3.3.1 - Introduction to organic chemistry Flashcards

1
Q

Empirical formula definition

A

Simplest whole number ratio of atoms

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

Explain structural formula

A

Shows the arrangement of atoms in the molecule of a compound, without the bonds in between.

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

Displayed formula

A

Shows arrangments of all bonds and atoms

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

Homologous series have the same… (2)

A
  1. Functional group
  2. General formula
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Structural isomers have the same … but different …

A

The same molecular formula but different structural formula

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

2 types of stereoisomers

A
  1. Optical (enantiomers)
  2. Geometric (E-Z)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

3 types of structural isomers

A

Chain, positional, functional group (pent-1-ene vs cyclopentane)

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

Stereoisomers have the same … but different …

A

Same structural formula but different spatial arrangement of atoms.

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

Explain how the Cahn-Ingold-Prelog (CIP) priority rules can be used to deduce the full IUPAC name of this compound (6 marks)

A
  1. Consider atomic number of attached atoms
  2. X has higher atomic number than Y, takes prioity on RHS
  3. Both contain X atoms, move one bond away
  4. Z has a higher atomic number than W, takes priority
  5. Highest priority groups on the opposite/same side.
  6. Therefore it is E/Z
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Monochloro isomers

A

Isomers where the chlorine is placed in unique positions. (positional isomer)

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