carbonyls - aldehydes and ketones Flashcards

1
Q

aldehyde functional group and suffix

A

-al
-CHO

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2
Q

Ketone functional group and suffix

A

-one
-CO

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3
Q

Oxidation of an aldehyde
conditions + reagents + products

A

aldehyde + [O] –> Carboxylic acid

[O] = K2Cr2O7 –> Cr2O72-
Reflux

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4
Q

Oxidation of a ketones
conditions + reagents + products

A

Ketones cant undergo oxidation as they don’t have any hydrogen atoms attached to their carboxyl group

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5
Q

Whats the simple test for carbonyls also known as

A

Tollens reagent

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6
Q

How do you prepare tollens reagent

A
  1. Add AgNo3
  2. Add NaOH until Brown ppt forms
    3.Add NH4OH til colourless ( ammoniahydroxide)
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7
Q

Why can you only carry out tollens reagent on an aldehyde

A

Tollens reagent oxidises the carbonyl group and ketones don’t have nay hydrogens to be oxidised , unlike aldehydes

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8
Q

How do you use tollens reagent

If you add tollens reagent to both aldehydes and ketones what colour would you see

A

Heat gently over a waterbath

Aldehydes : silver mirror
Ketones : no colour change

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9
Q

What is the tollens reagent test use for

A

to distinguish between carbonyls

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10
Q

What does 2,4DNP /2,4DNPH stand for
what colour does it appear

A

2,4 dinitrophenylhydrazine
Green

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11
Q

What is the other name or 2,4DNP

A

Bradys reagent

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12
Q

Whats the purpose of the Bradys reagehnt test

A

To test for a carbonyl

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13
Q

What order do you carry out the test

A
  1. Bradys reagent
  2. tollens reagent
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14
Q

How do yo carry out the Bradys reagent test

A

dissolve 2,4DNP in sulfuric acid
1. React the substance with 2,4DNP ( orange colour should form)
2.Puridy by recrystallisation
3.Check the melting points against known data

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15
Q

What’s the reducing agent to reduce a carbonyl

A

NaBH4 - sodium tetrahydridoborate

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16
Q

Whats the conditions for reudcing a carbonyl

A

Room tempreature and pressure

17
Q

Reduction of an Aldehyde

A

Aldehyde + 2[H] –> primary alcohol

18
Q

Reduction of ketones

A

Ketone + 2[H] –> secondary alcohol

19
Q

Whats the mechanism for the reduction of carbonyls

A

Nucleophilic addition

20
Q

What’s the mechanism of turning a carbonyl to hydroxy nitrile
reagent
conditions
products

A

cabrobyl + CN- –> hydroxynitrile
KCN /NACN
sulphuric acid
Room temp and pressure