Dihydroxylation - Study guides, Class notes & Summaries

HX - Hydrohalogenation - Markovnikov addition - Neither syn / anti - H + X added HBr/H2O2 or ROOR - Hydrobromination - Anti-markovnikov - Neither Syn / Anti - H + Br 00:13 00:54 H2, Pt or Pd - Hydrogenation - No markovnikov - Syn addition - H + H H3O+ - Acid-catalyzed hydration - Markovnikov addition - Syn addition - H + OH 1) Hg(OAc)2, H2O 2) NaBH4, NaOH - Oxymercuration-Demercuration - Markovnikov Addition - No Syn or Anti - H + OH - No Carbo...

Chapter 7 is a two week long chapter that introduces substitution and elimination reactions. Students will learn the reaction mechanisms for Sn1, Sn2, E1 and E2 reactions. They will also begin to understand the difference between protic and aprotic solvents, as well as what reagents are weak or strong nucleophiles and/or weak or strong bases. Understanding this concept will allow students to decide when a reaction will be an elimination and/or substitution reaction. These notes provide in-depth ...

preparation of aldehydes and ketones from common reagents via oxidation or reduction

These are commonly missed questions and answers from the Organic Chemistry I class.

Following document includes REACTION MECHANISMS, definitions, explanations, prequisites and a lot more !! - Describing Polar Organic Reactivity and Stereochemistry - Functionalisation of Alkenes - Organometallic Nucleophiles - Reactions of Epoxides - Synthesis and Reactivity of Carbonyl Compounds - Multistep Syntheses of Interesting Molecules More in-depth: - Electrophilic addition of asymmetrical & symmetrical reagents - Alkene halogenation - Bromination of cycloalkenes - Inte...