1. SELF.ORG.CHEM LECTURES THIS SAMPLE PRESENTATION IS 13 SLIDES LONG ABOUT 6 MIN READING EFFECTS AND SLIDES ADVANCE ARE AUTOMATIC EXCEPT WHEN INSTRUCTED TO CLICK HOWEVER, IN THE FULL LECTURE THESE ARE MANUALLY ACTIVATED FOR COMPLETE CONTROL BY LECTURER

2. SELF.ORG.CHEM LECTURES COMMON FUNCTIONAL GROUPS IN ORGANIC COMPOUNDS SELF-ORG.CHEM © Miguel E. Alonso-Amelot 2011 LECTURE SAMPLE

3. PROBLEM SHEET DETAILED SCRIPT TEXT FOR EACH SLIDE TO BE USED BY LECTURER IN CLASS SELF-ORG.CHEM INSTRUCTIONS FOR BEST RESULTS 21 INTERACTIVE SLIDES ON CLEAR BAKCGROUND SELF.ORG.CHEM LECTURES 3 MATERIALS INCLUDED IN THIS PACKAGE: 1234 Click mouse

4. 2 Why this is important SELF-ORG.CHEM Functional groups concentrate the majority of chemical properties and reactivity of organic compounds. Recognizing the reactive centers from their structural types and assigning the proper nomenclature is an essential part of the language of organic chemistry. 1 Most courses do not put enough emphasis on this fundamental subject, offering it as a bare unenthusiastic memory exercise only. Here we offer a lecture with a systematic, chemical approach to functional group recognition and naming. 34 4

5.  -unsatd ketone Thiol Peroxide Enol ether Alkyl halide Aminoacid THE HOT SPOTS A HAPLESS CARBON BACKBONE FUNCTIONAL GROUPS WAKE UP THE MOLECULE FUNCTIONAL GROUPS ARE WHERE THE ACTION IS 5 SELF-ORG.CHEM

6. USUALLY STUDENTS ARE REQUIRED TO LEARN BY HEART LONGT LISTS OF FUNCTIONAL GROUPS AND THEIR NAMES A DEADLY BORING AND DISCOURAGING PROPOSITION FOR BEGINNERS! WHY DO THEM SOMETHING LIKE THIS: SELF-ORG.CHEM 6

7. FUNDAMENTAL FUNCTIONAL GROUPS YOU CAN’T DO WITHOUT SELF-ORG.CHEM ALCOHOL ETHER AMINE ALKYL HALIDE ALKENE ALKYNE ARYL ALDEHYDE KETONE CARBOXYLIC ACID (ESTER) AMIDE ACYL HALIDE 7

8. ALTHOUGH MEMORIZING IS NECESSARY ONE CAN REACH THE SAME GOAL USING ORGANIC CHEMISTRY PRINCIPLES… …SYSTEMATICALLY AND INTELLIGENTLY SELF-ORG.CHEM HERE IS HOW 8

9. SELF-ORG.CHEM Bonding Patterns define Functional groups C=C C X C=X C XC Z = C = X X,Y,Z = N,O,S C X Y C=X Y SELF-ORG.CHEM SYSTEMATICS C XZ C≡C All functional groups fall within these bonding types 9

10. C bonded to N, O, S, Halogens ALCOHOLS, CARBINOLS ETHERS AMINES HALIDES (fluorides, chlorides…) THIOLS (mercaptans) SULFIDES (thio-ethers) ( F, Cl, Br, I ) SELF-ORG.CHEM C X FROM THE MOST SIMPLE 10

11. CARBONATE CARBAMATE UREAS GUANIDINE C=X Y Z X, Y, Z = N, O, S Highest Oxidation Level TO MORE COMPLEX SELF-ORG.CHEM EXPLAINED STEP BY STEP 11

12. PROBLEM SHEET DETAILED SCRIPT TEXT FOR EACH SLIDE TO BE USED BY LECTURER IN CLASS SELF-ORG.CHEM INSTRUCTIONS FOR BEST RESULTS 21 INTERACTIVE SLIDE LECTURE WITH FULL CONTROL SELF.ORG.CHEM LECTURES 12 THIS IS WHAT YOU GET IN THIS PACKAGE: 1234

13. TO ORDER THE COMPLETE LECTURE: CONTACT ADDITIONAL LECTURES IN OUR WEBSITE: END OF SAMPLE 13 SELF.ORG.CHEM LECTURES THANK YOU!