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Organic Chemistry
(the study of organic compounds, those
    containing the element carbon)

   QBA Miguel A. Castro Ramírez
CARBON

• Of the millions of known compounds in our
  world, 95% have a single element in
  common – CARBON.

• What is so special about carbon?
1. Our bodies are
made up of
organic comp’ds
We study organic compounds
because they are very important
to our lives.
• Most of the energy to run autos, trains and aircrafts, to
  heat our homes and offices, and to operate electrical
  equipment come from organic comp’ds.
• Organic compd’s in naturally occurring and synthetic
  medicines—aspirin, penicillin, anesthetics etc—relieve
  pain and illness.
• The active ingredients in soaps, detergents, polishes,
  cosmetics, deodorants, and shampoos are organic
  comp’ds.
• Materials for manufacturing artificial body parts, such as
  hip and knee prostheses, heart valves, and dentures, are
  organic comp’ds
• Synthetic plastics, textiles, and rubber are organic
  comp’ds. Our clothing are made from organic compd’s.
The Position of Carbon in the Periodic Table




   C lies at top of Grp 4A and is relatively small
element.
Carbon
•   Smallest member, and only nonmetal, of Group 4
•   Forms 4 covalent bonds
•   Forms single, double, and triple bonds
•   Bonds to itself, forming rings
“I am Carbon and I am Special”
     You can spend your whole life learning about me!

1.   I can form strong and short C-C bonds.


2.   I gladly form carbon-carbon double bonds (C=C), and I can
     even form carbon-carbon triple bonds (C≡C).


3.   I have no problem bonding to other elements (H, O, N, S,
     etc.–I love them all). Given where I am in the periodic table,
     I typically form four bonds, except in carbon monoxide (CO).
Some bonding possibilities for C
I Can Amaze You With Diversity
 Consider the number of compounds possible (23) from just 4
 single bonded C atoms, one O atom, the required H atoms


These are called structural isomers –compounds with the same
                                    chemical formulas, but different
                                    ways of connecting the atoms
                                     together to form different
                                     functional groups, or different
                                     compounds with completely
                                     different chemical and physical
                                     properties.
Two isomers of butane
       (C4H10)
n-butane
       Fig. 10.3a
iso-butane
   Fig. 10.3b
Molecular & Structural Formulas
• Molecular Formula - formula of the comp’d
 showing the number of atoms of each element in a
 molecule of the compound.
   Examples: CH3COOH, C2H4, etc.

• Structural Formula -- formula showing how
 various atoms in molecule are bonded together.
    Examples: See previous slide
Certain Parts of Me Make Me Behave in
       Certain Predictable Ways

Functional Groups – atoms or specific groups of atoms in
                 a molecule that impart specific chemical
                and physical properties to the molecule.

          The secret to learning organic chemistry.



As the periodic table is to inorganic chemistry, functional
groups are the easy way to learn organic chemistry.
Four of the Functional Groups

Alcohol group - Hydroxyl group     Ether group

          ..                                    ..
     C
          ..
          O     H
                                       C        O        C
                                                ..
      Alcohol
                                           Ether

   Carboxylic acid group          Ester group
         ..                       ..
         O                        O
         ..




               ..                ..        ..
         C
               ..
               O    H             C
                                           ..
                                           O         C
       Carboxyl                        Ester
Structures & Classes of
 Hydrocarbons (HCs)
There are four families of hydrocarbons:
alkanes, alkenes, alkynes, and aromatics.
Saturation
• Alkanes are saturated; they contain the maximum
  number of hydrogen atoms per carbon atom.

• Alkenes and alkynes are unsaturated. They
  contain at least one double or triple bond,
  respectively. They have fewer hydrogen atoms
  per carbon atom than alkanes.
Hydrocarbons (HCs)                           C + H

Saturated hydrocarbons
Alkanes: general formula is CnH2n+2 (all C-C bonds)
Cycloalkanes: general formula is CnH2n
(n is a positive whole number for all HCs)

Unsaturated hydrocarbons
Alkenes: general formula is CnH2n (C=C bonds)
Alkynes: general formula is CnH2n–2 (C≡C bonds)
Aromatics: usually contain one or more rings of six C
atoms called benzene rings
(n is a positive whole number for all HCs)
Naming

• Straight chain alkanes
  are named with a base
  name depending on
  the number of atoms
  in the carbon chain
  and the suffix –ane.
The most important property of the alkanes is
 their flammability, the combustion reaction
  between oxygen and the alkane producing
          carbon dioxide and water.
More on Functional
     Groups
Functionalized Hydrocarbons
• Basic hydrocarbon structures form a foundation for a
  major grouping of organic compounds.
• Contain additional atoms or groups of atoms
• Insertion of functional groups to a hydrocarbon
  dramatically alters its properties.
Representing Functionality
Compounds containing the same functional
 group are called a family.
Generic symbolism is R-FG where R is the
 hydrocarbon part of the molecule and FG is
 the functional group.
           R-OH symbolizes the alcohols.
Functional groups help organize and classify
  organic compounds.
Chlorinated Hydrocarbons
• Found in pesticides, solvents, refrigerant liquids
• One or more chlorine atoms substitute for one or
  more hydrogen atoms
• Lower flammability and reactivity than hydrocarbons
CFCs

• Chlorofluorocarbons are a subfamily of
  chlorinated hydrocarbons.
• Chemically stable . . .
• Until they reach the high-energy sunlight in
  the upper atmosphere
• Ozone destruction led to bans.
Alcohols
• General formula: R-OH
• Additional of the –OH makes alcohols
  polar.
• Increased intermolecular attractive forces
  makes alcohols liquids.
• Naming involves modifying the
  hydrocarbon name with an ending of –ol.
Ethanol
• Alcoholic beverages
• Gasoline additive
• Sugar fermentation



• CNS depressant
• Adverse health effects
Other Alcohols
• Isopropyl alcohol is
  commonly known as
                         • Methanol is toxic to
  rubbing alcohol.
                           the human liver.
                         • Ethanol is
                           administered as an
                           antidote.
Aldehydes and Ketones
• Commonly found in pleasant flavors and aromas
• Contain the carbonyl group: Carbon double
  bonded to an oxygen atom
Formulas
• Aldehydes
  – General formula:
    RCHO, includes
    carbonyl group
  – Named according to
    length carbon chain
    with the ending of –al
    or –aldehyde             • Preservation of
  – Methanal or
                               biological specimens
    formaldehyde
Formulas
• Ketones
  – Similar to aldehydes
    but have two R groups
    with the carbonyl
  – Names end in –one
  – Acetone is the simplest
    ketone.

                              • Nail polish removal
Carboxylic Acids
• Commonly found in sour foods
• General formula: RCOOH
• One of these oxygen atoms is bonded as a
  carbonyl group, as in aldehydes and
  ketones.
Esters
• Esters have pleasant odors.
• General formula: RCOOR
• Named according to the relevant R
  groups and ending with –ate
Ethers
• Ethers contain the functional group –O-
• General formula: ROR
• Named according to the two R groups
  and given the ending ether




                                • Formerly used as an
                                  anesthetic
Amines
• Amines are organic compounds that
  contain nitrogen.
• General formula: NR3
• Notable for disagreeable odors
• Named for R groups present and
  ending in –amine

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ORGANIC CHEMISTRY

  • 1. Organic Chemistry (the study of organic compounds, those containing the element carbon) QBA Miguel A. Castro Ramírez
  • 2. CARBON • Of the millions of known compounds in our world, 95% have a single element in common – CARBON. • What is so special about carbon?
  • 3. 1. Our bodies are made up of organic comp’ds
  • 4. We study organic compounds because they are very important to our lives.
  • 5. • Most of the energy to run autos, trains and aircrafts, to heat our homes and offices, and to operate electrical equipment come from organic comp’ds. • Organic compd’s in naturally occurring and synthetic medicines—aspirin, penicillin, anesthetics etc—relieve pain and illness. • The active ingredients in soaps, detergents, polishes, cosmetics, deodorants, and shampoos are organic comp’ds. • Materials for manufacturing artificial body parts, such as hip and knee prostheses, heart valves, and dentures, are organic comp’ds • Synthetic plastics, textiles, and rubber are organic comp’ds. Our clothing are made from organic compd’s.
  • 6. The Position of Carbon in the Periodic Table C lies at top of Grp 4A and is relatively small element.
  • 7. Carbon • Smallest member, and only nonmetal, of Group 4 • Forms 4 covalent bonds • Forms single, double, and triple bonds • Bonds to itself, forming rings
  • 8. “I am Carbon and I am Special” You can spend your whole life learning about me! 1. I can form strong and short C-C bonds. 2. I gladly form carbon-carbon double bonds (C=C), and I can even form carbon-carbon triple bonds (C≡C). 3. I have no problem bonding to other elements (H, O, N, S, etc.–I love them all). Given where I am in the periodic table, I typically form four bonds, except in carbon monoxide (CO).
  • 10. I Can Amaze You With Diversity Consider the number of compounds possible (23) from just 4 single bonded C atoms, one O atom, the required H atoms These are called structural isomers –compounds with the same chemical formulas, but different ways of connecting the atoms together to form different functional groups, or different compounds with completely different chemical and physical properties.
  • 11.
  • 12. Two isomers of butane (C4H10)
  • 13. n-butane Fig. 10.3a
  • 14. iso-butane Fig. 10.3b
  • 15. Molecular & Structural Formulas • Molecular Formula - formula of the comp’d showing the number of atoms of each element in a molecule of the compound. Examples: CH3COOH, C2H4, etc. • Structural Formula -- formula showing how various atoms in molecule are bonded together. Examples: See previous slide
  • 16. Certain Parts of Me Make Me Behave in Certain Predictable Ways Functional Groups – atoms or specific groups of atoms in a molecule that impart specific chemical and physical properties to the molecule. The secret to learning organic chemistry. As the periodic table is to inorganic chemistry, functional groups are the easy way to learn organic chemistry.
  • 17.
  • 18.
  • 19. Four of the Functional Groups Alcohol group - Hydroxyl group Ether group .. .. C .. O H C O C .. Alcohol Ether Carboxylic acid group Ester group .. .. O O .. .. .. .. C .. O H C .. O C Carboxyl Ester
  • 20.
  • 21.
  • 22. Structures & Classes of Hydrocarbons (HCs)
  • 23. There are four families of hydrocarbons: alkanes, alkenes, alkynes, and aromatics.
  • 24. Saturation • Alkanes are saturated; they contain the maximum number of hydrogen atoms per carbon atom. • Alkenes and alkynes are unsaturated. They contain at least one double or triple bond, respectively. They have fewer hydrogen atoms per carbon atom than alkanes.
  • 25. Hydrocarbons (HCs) C + H Saturated hydrocarbons Alkanes: general formula is CnH2n+2 (all C-C bonds) Cycloalkanes: general formula is CnH2n (n is a positive whole number for all HCs) Unsaturated hydrocarbons Alkenes: general formula is CnH2n (C=C bonds) Alkynes: general formula is CnH2n–2 (C≡C bonds) Aromatics: usually contain one or more rings of six C atoms called benzene rings (n is a positive whole number for all HCs)
  • 26.
  • 27.
  • 28. Naming • Straight chain alkanes are named with a base name depending on the number of atoms in the carbon chain and the suffix –ane.
  • 29.
  • 30. The most important property of the alkanes is their flammability, the combustion reaction between oxygen and the alkane producing carbon dioxide and water.
  • 32. Functionalized Hydrocarbons • Basic hydrocarbon structures form a foundation for a major grouping of organic compounds. • Contain additional atoms or groups of atoms • Insertion of functional groups to a hydrocarbon dramatically alters its properties.
  • 33. Representing Functionality Compounds containing the same functional group are called a family. Generic symbolism is R-FG where R is the hydrocarbon part of the molecule and FG is the functional group. R-OH symbolizes the alcohols. Functional groups help organize and classify organic compounds.
  • 34. Chlorinated Hydrocarbons • Found in pesticides, solvents, refrigerant liquids • One or more chlorine atoms substitute for one or more hydrogen atoms • Lower flammability and reactivity than hydrocarbons
  • 35. CFCs • Chlorofluorocarbons are a subfamily of chlorinated hydrocarbons. • Chemically stable . . . • Until they reach the high-energy sunlight in the upper atmosphere • Ozone destruction led to bans.
  • 36.
  • 37. Alcohols • General formula: R-OH • Additional of the –OH makes alcohols polar. • Increased intermolecular attractive forces makes alcohols liquids. • Naming involves modifying the hydrocarbon name with an ending of –ol.
  • 38. Ethanol • Alcoholic beverages • Gasoline additive • Sugar fermentation • CNS depressant • Adverse health effects
  • 39. Other Alcohols • Isopropyl alcohol is commonly known as • Methanol is toxic to rubbing alcohol. the human liver. • Ethanol is administered as an antidote.
  • 40. Aldehydes and Ketones • Commonly found in pleasant flavors and aromas • Contain the carbonyl group: Carbon double bonded to an oxygen atom
  • 41. Formulas • Aldehydes – General formula: RCHO, includes carbonyl group – Named according to length carbon chain with the ending of –al or –aldehyde • Preservation of – Methanal or biological specimens formaldehyde
  • 42. Formulas • Ketones – Similar to aldehydes but have two R groups with the carbonyl – Names end in –one – Acetone is the simplest ketone. • Nail polish removal
  • 43. Carboxylic Acids • Commonly found in sour foods • General formula: RCOOH • One of these oxygen atoms is bonded as a carbonyl group, as in aldehydes and ketones.
  • 44.
  • 45. Esters • Esters have pleasant odors. • General formula: RCOOR • Named according to the relevant R groups and ending with –ate
  • 46. Ethers • Ethers contain the functional group –O- • General formula: ROR • Named according to the two R groups and given the ending ether • Formerly used as an anesthetic
  • 47. Amines • Amines are organic compounds that contain nitrogen. • General formula: NR3 • Notable for disagreeable odors • Named for R groups present and ending in –amine