1 O O 5. Organic Acids 6. Esters Carboxyl group - - PDF document

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1 O O 5. Organic Acids 6. Esters Carboxyl group - - PDF document

Functional Groups: something that replace a H in a hydrocarbon H H H X Topic 12.1 C C C H H H H O 1. Alcohol Hydroxyl group (-OH) replacing a H 2. Aldehyde Carbonyl group at end of chain -CH H H OH H OH H H H H H


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SLIDE 1

1

Topic 12.1 Functional Groups:

something that replace a H in a hydrocarbon C C

X

H H H H H C H H C C

OH

H H H H H C H H C C H H H H OH C H H H C C CH3 H H H OH C H H H Primary Secondary Tertiary

  • 1. Alcohol

Hydroxyl group (-OH) replacing a H Propanol 2-Propanol 2-methyl-2-Propanol

R-OH

General formula: 3 classes :

  • Not bases
  • Do not dissociate
  • Not electrolytes
  • 2. Aldehyde

Propanal

General formula: Carbonyl group at end of chain

C C H H H H H H C O

  • CH

O

R-CH O

  • Not electrolytes
  • 3. Ketone

Propanone

General formula: Carbonyl group inside chain

  • C-

O

2-pentanone

C C H H H H H H C O

  • Not electrolytes

H C H H C C H H H H H C O C H H

  • 4. Ether

Ethylmethyl ether General formula:

R-O-R’

Oxygen Connecting two hydrocarbon chains C C H H H H H H O C H H

  • Not electrolytes
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SLIDE 2

2

  • 5. Organic Acids

Propanoic Acid

General formula: Carboxyl group of chain

  • C-OH

O Acidic hydrogen (H+)

R-C-OH O

C C OH H H H H H C O

  • Weak acids
  • Do dissociate
  • weak electrolytes
  • 6. Esters

Butyl

General formula: Carboxyl group in middle of chain

  • C-O

O Comes from acid Comes from alcohol

Propanoate

R-C-O-R’ O

C C O H H H H H C O C H H C H H C H H C H H H

  • Not electrolytes
  • 7. Amines

General formula: R-NH2 = organic compounds based on ammonia

Methylamine Methanamine

N CH2 C H2 C H2 C H3 CH3 CH3

Triethylamine Triethanamine

N H H H

:

N H H C : H H H

  • weak bases
  • Split water
  • weak electrolytes
  • 8. Amino acids = have an amino and a carboxyl group

C OH O N H H C R H

O O C H2 C H2 C H2 C H2 CH3 C H2 C H3

C H3 C H2 C H2 C H2 C H2 OH

O C H2 C H2 C H2 C H2 C H3 CH3 CH O C H2 C H2 C H2 C H3 O C H3 C H2 C H2 C H2 C H2 CH3 C H3 C H2 C H C H2 C H2 C H2 CH3 OH

Structure general formula type of compound name

1 2 3 4 5 6 R-OH R-OH R-CH O R-O-R’ ester aldehyde ketone ether 2° alcohol 1° alcohol R-C-O-R’ O propylpentanoate pentanal 3-heptanone butyl ethyl ether 3-heptanol 1-pentanol

OH O C H3 C H2 C H2 C H2 C H2 C H2 O O C H2 C H2 C H2 C H2 CH3 C H3 OH C H2 C H2 C H2 C H2 C H3 CH3 CH3 CH O C H2 C H2 C H2 C H C H3 CH3 O C H3 C H2 C H2 CH3 O C H2 C H2 CH3 C H2 C H2 C H2 C H2 C H3

Structure general formula type of compound name

7 8 9 10 11 12 R-OH R-CH O R-O-R’

  • rg. acid

aldehyde 3° alcohol ketone ether ester R-C-O-H O heptanoic acid 5-methyl hexanal 2-methyl 2-heptanol 2-pentanone propyl pentyl ether ethyl pentanoate R-C-O-R’ O

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SLIDE 3

3

OH O C H3 C H2 C H2 C H2 C H2 C H2 C H2 OH CH3 C H2 C H2 CH3 C H2 C H3

Structure general formula type of compound name

11 12

  • rg. acid

3° alcohol hexanoic acid 4-methyl 4-octanol R-OH R-C-OH O