1 / 42

Chapter 2. Fundamental Concepts in Understanding Bioenergy and Biobased Products

Chapter 2. Fundamental Concepts in Understanding Bioenergy and Biobased Products. Organic Chemistry. What is Organic Chemistry???. The original distinction between inorganic and organic compounds was their source in nature: Inorganic Compounds => Mineral Sources

alaric
Download Presentation

Chapter 2. Fundamental Concepts in Understanding Bioenergy and Biobased Products

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 2. Fundamental Concepts in Understanding Bioenergy and Biobased Products Organic Chemistry

  2. What is Organic Chemistry??? • The original distinction between inorganic and organic compounds was their source in nature: • Inorganic Compounds => Mineral Sources • Organic Compounds => Plants and Animals • However, the most of organic compounds are now produced from petroleum. • The common feature of organic compounds isa skeleton of carbon that is surrounded by other atoms, especially hydrogen, oxygen and nitrogen, but also sulfur, phosphorus, and halides.

  3. A Variety of Reactions Among Organic Compounds • Addition: (e.g.) A + B  A-B • Elimination: (e.g.) A-B  A + B • Substitution: Replacement of one atom or the group of atoms by a second atom or group of atoms • (e.g.) A-B + C  A-C + B • Hydrolysis: Water reacts with organic compounds to split them into two smaller product molecules • (e.g.) A-B + H2O  A-H + B-OH

  4. A Variety of Reactions Among Organic Compounds (continues) • Condensation: A-H + B-OH  A-B + H2O • A-H + B-H  A-B + H2 (dehydrogenation) • Rearrangement: (e.g.) Isomerization. No Changes in Molecular Formula, but Just Rearrangement of Carbon Atoms

  5. Structural Formulas

  6. Bond-line structures are an extreme shorthand for representing molecules • C atoms are omitted but C-C bonds are illustrated in a zigzag arrangement • C-H bonds are omitted while bonds of C atoms to other atoms or molecular groups are shown explicitly

  7. Sometimes it will be important to distinguish the 3-D structure of a molecule Bond Below Plane Bond Above Plane

  8. Different Organic Compound Classes IUPAC Nomenclature Prefix / Parent / Suffix

  9. Alkanes are also called paraffins

  10. Alkanes with Side Chains • A normal alkane molecule minus one hydrogen atom is known as an alkyl group: The short hand for an alkyl group is R- • The names of the alkyl groups conform to the names of the corresponding alkanes

  11. Alkanes with Side Chains • Branched alkanes result when carbon atoms in the chain bond to other carbon atoms, forming side chains. CH3-CH2 _CH2-CH2-CH3 + H2 CH3-CH2-CH2-CH3 +CH4 CH3-CH-CH2-CH3+ H2 CH3 Same Chemical Formula of C5H12, but different carbon structures: Isomers

  12. Alkanes with Side Chains How to name alkanes with side chains? Step 1) Identify the longest continuous carbon chain (parent part of the IUPAC name) Step 2) Number carbon atoms along the main carbon chain - The lowest numbered carbon atom must appear at the end of the chain closest to the first branch chain Step 3) Identify side chains and locate them on the main chain Step 4) Combine “parent part” and “prefix part” More examples how to name alkanes with side chains

  13. C-H bonds are non-polar => Alkanes are non-polar • Alkanes are not soluble in water, a highly polar compound • The absence of polarity means that alkane molecules do not strongly interact

  14. Common Name is Ethylene

  15. The location of each double bond is indicated in the prefix and the subfix becomes -dienes

  16. - Both terminal carbon atoms can bond with terminal carbon atoms of other isoprenes to form a variety of cyclic and acyclic compounds with different degrees of saturation and various functional groups attached.

  17. They are responsible for the fragrant odors of pine trees and the bright colors of tomatoes and carrots. Three isoprene units => Isolated from roses Two isoprene units => A distinctive lemon odor

  18. Phenylalanine benzyl heptanoate

More Related