CHM 315 Final: CHEM 315 Cal Poly Panoma 315 Final sp 2009
Document Summary
Credit: nomenclature (1, short syntheses (5, can be done in 3 steps, reactions page, using reactions learned thus far (30, mechanism in acid and mechanism in base, tautomers (in acid and in base) and drawing additional. Tautomer structures: 14c synthesis (1, sn1/e1 and sn2/e2 reactions. Pushing, carbocations, rearrangements: alkene reactions (regioselect. , stereoselect. ) It has been designed so that no one question will make or break you. The best strategy is to work steadily, starting with those problems you understand best. You do not get any points for writing wrong information or blank pages. Make sure you show all of your work. Draw in any lone pairs of electrons, formal charge and curved arrows to show electron movement in mechanism and explanation problems. If resonance is part of an answer, draw the best resonance structure, plus at least one additional resonance structure to show that resonance is present. Only write answers on the front of each page.
