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Problems involving addition of X2 (halogenation). Synthesis problems-utilizing radical halogenation, Vape Mods E2, SN2, oxidation (PCC), vape pen and Grignards for synthesis. Organic chemistry: "Some SN2, SN1, E2, and E1 topics". Natural chemistry: "Alcohols, oxidation, and reduction". Organic chemistry: "Electrophilic aromatic substitution". Organic chemistry: "Alkyne synthesis and reactions". Organic chemistry: "How to draw reasonable electron-pushing arrows".

Organic chemistry: "Aromaticity and Huckel's rule". Reaction of Grignard reagents as bases with protic solvents. Organic chemistry: "Alcohols". Reaction of alcohols with acids and bases. Organic chemistry: "Conjugated pi molecular orbitals". Radical halogenation via radical chain mechanisms. Organic chemistry: "Organometallics". Halogenation of alcohols (PBr3, SOCl2).

Natural chemistry: "Benzenes and phenols". Crystal structures of imidazolium bis(trifluoromethanesulfonyl)-imide ‘ionic liquid’ salts: the first organic salt with a cis-TFSI anion conformation.

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1.6 Maximum Power Point 1.7 Maximum Power Time 1.7.1 MPT definition 1.7.2 MPT empirical characterization Timing a discharge cycle From voltage sag 1.7.3 MPT derivation from specs From specification knowledge From discharge curves 1.7.4 Typical values of MPT 1.7.5 MPT conversions Internal collection resistance calculation Energy effectivity calculation Voltage sag calculation 1.7.6 Using the MPT 1.8 States 1.8.