1 / 20

Drawing Organic Structures

Drawing Organic Structures. Organic compounds are held together by covalent bonds a covalent bond may be represented by a pair of dots, or by a single line. Molecular formula. Use methane as an example CH 4 molecular formula shows relative numbers of atoms

vinny
Download Presentation

Drawing Organic Structures

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. Drawing Organic Structures • Organic compounds are held together by covalent bonds • a covalent bond may be represented by a pair of dots, or by a single line

  2. Molecular formula • Use methane as an example • CH4 • molecular formula • shows relative numbers of atoms • conveys no sense of structure or bonding • conveys no sense of chemistry

  3. Writing Molecular Formulas • The number of carbon atoms is specified first • The number of hydrogen atoms is specified next • The remaining atoms are then specified in (usually alphabetical) order • cyclohexane: C6H12 • benzoic acid: C7H6O2 • ethyl para-aminobenzoate: C9H11NO2 • picryl chloride: C6H2ClN3O6

  4. Full structural formula • every atom specified • every bond explicitly shown • methane is simple • two structures convey the same information about as efficiently

  5. Now lets try it with cholesterol as the example… • Molecular formula • C27H46O

  6. Full structural formula

  7. How do we simplify this? • recognize that every organic compound contains carbon • delete the symbol for carbon atoms except for those explicitly involved in a functional group (CHO, COOH, CN)

  8. Lets do it…

  9. Can we make it simpler…? • We have removed all the carbon symbols (every organic compound contains carbon) • Practically every carbon compound contains hydrogen • delete symbol for hydrogen except where it is part of a functional group (e.g. CHO, OH)

  10. Lets try that… • Dramatic simplification • structural features are visible • three rings • length and shape of side chains

  11. Lets try that… • Dramatic simplification • structural features are visible • functional groups are visible • OH group of alcohol • C=C double bond

  12. Lets try that… • Dramatic simplification • structural features are visible • functional groups are visible • information is more available • how long does it take to find the important features?

  13. The molecules of this experiment • cyclohexane • C6H12 • toluene • C7H8 • benzoic acid • C7H6O2 • ethyl para-aminobenzoate • C9H11NO2

  14. Properties • all electrically neutral • all soluble in non-polar solvents (e.g. ether) • none soluble in water to an appreciable degree • cyclohexane & toluene are liquids • benzoic acid and ethyl para-aminobenzoate are solids

  15. Benzoic acid • a carboxylic acid • has one acidic hydrogen • weak acid • only slightly ionized • pKa ≈ 4 • reacts with base to give benzoate anion and water

  16. benzoic acid molecules are converted by strong base into benzoate anions • benzoate anions are converted by strong acids into benzoic acid molecules

  17. benzoic acid neutral, covalent molecules soluble in non-polar solvents (e.g. ether) almost insoluble in water sodium benzoate sodium cations and benzoate anions almost insoluble in non-polar organic solvents (e.g. ether) soluble in water A comparison

  18. Ethyl para-aminobenzoate • has both ester (neutral) and amine (base) functional groups • has one basic nitrogen • weak base: gives practically no OH— in water • reacts with acid to give alkylammonium cation

  19. ethyl p-aminobenzoate molecules are converted by strong acid into alkylammonium cations • the alkylammonium cations are converted by strong bases into ethyl p-aminobenzoate molecules

  20. ethyl p-aminobenzoate neutral, covalent molecules soluble in non-polar solvents (e.g. ether) almost insoluble in water the alkylammonium salt alkylammonium cations and sulfate or chloride anions almost insoluble in non-polar organic solvents (e.g. ether) soluble in water A comparison

More Related