Intro Flashcards

1
Q

What is organic chemistry?

A

The Chemistry of carbon containing compounds

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

Why does carbon form vast numbers of compounds?

A

It can form strong covalent bonds with itself

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

What do the physical and chemical properties of organic compounds depend on?

A

The number and arrangement of carbon atoms in the molecule

The functional group of the compound

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

What is a functional group?

A

A specific atom/group of atoms which give certain physical and chemical properties to the molecule

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

Define homologous series

A

Organic compounds with the same functional group but different number of C atoms

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

Give the 4 main characteristics of a homologous series

A

Same general formula

Similar chemical properties

Trend in physical properties

One differs from the next by CH2

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

Give the general formula of alkanes

A

Cn H2n+2

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

Give the general formula of cycloalkanes

A

Cn C2n

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

Give the general formula of alkenes

A

Cn H2n

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

Give the functional group of Haloalkanes

A

|
-C-halogen
|

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

Give the suffix for alkanes

A

-ane

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

Give the prefix/ suffix for cycloalkanes

A

Cyclo…ane

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

Give the prefix/ suffix for alkenes

What is the functional group

A

-ene

C=C

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

Give the prefix/ suffix for haloalkanes

A
Fluoro- 
Chloro 
Bromo-
Iodo-  
                    -ane
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Give the prefix/ suffix for alcohols

What is the functional group

A

___ ol

OR

hydroxy_____

-OH

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

Give the prefix/ suffix for aldehydes

Give the functional group

A

___al

-C=O
|
H

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Give the prefix/ suffix for ketones

What is the functional group

A

_____one

 C
 |
C=O
 |
C
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Give the prefix/ suffix for carboxylic acids

Give the functional group

A

___oic acid

-C=O
|
OH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Give the prefix/ suffix for acyl chlorides

Give the functional group

A

___oyl chloride

O
|| R-C-Cl
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Give the prefix/ suffix for acid anhydrides

A

-anoic anhydride

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Give the prefix/ suffix for esters

Give functional group

A

-yl ___anoate

O 
|| R-C-OR’
22
Q

Give the prefix/ suffix for nitriles

Give the functional group

A

-ane nitrile

N
|||
C-

23
Q

Give the prefix/ suffix for amines

Give the functional group

A

___yl amine

OR

Amino____ ane

|
C-NH2
|

24
Q

Give the prefix/ suffix for amides

Give the functional group

A

-amide

O
|| R-C-NH2
25
Give the prefix/ suffix for N-substituted amides
N- ___ yl -anamide Eg N-methyl ethanamide
26
Give the functional group for N substituted amides
``` O || R-C-N-R’ | H ```
27
Give the prefix/ suffix for aromatics
Phenyl____ OR - benzene
28
Give the functional group for acid anhydrides
O O || || R-C-O-C-R
29
Define molecule formula
Shows the actual number of atoms of each element in a compound
30
Define empirical formula
The simplest whole number ratio of atoms of each element in a compound
31
Define structural formula
Show how the atoms are joined together in a molecule
32
Define displayed formula
Shows every atom and every bond in a molecule
33
Define skeletal formula
Uses lines to represent bonds Each point represents a C atom H atoms and bonds to them are not usually shown unless part of a functional group
34
How to remember order of methyl, ethyl etc
Monkeys Eat Peanut Butter
35
What order are prefixes put into? Are di, tri, tetra, etc taken into account
Alphabetical No
36
If more than one of the same functional group is present what do you use for nomenclature
``` 2- di 3- tri 4- tetra 5- penta 6- hexa ```
37
Define structural isomerism
Same molecular formula but different structural formula
38
Define stereoisomerism
Same structural formula but a different arrangement in space
39
3 kinds of structural isomerism
Chain Position Functional group
40
2 types of stereoisomers
Geometric | Optical
41
Define chain isomerism
Same molecular formula but different length Carbon chain
42
Define position isomer
Same molecular formula and same length C chain but functional group is attached at different positions along the chain
43
Define functional group isomerism
Same molecular formula but different functional group
44
# Define a) general formula b) Molecular formula | c) empirical formula
Shows the number of atoms of each element in a substance with n carbon atoms Shows the actual number of atoms of each element Simplest whole number ratio of atoms of each element
45
# Define structural formula Define displayed formula
Shows how the atoms are joined together in a molecule Shows every atom and every bone in the molecule
46
What does IUPAC stand for
International Union for Pure and Applied Chemistry
47
What are priority rules for E Z
Stage 1: consider atomic number of atoms on left side carbon of C=C High atomic number takes priority If both atoms the same consider atoms 1 bond further away. Atom with higher atomic number takes priority Stage 2: repeat for RHS Stage 3: if Priority on the same side =Z of on opposite = E
48
How are stereoisomers used in biology?
Enzymes catalysed reactions result in stereospecific products eg (+) glucose can be digested but (-) glucose cannot One enantiomer of aspartic acid tastes sweet whereas the other tastes bitter DRUGS - (lock and key model)
49
How would you overcome the problem of a racemic mixture for drugs?
Separate isomers which is difficult because they have the same chemical properties Sell the drug as a mixture (but half is useless) Only make the required isomer
50
What was the problem for thalidomide?
The body could convert the useful enantiomer into the dangerous one naturally