Chemistry Assignment – 3 hours to complete Based off of the following chapters. Electrons, Bonds and Molecular Properties and their Representations Acids and Bases Alkanes and cycloalkanes Stereoch

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Chemistry Assignment – 3 hours to complete Based off of the following chapters.

Electrons, Bonds and Molecular Properties and their Representations

Acids and Bases

Alkanes and cycloalkanes

Stereochemistry: Enantiomers, Diastereomers, Symmetry and chirality, Racemic mixtures etc

Chemical reactivity and mechanisms: Carbocation rearrangements

Substitution reactions

Alkenes: Structure, Synthesis and their reactions

Alkynes: Structure, Synthesis and their reactions

Organic Synthesis

Chemistry Assignment – 3 hours to complete Based off of the following chapters. Electrons, Bonds and Molecular Properties and their Representations Acids and Bases Alkanes and cycloalkanes Stereoch
Final Assignment: Reactions and Mechanisms you should know all of the following reactions for the final exam, including substrates, reagents and products, and aspects of regio-and stereoselectivity. The extent to which you should know the mechanism is indicated in each case. Substitutions and Eliminations: SN1 (all types/aspectscovered, including carbocation rearrangements, full mechanisms) SN2(all types/aspectscovered, full mechanisms) E1(all types/aspectscovered, including carbocation rearrangements, full mechanisms) E2(all types/aspectscovered, full mechanisms) Alkenes: Markownikov Hydrohalogenation, including carbocation rearrangements (full mechanisms) Non-Markownikov Hydrohalogenation, (not the mechanism) Acid catalyzed hydration (full mechanism) Oxymercuration (mechanism, except for NaBH4step) Hydroboration-oxidation (full mechanism) Catalytic hydrogenation (not the mechanism) Dihalogenation (full mechanism) Halohydrin formation (full mechanism) Epoxidation with mCPBA (full mechanism) Acid catalyzed ring opening of epoxides with water (full mechanism) OsO4dihydroxylation (not the mechanism) Ozonolysis (not the mechanism) Alkynes: Markownikov Hydrohalogenation (full mechanism) Non-Markownikov Hydrohalogenation, (not the mechanism) Oxymercuration/hydration (full mechanism) Hydroboration-oxidation (full mechanism) Catalytic hydrogenation to alkanes (not the mechanism) Catalytic hydrogenation to alkenes (not the mechanism) Dissolvingmetal reduction to alkenes (full mechanism) Di-and tetra-halogenationusing dihalides (full mechanism) Ozonolysis (not the mechanism) Double elimination of dihalides (full mechanism) Alkylation of terminal alkynes (full mechanism

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