4.4 Nomenclature and isomerism Flashcards

1
Q

What are Positional Isomers?

A

Molecules with the same molecular formula but have the functional group on a different position in the molecule.

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2
Q

What are Functional Group Isomers?

A

Molecules with the same molecular formula, but different functional groups.

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3
Q

Name the three different types of Structural Isomers:

A
  • Chain Isomers
  • Positional Isomers
  • Functional Group Isomers
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4
Q

What are Stereoisomers?

A

Molecules that have the same structural formula but a different arrangement of atoms in space.

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5
Q

Name the two different types of Stereoisomers:

A
  • E/Z Isomers

- Optical Isomers

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6
Q

What is the cause of E/Z isomerism?

A

Restricted rotation around the C=C Double bond

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7
Q

What name is given to a carbon atom that is bonded to four different atoms, or groups?

A

Chiral or asymmetric carbon

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8
Q

What is a Chiral/Asymmetric Carbon?

A

A carbon atom that is bonded to four different atoms, or groups.

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9
Q

When do Optical Isomers occur?

A

When a molecule contains a Chiral/Asymmetric carbon atom

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10
Q

Define Optical Isomers:

A

Molecules that contain a chiral/asymmetric carbon and exist as non super-imposable mirror images.

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11
Q

What is the name for two optical isomers?

A

A pair of enantiomers

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12
Q

How do you distinguish between two enantiomers?

A

They have opposite rotation of plane polarised light

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13
Q

What is a racemate or racemic mixture?

A

A mixture containing equal amounts of each enantiomers

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14
Q

Why are racemates/racemic mixtures not optically active?

A

Because the effects cancel each other out because there is an equal amount of each enantiomer

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15
Q

Why is it important to test the effects of both enantiomers of an optically active drug during drug trials?

A

Because in some optical isomers, one enantiomer is an effective drug, whilst the other may have toxic or harmful side effects e.g. Thalidomide

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16
Q

What is the functional group for the homologous series: Nitriles

A

R - C (Triple Bond) H

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17
Q

What is the functional group for the homologous series: Amines

A

R - N - H
|
H

18
Q

What is the functional group for the homologous series: Esters

A

O
||
R - C - O - R

19
Q

What is the functional group for the homologous series: Amide

A
O
       ||
R - C - N - H
              |
             H
20
Q

What is the functional group for the homologous series: Acyl Chloride

A

O
||
R - C - Cl

21
Q

What are Chain Isomers?

A

Molecules with the same molecular formula, but a different arrangement of carbon atoms.

22
Q

What is the functional group for the homologous series: Acid Anhydride

A

O O
|| ||
R - C - O - C - R

23
Q

What is the functional group for the homologous series: Arenes

24
Q

What is the functional group for the homologous series: Alcohols

25
What is the functional group for the homologous series: Aldehydes
R = O | H
26
What is the functional group for the homologous series: Ketones
O || R - C - R
27
What is the functional group for the homologous series: Carboxylic Acids
O || R - C - O - H
28
What is the prefix for the homologous series: Amines
Amino-
29
What is the prefix for the homologous series: Alcohols
Hydroxy-
30
What is the suffix for the homologous series: Nitriles
-Nitrile
31
What is the suffix for the homologous series: Amines
-amine
32
What is the suffix for the homologous series: Esters
-oate
33
What is the suffix for the homologous series: Amide
-amide
34
What is the suffix for the homologous series: Acyl Chloride
-oyl Chloride
35
What is the suffix for the homologous series: Acid Anhydride
-ic Anhydride
36
What is the suffix for the homologous series: Arenes
-benzene
37
What is the suffix for the homologous series: Alcohols
-ol
38
What is the suffix for the homologous series: Aldehydes
-al
39
What is the suffix for the homologous series: Ketones
-one
40
What is the suffix for the homologous series: Carboxylic Acids
-oic Acid
41
Name the type of steroisomerism shown by 2-chloro butane and give the meaning of the term racemic mixture. State how Seperate samples of the stereoisomers could be distinguished.
Optical isomerism. Equal volumes of each enantiomer, and so are optically inactive. Each enantiomer in a Separate sample will rotate plane polarised light in opposite directions.