Organic Chemistry Naming Flashcards

1
Q

Alkane

A
  1. Contains hydrogen and carbon
  2. Single bonds between carbon atoms
  3. General formula: CnH2n+2
  4. Suffix: ane

Example :
C3H8- propane

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2
Q

Alkene

A
  1. Contains hydrogen and carbon
  2. At least one double bond between carbon atoms
  3. General formula: CnH2n
  4. Suffix: ene

Example :
prop-1-ene - C3H6

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3
Q

alkyne

A
  1. Contains hydrogen and carbon
  2. At least one triple bond between carbon atoms
  3. General formula: CnH2n-1
  4. Suffix: yne

Example :
prop-1-yne

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4
Q

Alcohol

A
  1. Contains a hydroxyl functional group (-OH)
  2. Always number from end closest to functional group
  3. General formula: CnH2n+2O
  4. Suffix: ol

Example :
Butan-2-ol C4H10O

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5
Q

Aldehyde

A
  1. Contains a carbon (C=O) on terminal carbon
  2. As C=O is always at the end of the parent chain and we number the end closest to functional group C=O is always 1 - do not need to specify in name
  3. General formula: CnH2nO
  4. Suffix: al

Example :
propanal C3H6O

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6
Q

Ketone

A
  1. Contains a carbonyl group (C=O) not on terminal carbon
  2. C=O functional group needs location
  3. General formula: CnH2nO
  4. Suffix: one

Example :
pentan-3-one C5H10O

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7
Q

Carboxylic acid

A
  1. Contains a carboxyl functional group
  2. Carboxyl is always at the end of the parent chain - don’t need to specify location
  3. General formula: CnH2nO2
  4. Suffix: oic acid

Example :
Butanoic acid C4H8O2

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8
Q

Haloalkanes

A
  1. Contains at least one halogen (group 17) off a carbon
  2. Number the chain so halogen is attached to lowest carbon group
  3. Halogen stems end in “O” and placed before alkane with location

Example :
2-chloropropane
2-chloro-2-idobutane
2,2-dibromo-3chloropentane
2-chloro-3,4-diflurohexane

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9
Q

branched molecules

A
  • also called side chains
  • branches end in “yl”

e.g. Methyl
2,3 -dimethyl butane

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10
Q

Cyclic molecules

A
  • a cyclic hydrocarbon has a ring of carbons and cyclo as a prefix
  • ring is the main chain if it has the most carbons otherwise it is a cylcoalkyl group
    -if there is only one branch or double/triple bond is number 1
  • if multiple branches, number carbons to give lowest combination of numbers

E.g.
Cyclobutane
2-ethyl -3,3-dimethylcyclohex-ene

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11
Q

Amine

A

NH2
- contain carbon, hydrogen, and nitrogen atoms
- contains an amino functional group
- number from end closest to functional group
- suffix: amine (drop e off alkane)

E.g.
propan-1-amine

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12
Q

Nitriles

A

C triple bond N
- contain carbon, hydrogen, and nitrogen atoms
- contains an amino functional group
- nitrile carbon will be carbon 1 (don’t need to specify in name)
- suffix: nitrile

E.g. Propane nitrile

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13
Q

Esters

A
  • contains carbon, hydrogen and oxygen atoms
  • contains an ester functional group
  • form from the reaction of carboxylic acid and an alcohol
  • first word - from the alcohol part and ends in “yl”
    second word - from the carboxylic acid part and ends in “oate”

E.g.
Propyl ethanoate

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14
Q

Amides

A
  • contain carbon, hydrogen, oxygen and nitrogen atoms
  • contains an amide functional group
  • similar to carboxylic acid but -OH is an -NH2
  • Main chain will have carbonyl group and this carbon will renumber one
  • suffix: amide

E.g.
propanamide
N-methyl butanamide

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15
Q

Poly functional compounds

A
  • more than one functional group
    –> if the functional group is the same use a multiplier prefix
    –> if functional groups are different, need to look at priorities
  • functional group with highest priority is assigned lowest number and suffix used
  • lower priority functional groups indicated by a prefix

Highest priority
- carboxyl

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