9) Unit 2 - Sterochemistry Flashcards

1
Q

What is an isomer

A

molecules that have the same molecular formula but differ in the way their atoms are arranged

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

what are the 2 types of isomers

A
  • structural isomers

* stereoisomers

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

describe a structural isomer

A

atoms are bonded together in a different order in each isomer

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

describe stereoisomer

A

atoms are bonded in the same order, but the arrangement of atoms in space is different for each isomer

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

Name the two types of stereoisomers

A
  • geometric

* optical

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

when does geometric isomerism occur

A
  • in molecules with a c=c bond, with each carbon having 2 different groups attached to it
  • in cycloalkanes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what does cis and trans mean in geometric isomers with c=c bonding

A
cis = when two groups are on the same side
trans = when groups are on opposite sides
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what does cis and trans mean in geometric isomers with saturated rings (cycloalkanes)

A
cis = when 2 groups are on the same side of the plane
trans = when 2 groups are on opposite sides of the plane
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are optical isomers and where do they occur

A
  • asymmetrical molecules that are non-superimposable mirror images of each other
  • exist in compounds with a chiral carbon atom (1 carbon bonded to 4 different groups)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How are optical isomers different

A

optical isomers are identical in every physical property except their effect on plane polarised light
They can be identified as R or S.

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

how is light deflected in a:

100% R-isomer

A

100% to the right

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

how is light deflected in a:

100% S-isomer

A

!00% to the left

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

how is light reflected in a:

70% R and 30% S isomer

A

40% to the right

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

How is light deflected in a:

20% R and 80% S isomer

A

60% to the left

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

•How is light deflected in a:

50% R and 50% S isomer

•And what is this called

A
  • there is no deflection

* this mixture is called a race mixture

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

How are optical isomers present in biological systems and give 2 examples

A

They are usually chiral but only present in one of their optical forms. e.g. amino acids, enzymes