L1 Functional groups Flashcards

(38 cards)

1
Q
A

Name: Alkene (double bond)
Name ending: -ene
Example: H2C=CH2 ethene

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2
Q
A

Name: Alkyne (triple bond)
Name ending: -yne
Example:

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3
Q
A

Name: Arene (aromatic ring)
Name ending: none
Example:

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4
Q
A

Name: Halide
Name ending: None
Example: CH3Cl - chloromethane

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5
Q
A

Name: Alcohol
Name ending: -ol
Example: CH3OH - methanol

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6
Q
A

Name: Ether
Name ending: ether
Example: CH3OCH3 - dimethyl ether

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7
Q
A

Name: Monophosphate
Name ending: phosphate
Example: CH3OPO32- - methyl phosphate

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8
Q
A

Name: Diphosphate
Name ending: diphosphate
Example: CH3OP2O63- - methyl diphosphate

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9
Q
A

Name: Amine
Name ending: -amine
Example: CH3NH2 - methylamine

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10
Q
A

Name: Imine (Schiff base)
Name ending: none
Example:

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11
Q
A

Name: Nitrile
Name ending: -nitrile
Example:

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12
Q
A

Name: Thiol
Name ending: -thiol
Example: CH3SH - methanethiol

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13
Q
A

Name: Sulfide
Name ending: sulfide
Example: CH3SCH3 - dimethyl sulfide

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14
Q
A

Name: Disulfide
Name ending: disulfide
Example: CH3SSCH3 - dimethyl disulfide

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15
Q
A

Name: Sulfoxide
Name ending: sulfoxide
Example:

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16
Q
A

Name: Aldehyde
Name ending: -al
Example:

17
Q
A

Name: Ketone
Name ending: -one
Example:

18
Q
A

Name: Carboxylic acid
Name ending: -oic acid
Example:

19
Q
A

Name: Ester
Name ending: -oate
Example:

20
Q
A

Name: Thioester
Name ending: -thioate
Example:

21
Q
A

Name: Amide
Name ending: -amide
Example:

22
Q
A

Name: Acid chloride
Name ending: -oyl chloride
Example:

23
Q
A

Name: Carboxylic acid anhydride
Name ending: -oic anhydride
Example:

24
Q

alkanes

A
  • simplest family of hydrocarbons
  • CnH2n+2
25
Methane
CH4
26
Ethane
C2H6
27
Propane
C3H8
28
Butane
C4H10
29
Pentane
C5H12
30
Hexane
C6H14
31
Heptane
C7H16
32
Octane
C8H18
33
Nonane
C9H20
34
Decane
C10H22
35
alkyl group -
alkane molecule missing one H
36
primary, sec, tert, and quarternary carbons:
depending on how many other carbons are attached to the **branching carbon**
37
**R** in organic chemistry:
*generalized* organic group, **R**est of the molecule
38
b-mercaptoethanol (BME) usage:
can be used to reduce disulfide bonds & can act as a biological antioxidant