1.carbonylys acids and esters Flashcards

1
Q

what is a carbonyl compound?

A

a keytone or a aldehyde

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what kind of reaction does a carbonyl bond tend to undergo? (C=O)

A

neucleophillic addition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is the neucleophile in the neucleophilic addiditon of a carbonly bond?

A

H-

from NaBH4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

mechanism for the neucleophillic addition of a carbonyl compound?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what oxidising agent fo you use?

A

Cr2O72-/H+

acidified dicramate ions

K2Cr2O7/H+

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

form a keytone?

A

secondary alcohol

reflux

acidified dicromate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

form an aldehyde?

A

primary alcohol

acidified dicromate in 1:1 ratio

add [0] to alcohol drop wise

distil as it forms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Equation for the reduction of ethanal to ethanol

A

CH3CHO + 2[H] —> CH3CH2OH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

WHat is tollens reagent?

A

ammonical silver nitrate solution

A silver mirror is formed upon the addition of an aldehyde

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

possitive test for tollens?

A

SIlver mirror in aldehyde presence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

how to make tollens reagent?

A
  1. Silver nitrate + NaOH (brown precip AgOH formed)
  2. Add enough NH3 to remove the precipitate as it becomes a complex ion.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Tollens reagent reaction?

A

Aldehyde + [O] —> Carboxilic acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What does 2,4-DNPH test for?

A

aldehydes and keytones

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is 2,4-DNPH solution

A

its an orange solution that when mixed with methanol and sulfuric acid becomes the oxidising agent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

2,4-DNPH stands for?

A

2,4-dinitrophenylhydrazine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

positive test for 2,4-DNPH?

A

an orange or yellow precipitate called 2,4-DNPH derivitive is formed.

17
Q

What can the 2,4-DNPH derivitie be used for?

A
  • identifying the carbonyl compound
  • First Filter and recrystalize it to purify it
  • find the melting point of the crystals
  • compare this to a database to identify the compound.
18
Q

2,4-DNPH reaction?

A

The H2 from the hydrazine section of 2,4-DNPH is lost , as well as the O on the carbonly they formm water.

The other two form a hydrozone.

19
Q

What kinds of carboxilic acid are water soluble and why?

A
  • Chains between 1-4 carbons
  • the polar end of the acid makes up a large proportion, this can hydrogen bond witht he water
20
Q

Esterification reaction

A

Alcohol + Carboxylic acid —> ester +water reflux, conc sulfuric acid catalyst,warm.

21
Q

Making an ester from an anhydride and its benifits?

A

Anhydride + methanol–> ester + carboxillic acid

heat

Better yield then other method

22
Q

Define Hydrolysis

A

Is a draction with water or hyroxide ions that breaks a chemical compound into two compounds

23
Q

Acid Hydrolysis of an ester

A

Ester heated under refulx with dilute sulfuric acid (or dilute HCL) with water

Forms alcohol and a carboxillic acid

24
Q

Alkali Hydrolisis of an ester?

A

AQUEOUS Sodium/potassium hydroxide is refulxed with the ester

forms metal salt of carboxillic acid and an alcohol.

25
Q

Uses of esters?

A
  • Perfumes
  • Flavourings
26
Q

name of a metal carboxillic acid salt?

A

metal <chain>anoate known as carboxylates</chain>

eg sodium methanoate

27
Q

Why do carboxillic acids dissociate more then alcohols?

A

The -COO- is more stable then -CO-

this is due to the charge being distributed across more atoms

28
Q

Making biodiesel?

A

triglyceride + 3 alcohol (short chain) —> glyserol + 3 ester

NaOH catlyst

29
Q

Elimination of H2O from alcohol.

A