[3.3.11] Amines Flashcards

Preparation, Base Properties & Nucleophilic Properties.,

1
Q

How do you name amines?

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

Name these two molecules.

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

Name these three molecules.

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

Name this molecule.

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

Describe the base strength of primary aliphatic amines.

Explain the difference in base strength of primary aliphatic amines compared to ammonia.

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

Describe the base strength of secondary aliphatic amines.

Explain the difference in base strength between secondary aliphatic amines and primary aliphatic amines.

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

Describe the base strength of aromatic amines.

Explain the difference in base strength of aromatic amines compared to aliphatic amines.

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

What is the overall order of base strength of amines?

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

When amines react with acids, what product is formed?

Write an equation for the reaction between methylamine and hydrochloric acid.

What can you add to the product of this reaction to convert it back to the amine?

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

Write equations for the reactions between:

  • Methylamine and H+
  • Diethylamine and H+
  • Triethylamine and H+

(The H+ coming from an acid)

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

How do you make a basic buffer solution from an amine?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe and explain the issue in forming a primary amine by the reaction of ammonia with a halogenoalkane.

What solution is there to this issue?

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

How can primary amines be formed and through what mechanism are they formed?

A
  • Primary amines can be formed by the nucleophilic substitution reaction between halogenoalkanes and ammonia in a one-step reaction.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

STEP 1

Write the overall equation for the reaction between ammonia and bromoethane.

Draw the mechanism for this reaction.

STEP 2

Draw the mechanism for the reaction between the product produced in step 1 and bromoethane.

What type of product is produced, name it.

STEP 3

Draw the mechanism for the reaction between the product produced in step 2 and bromoethane.

What type of product is produced, name it.

STEP 4

Draw the mechanism for the reaction between the product produced in step 3 and bromoethane.

What type of product is produced, name it.

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

If you used an excess of halogenoalkane with ammonia, what would predominately be produced?

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

Draw a diagram to represent the overall scheme of reactions that occur when a halogenoalkane reacts with ammonia.

Use “RX” to represent the halogenoalkane.

17
Q

What can quaternary ammonium salts be used as?

Why can they be utilised like this?

18
Q

Draw the structure of all the products formed when bromomethane reacts with propylamine.

Name all the products

19
Q

Describe how you can prepare amines from nitriles.

What are the advantages and disadvantages of this?

20
Q

Using bromoethane as a starting product, write equations to show how you can form a primary amine by reacting bromoethane with a nitrile.

21
Q

Describe the reagent, conditions and mechanism to form aromatic amines from nitroarenes.

Draw the overall equation for this reaction where the nitroarene is nitrobenzene.

22
Q

What is the change in the functional group, reagents and conditions when ethanoyl chloride reacts with methylamine?

Draw the structural and displayed formulae for this reaction.

23
Q

What is the change in the functional group, reagents and conditions when ethanoic anhydride reacts with methylamine?

Draw the structural and displayed formulae for this reaction.