Isomers Flashcards

1
Q

What are isomers?

A

Compounds that have the same molecular formula but a different arrangement of atoms.

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

What are structural isomers?

A

Compounds that have the same molecular formula but different structural formulae.

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

What are the three types of structural isomerism?

A
  • Functional group isomerism
  • Positional isomerism
  • Branched chain isomerism
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What causes functional group isomerism?

A

Different functional groups result in the same molecular formula.

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

Give examples of homologous series that can be functional group isomers.

A
  • Alkenes and cycloalkanes
  • Alcohols and ethers
  • Aldehydes and ketones
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is positional isomerism?

A

Isomers that arise from differences in the position of a functional group in each isomer.

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

What is the primary alcohol butan-1-ol’s functional group position?

A

Attached to carbon-1.

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

What is the secondary alcohol butan-2-ol’s functional group position?

A

Attached to carbon-2.

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

What is branched chain isomerism?

A

When compounds have the same molecular formula, but their longest hydrocarbon chain is not the same.

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

How are amines classified?

A

Based on the number of alkyl groups attached to the nitrogen in the amine.

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

Define primary amines.

A

Amines where the nitrogen is attached to one other carbon atom.

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

Define secondary amines.

A

Amines where the nitrogen is attached to two other carbon atoms.

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

Define tertiary amines.

A

Amines where the nitrogen is attached to three other carbon atoms.

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

What are stereoisomers?

A

Isomers that have the same order of atoms but different spatial arrangements.

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

What are conformational isomers?

A

Isomers that occur due to free rotation about a single σ-bond.

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

What is a staggered conformer?

A

A conformer where hydrogen atoms on adjacent carbons have angles of 60 degrees.

17
Q

Why is the eclipsed conformer less stable?

A

Due to repulsion between the electrons in the C-H bonds that are closer together.

18
Q

What is configurational isomerism?

A

Isomerism seen in unsaturated compounds or compounds with at least one asymmetric carbon.

19
Q

What are cis/trans isomers?

A

Isomers that differ in the position of functional groups relative to a double bond or ring.

20
Q

What are the characteristics of cis isomers?

A

Functional groups are on the same side of the double bond or carbon ring.

21
Q

What are trans isomers?

A

Functional groups are on opposite sides of the double bond or carbon ring.

22
Q

What is a racemic mixture?

A

A mixture containing equal amounts of each enantiomer.

23
Q

Why is a racemic mixture optically inactive?

A

The enantiomers cancel out each other’s effect on polarized light.

24
Q

What is an enantiomer?

A

A pair of optical isomers that are mirror images of each other.

25
How do enantiomers differ chemically?
They interact differently with biological sensors.
26
What is a primary alcohol?
An alcohol where the functional group carbon is attached to one other carbon atom.
27
What is the relationship between enantiomers and optical activity?
One enantiomer rotates plane polarized light clockwise, the other anticlockwise.
28
What is the significance of chiral centers in optical isomers?
A chiral carbon has four different atoms or groups attached, leading to enantiomers.
29
What are diastereomers?
Compounds that contain more than one chiral centre and are not mirror images.