Nomenclature Flashcards

1
Q

nomenclature of alkanes

A
  1. id longest chain​
    • use number prefix
    • use “-ane” suffix
  2. id substituents
  3. number carbons
    • substituents on lowest numbers possible
  4. group identical substituents together w/prefixes
  5. alphabetized substituents (ignore prefixes)

example = 4-isopropyl-2,3,3-trimethylheptane

(P 38-41)

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2
Q

nomenclature of haloalkanes

A
  • follow the same rule as simple alkanes
  • use halogen prefixes
    • F = fluoro-
    • Cl = chloro-
    • Br = bromo-
    • I = iodo-

(P 41-42)

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3
Q

nomenclature of alcohols

A
  • denote hydroxyl group with suffix to main alkyl chain (replace “e” with “-ol”)
  • place number of hydroxyl group after name of the longest C chain, before “-ol” suffix
    • give hydroxyl group the lowest number possible

example = 3-methylbutan-2-ol

(P 43-44)

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4
Q

1 carbon chain

A
  • prefix = meth-

(P 32)

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5
Q

2 carbon chain

A
  • prefix = eth-

(P 32)

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6
Q

3 carbon chain

A
  • prefix = prop-

(P 32)

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7
Q

4 carbon chain

A
  • prefix = but-

(P 32)

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8
Q

5 carbon chain

A
  • prefix = pent-

(P 32)

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9
Q

6 carbon chain

A
  • prefix = hex-

(P 32)

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10
Q

7 carbon chain

A
  • prefix = hept-

(P 32)

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11
Q

8 carbon chain

A
  • prefix = oct-

(P 32)

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12
Q

9 carbon chain

A
  • prefix = non-

(P 32)

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13
Q

10 carbon chain

A
  • prefix = dec-

(P 32)

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14
Q

methyl substituent

A
  • -CH3

(P 33)

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15
Q

ethyl substituent

A
  • -CH2CH3

(P 33)

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16
Q

propyl substituent

A
  • -CH2CH2CH3

(P 33)

17
Q

isopropyl substituent

A

(P 33)

18
Q

sec-butyl substituent

A

(P 33)

19
Q

tert-butyl

A

(P 33)

20
Q

alkane functional group

A
  • R3C-CR3

(P 34)

21
Q

alkene functional group

A
  • R2C=CR2

(P 34)

22
Q

alkyne functional group

A
  • RC ≡ CR

(P 34)

23
Q

alkyl halide functional group

A
  • R-X

(P 34)

24
Q

alcohol functional group

A
  • R-OH

(P 34)

25
Q

thiol functional group

A
  • R-SH

(P 34)

26
Q

ether functional group

A
  • R - O - R

(P 34)

27
Q

epoxide functional group

A

(P 34)

28
Q

phenol functional group

A