3.3.1 Nomenclature Flashcards

1
Q

Types of Formula - Displayed

A

Shows all atoms and all covalent bonds

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2
Q

Types of Formula - Empirical

A

The simplest whole number ratio of atoms in a compound

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3
Q

Types of Formula - Molecular (2)

A

Actual numbers of atoms in a compound

No indication of arrangement

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4
Q

Types of Formula - Skeletal (2)

A

Shortened diagram showing only the carbon chain and functional groups attached to it (no hydrogen bonds shown)
Each point represents one carbon

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5
Q

Types of Formula - Structural

A

Follows a carbon by carbon approach

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6
Q

Types of Formula - General

A

Relates to a homologous series

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7
Q

Prefixes - Two

A

Di-

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8
Q

Prefixes - Three

A

Tri-

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9
Q

Prefixes - Four

A

Tetra-

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10
Q

Prefixes - Five

A

Penta-

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11
Q

Prefixes - Six

A

Hexa-

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12
Q

Prefixes - Chlorine

A

Chloro-

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13
Q

Prefixes - Bromine

A

Bromo-

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14
Q

Prefixes - Fluorine

A

Fluoro-

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15
Q

Prefixes - Iodine

A

Iodo-

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16
Q

Alkyls - 1 carbon

A

Methyl

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17
Q

Alkyls - 2 carbons

A

Ethyl

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18
Q

Alkyls - 3 carbons

A

Propyl

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19
Q

Alkyls - 4 carbons

A

Butyl

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20
Q

Alkyls - 5 carbons

A

Pentyl

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21
Q

Alkyls - 6 carbons

A

Hexyl

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22
Q

Alkyls - 7 carbons

A

Heptyl

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23
Q

Alkyls - 8 carbons

24
Q

Alkyls - 9 carbons

25
Alkyls - 10 carbons
Decyl
26
Prefixes - 1 carbon
Meth-
27
Prefixes - 2 carbons
Eth-
28
Prefixes - 3 carbons
Prop-
29
Prefixes - 4 carbons
But-
30
Prefixes - 5 carbons
Pent-
31
Prefixes - 6 carbons
Hex-
32
Prefixes - 7 carbons
Hept-
33
Prefixes - 8 carbons
Oct-
34
Prefixes - 9 carbons
Non-
35
Prefixes - 10 carbons
Dec-
36
Prefixes - Cyclic compounds
Cyclo-
37
Types of chain (3)
Straight chain Cyclic compound Branched chain
38
How are compounds named? (5)
Find the longest consecutive carbon chain Find functional groups and add prefix if there are multiple of the same Number the chain so lowest numbers are used / highest priority functional group has lowest number Order the alkyl groups in alphabetical order (excluding prefixes) Use commas to separate numbers and hyphens to separate letters and numbers
39
Priority Functional Groups - Carboxylic acid
Priority: 1 Suffix: -oic acid Prefix: N/A Functional group: carbon, double bond O, single bond OH
40
Priority Functional Groups - Ester
Priority: 2 Suffix: -oate Prefix: N/A Functional group: carbon, double bond oxygen, single bond oxygen
41
Priority Functional Groups - Acyl chloride
Priority: 3 Suffix: -oyl chloride Prefix: N/A Functional group: carbon, double bond oxygen, single bond chlorine
42
Priority Functional Groups - Nitrile
Priority: 4 Suffix: -nitrile Prefix: N/A Functional group: carbon, triple bond nitrogen
43
Priority Functional Groups - Aldehyde
Priority: 5 Suffix: -al Prefix: N/A Functional group: carbon, double bond oxygen, single bond hydrogen
44
Priority Functional Groups - Ketone
Priority: 6 Suffix: -one Prefix: oxo- Functional group: carbon, double bond oxygen
45
Priority Functional Groups - Alcohol
Priority: 7 Suffix: -ol Prefix: hydroxy- Functional group: single bond OH
46
Priority Functional Groups - Amine
Priority: 8 Suffix: -amine Prefix: amino- Functional group: single bond NH2
47
Priority Functional Groups - Alkene
Priority: 9 Suffix: -ene Prefix: N/A Functional group: double bond carbon
48
Priority Functional Groups - Halogenoalkene
Priority: 10 Suffix: -ene Prefix: e.g. chloro- bromo- iodo-
49
What is an isomer?
A compound with the same molecular formula but arranged differently
50
Structural Isomers - Chain
Same functional group, different carbon skeleton
51
Structural Isomers - Position
Same skeleton, different position on carbon chain
52
Structural Isomers - Functional Group
Same atoms, different functional groups
53
What is a stereoisomer?
Same formula but different arrangement of atoms in space
54
What is E/Z isomerism? (3)
The restricted rotation around the C=C bond in alkenes means atoms can be in a different orientation in space Z - same side E - different side
55
How are E/Z Isomers names according to the Cahn-Ingold-Prelog priority rules? (3)
The chains attached to the double bond are assigned priority based off of the highest atomic number If the two highest priority groups are both above or both below the double bond, the molecule is a Z isomer If the highest priority groups are diagonally across from each other, the molecule is an E isomer
56
Why do Z Isomers have a higher melting/boiling point than E Isomers? (2)
They can pack closer together | This strengthens the Van der Waals forces