Introduction to Organic Chemistry Flashcards

(29 cards)

1
Q

How does Carbon bond?

A
  • Has 4 electrons in its outer shell
  • Can form 4 single bonds
  • Can form 2 double bonds
  • Can form 1 triple bond and 1 single bond
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Functional Group

A

Responsible for the different chemical and physical properties of the compound

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

Homologous Series

A

A group of compounds with the same functional group that differ by a CH2

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

How can you represent organic compounds?

A
  • Empirical Formula
  • Molecular Formula
  • Displayed Formula
  • Structural Formula
  • Skeletal Formula
  • 3D (Shape of Molecules)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Empirical Formula

A
  • Simplest ratio of the atoms of each element in a compound
  • Calculate by dividing the mass (or percentage given) by the atomic mass of each element to find the moles
  • Then divide the number of moles of each element by the smallest number calculated
  • Multiply out to get whole numbers if one comes out as a decimal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Molecular Formula

A
  • The actual number of atoms of each element in a molecule
  • Calculate the Mr of the empirical formula
  • Divide the Mr of the molecular formula by the Mr of the empirical formula
  • Multiply each atom in the empirical formula by the answer to step 2
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Displayed Formula

A

Shows all the atoms and bonds in the molecule (single bonds, double bonds, triple bonds, etc)

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

Structural Formula

A

Shows the unique arrangement of atoms in a molecule in simplified form, without showing all the bonds

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

Skeletal Formula

A
  • Uses lines to show the bonds but don’t draw the carbons at all
  • The ends of the lines are carbon atoms (unless specified otherwise)
  • It is assumed there are the correct number fof hydrogen atoms on the carbons
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

3D Structures

A
  • Show how the model looks in 3D
  • Use a dashed line to show the atoms going away from us
  • Use a wedged line to show the atoms coming towards us
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What system is used to name Organic Compounds?

A

IUPAC Systematic Naming Method

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

What does the root of the name show?

A

What the longest unbranched hydrocarbon is

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

What do suffixes show?

A

Functional Group

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

What do prefixes show?

A

Side chains or haloalkenes

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

Why do we number the longest chain?

A

The numbers for prefixes and suffixes show which number carbon the prefix or suffix is on in the longest chain

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

Isomers

A

Molecules that have the same molecular formula but different atom arrangements

17
Q

2 Types of isomerism

A
  • Structural isomerism
  • Stereoisomerism
18
Q

Types of Structural Isomerism

A
  • Position Isomerism
  • Functional Group Isomerism
  • Chain Isomerism
19
Q

Types of Stereoisomerism

A
  • Geometric/E-Z Isomerism
  • Optical Isomerism
20
Q

Structural Isomers

A

Same molecular formula but different structural formula

21
Q

Position Isomers

A
  • Same functional group but at different carbons on the chain
  • E.g Propan-1-ol and propan-2-ol
22
Q

Functional Group Isomers

A
  • Different functional groups
  • E.g. Ethanol and methoxymethane (an ether)
23
Q

Stereoisomerism

A

When 2 or more compounds have the same structural formula but different arrangements of atoms in space

24
Q

E-Z (Geometric) Isomerism

A

Restricted rotation around the double bond

25
Z Isomers
The isomer with the priority groups on the same side of the double bond (AKA Cis)
26
E Isomers
The isomer with the priority groups on opposite sides (AKA Trans)
27
How can you identify priority groups?
The atom or compound that has the higher atomic number is the priority group
28
When is there no E-Z isomerism?
- When either carbon of the double bond has 2 of the exact same group on it - When there is no double bond
29