HCN + NaCN catalyst

cold

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12
Q

Test for carbonyls

A

2,4-DNPH
warm
orange ppt
condensation reaction

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13
Q

Iodoform reaction

A

-aqeous iodine and NaOH
warm
yellow CHI3 Crystal’s formed

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14
Q

Test for Carbonyls(Fehling’s)

A

Aldehyde
- deep blue to red orange
(except benzaldehyde)

Ketone
- remains deep blue

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15
Q

Testing for Carbonyls (Tollen’s)

A

aldehyde
- colorless grey ppt

ketones
- no reaction remains colorless

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16
Q

What is fehling’s solution made of?

A

Cu2+

17
Q

What is Tollens reagent made of?

A

Ag(NH3)2^+