Organic Chemistry IUPAC Naming

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44 Terms

1

Alkyne

carbon to carbon triple bond (class)

<p>carbon to carbon triple bond (class)</p>
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2

Amide

-CONH2, -CONH, -CONR2 (class)

<p>-CONH2, -CONH, -CONR2 (class)</p>
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3

Amine

-NH2 (Class)

<p>-NH2 (Class)</p>
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4

Phenyl

C6H5- (Functional Group)

<p>C6H5- (Functional Group)</p>
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5

Carboxylic acid

-COOH (Class)

<p>-COOH (Class)</p>
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6

Ester

-COOC/-COOR (Class)

<p>-COOC/-COOR (Class)</p>
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7

Alcohol

-OH (Class)

<p>-OH (Class)</p>
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8

Aldehyde

C=O (carbonyl at the end of the carbon chain) (Class)

<p>C=O (carbonyl at the end of the carbon chain) (Class)</p>
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9

Alkane

Hydrocarbon, all single bonds (Class)

<p>Hydrocarbon, all single bonds (Class)</p>
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10

Alkene

carbon to carbon double bond (Class)

<p>carbon to carbon double bond (Class)</p>
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11

Ether

-OR (alkoxy group) (Class)

<p>-OR (alkoxy group) (Class)</p>
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12

Ketone

-C=O (carbonyl group in the middle of a carbon chain) (Class)

<p>-C=O (carbonyl group in the middle of a carbon chain) (Class)</p>
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13

Halogenoalkane

-F

-Cl

-Br

-I (class)

<p>-F</p><p>-Cl</p><p>-Br</p><p>-I (class)</p>
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14

Hydroxyl

-OH (functional Group)

<p>-OH (functional Group)</p>
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15

-ol/anol

-OH (IUPAC suffix)

<p>-OH (IUPAC suffix)</p>
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16

alkenyl

C=C bond (Functional group)

<p>C=C bond (Functional group)</p>
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17

-ene

C=C (IUPAC suffix)

<p>C=C (IUPAC suffix)</p>
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18

Alkene (general formula)

CnH2n

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19

Alkane (general formula)

CnH2n+2

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20

Alkynyl

Carbon-to carbon triple bond (functional group)

<p>Carbon-to carbon triple bond (functional group)</p>
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21

Carbonyl (Aldehyde)

CHO (functional group)

<p>CHO (functional group)</p>
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22

Carbonyl (ketone)

RCOR`

<p>RCOR`</p>
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23

Carboxyl (acid)

COOH (functional group)

<p>COOH (functional group)</p>
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24

Carboxyl (Ester)

COOC, RCOOR (functional group)

<p>COOC, RCOOR (functional group)</p>
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25

Alkoxy

ROR` (functional group)

<p>ROR` (functional group)</p>
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26

Amido

CONH2 (functional group)

<p>CONH2 (functional group)</p>
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27

Amino

-NH2 (functional group)

<p>-NH2 (functional group)</p>
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28

-yne

Carbon-to-carbon triple bond (IUPAC suffix)

<p>Carbon-to-carbon triple bond (IUPAC suffix)</p>
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29

-oxyalkane

ROR (IUPAC suffix)

<p>ROR (IUPAC suffix)</p>
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30

-al, -anal

CHO (IUPAC suffix)

<p>CHO (IUPAC suffix)</p>
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31

-one, -anone

RCOR (IUPAC suffix)

<p>RCOR (IUPAC suffix)</p>
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32

-oic acid, anoic acid

COOH (IUPAC suffix)

<p>COOH (IUPAC suffix)</p>
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33

-anoate

COOC, RCOOR (IUPAC suffix)

<p>COOC, RCOOR (IUPAC suffix)</p>
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34

-anamide

CONH2 (IUPAC suffix)

<p>CONH2 (IUPAC suffix)</p>
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35

-anamiine

NH2 (IUPAC suffix)

<p>NH2 (IUPAC suffix)</p>
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36

amino-

NH2 (IUPAC prefix)

<p>NH2 (IUPAC prefix)</p>
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37

Halogeno-

Halogen (IUPAC prefix)

<p>Halogen (IUPAC prefix)</p>
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38

CnH2n+2O

Alcohol & ether (general formula)

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39

CnH2nO

Aldehyde & Ketone (general formula)

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40

CnH2nO2

Carboxylic acid & Ester (general formula)

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41

CnH2n-2

Alkyne (general formula)

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42

CnH2n+1NH2

Amine (general formula)

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43

CnH2n+1CONH2

Amide (general formula)

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44

CnH2n+1X

Halogenoalkane (general formula)

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