Online courses directory (13677)

nomenclature and reactions of amines. Amine Naming Introduction. Amine Naming 2. Amine as Nucleophile in Sn2 Reaction. Amine in Sn2 part 2. Sn1 Amine Reaction. Amine Naming Introduction. Amine Naming 2. Amine as Nucleophile in Sn2 Reaction. Amine in Sn2 part 2. Sn1 Amine Reaction.

aromatic compounds, naming derivatives of benzene, electrophilic aromatic substitution reactions. Naming Benzene Derivatives Introduction. naming benzene derivatives. Aromatic Compounds and Huckel's Rule. Aromatic Stability I. aromatic stability II. aromatic stability III. aromatic stability IV. aromatic stability V. Aromatic Heterocycles I. Aromatic Heterocycles II. Resonance. Electrophilic Aromatic Substitution. Bromination of Benzene. Friedel Crafts Acylation. Friedel Crafts Acylation Addendum. Electrophilic Aromatic Substitution Mechanism. Halogenation. Nitration. Sulfonation. Friedel-Crafts Alkylation. Friedel-Crafts Acylation. Ortho-Para Directors I. Ortho-Para Directors II. Ortho-Para Directors III. Meta Directors I. Meta Directors II. Multiple Substituents. Birch Reduction I. Birch Reduction II. Reactions at the Benzylic Position. Synthesis of Substituted Benzene Rings I. Synthesis of Substituted Benzene Rings II. Nucleophilic Aromatic Substitution I. Nucleophilic Aromatic Substitution II. Naming Benzene Derivatives Introduction. naming benzene derivatives. Aromatic Compounds and Huckel's Rule. Aromatic Stability I. aromatic stability II. aromatic stability III. aromatic stability IV. aromatic stability V. Aromatic Heterocycles I. Aromatic Heterocycles II. Resonance. Electrophilic Aromatic Substitution. Bromination of Benzene. Friedel Crafts Acylation. Friedel Crafts Acylation Addendum. Electrophilic Aromatic Substitution Mechanism. Halogenation. Nitration. Sulfonation. Friedel-Crafts Alkylation. Friedel-Crafts Acylation. Ortho-Para Directors I. Ortho-Para Directors II. Ortho-Para Directors III. Meta Directors I. Meta Directors II. Multiple Substituents. Birch Reduction I. Birch Reduction II. Reactions at the Benzylic Position. Synthesis of Substituted Benzene Rings I. Synthesis of Substituted Benzene Rings II. Nucleophilic Aromatic Substitution I. Nucleophilic Aromatic Substitution II.

naming carboxylic acids, formation of carboxylic acid derivatives. Carboxlic Acid Introduction. Carboxylic Acid Naming. Fisher Esterification. Acid Chloride Formation. Amides, Anhydrides, Esters and Acyl Chlorides. Relative Stability of Amides Esters Anhydrides and Acyl Chlorides. Amide Formation from Acyl Chloride. Carboxlic Acid Introduction. Carboxylic Acid Naming. Fisher Esterification. Acid Chloride Formation. Amides, Anhydrides, Esters and Acyl Chlorides. Relative Stability of Amides Esters Anhydrides and Acyl Chlorides. Amide Formation from Acyl Chloride.

conjugation, conjugated dienes, addition reactions of conjugated dienes, diels-alder reaction, MO theory, color. addition reaction of conjugated dienes I: mechanism. addition reaction of conjugated dienes II: example. addition reaction of conjugated dienes III: control. diels-alder I: mechanism. diels-alder II: endo vs exo. diels-alder III: stereochemistry of dienophile. diels-alder IV: stereochemistry of diene. diels-alder V: regiochemistry. diels-alder VI: more regiochemistry. diels-alder VII: intramolecular. intro to molecular orbital (MO) theory. MO theory for butadiene. MO theory for Diels-Alder. intro to color theory. conjugation and color. color in organic molecules. addition reaction of conjugated dienes I: mechanism. addition reaction of conjugated dienes II: example. addition reaction of conjugated dienes III: control. diels-alder I: mechanism. diels-alder II: endo vs exo. diels-alder III: stereochemistry of dienophile. diels-alder IV: stereochemistry of diene. diels-alder V: regiochemistry. diels-alder VI: more regiochemistry. diels-alder VII: intramolecular. intro to molecular orbital (MO) theory. MO theory for butadiene. MO theory for Diels-Alder. intro to color theory. conjugation and color. color in organic molecules.

A review of hybrid orbitals, dot structures, electronegativity, and polarity. sp3 Hybridized Orbitals and Sigma Bonds. Pi bonds and sp2 Hybridized Orbitals. dot structures I: single bonds. dot structures II: multiple bonds. sp3 hybrid orbitals. tetrahedral bond angle proof. sp2 hybrid orbitals. sp hybrid orbitals. more hybridization. electronegativity. electronegativity and intermolecular forces. sp3 Hybridized Orbitals and Sigma Bonds. Pi bonds and sp2 Hybridized Orbitals. dot structures I: single bonds. dot structures II: multiple bonds. sp3 hybrid orbitals. tetrahedral bond angle proof. sp2 hybrid orbitals. sp hybrid orbitals. more hybridization. electronegativity. electronegativity and intermolecular forces.

bond-line structures, functional groups, formal charges, resonance structures, oxidation and reduction, acid/base chemistry. bond-line structures. 3-D bond-line structures. structural (constitutional) isomers. functional groups I. functional groups II. formal charge I. formal charge II. resonance structures I. resonance structures II. resonance structures III. oxidation states I. oxidation states II. Acid/Base Definitions. Ka and pKa Derivation. Stabilization of Conjugate Base I. Stabilization of Conjugate Base II. Stabilization of Conjugate Base III. Stabilization of Conjugate Base IV. bond-line structures. 3-D bond-line structures. structural (constitutional) isomers. functional groups I. functional groups II. formal charge I. formal charge II. resonance structures I. resonance structures II. resonance structures III. oxidation states I. oxidation states II. Acid/Base Definitions. Ka and pKa Derivation. Stabilization of Conjugate Base I. Stabilization of Conjugate Base II. Stabilization of Conjugate Base III. Stabilization of Conjugate Base IV.

chirality, stereoisomers, assigning absolute configuration using the R,S system, optical activity, diastereomers, meso compounds, fischer projections. Introduction to Chirality. Chiral Examples 1. Chiral Examples 2. Cahn-Ingold-Prelog System for Naming Enantiomers. R,S (Cahn-Ingold-Prelog) Naming System Example 2. chirality centers and stereoisomers. R,S system for determining absolute configuration. R,S system for cyclic compounds. optical activity I: theory. optical activity II: calculations. Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds. diastereomers. meso compounds. fischer projections. Introduction to Chirality. Chiral Examples 1. Chiral Examples 2. Cahn-Ingold-Prelog System for Naming Enantiomers. R,S (Cahn-Ingold-Prelog) Naming System Example 2. chirality centers and stereoisomers. R,S system for determining absolute configuration. R,S system for cyclic compounds. optical activity I: theory. optical activity II: calculations. Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds. diastereomers. meso compounds. fischer projections.

SN1, SN2, E1, E2, nucleophiles, nucleophilicity, basicity. Naming Alkyl Halides. Sn2 Reactions. Sn1 Reactions. Steric hindrance. Sn2 Stereochemistry. Solvent Effects on Sn1 and Sn2 Reactions. Nucleophilicity (Nucleophile Strength). Nucleophilicity vs. Basicity. E2 Reactions. E1 Reactions. Zaitsev's Rule. Comparing E2 E1 Sn2 Sn1 Reactions. E2 E1 Sn2 Sn1 Reactions Example 2. E2 E1 Sn2 Sn1 Reactions Example 3. nucleophile/electrophile and The Schwartz Rules. alkyl halide nomenclature. SN1 reaction: mechanism. SN1 reaction: stereochemistry. SN2 mechanism and stereochemistry. SN1 vs SN2: solvent effects. SN1 vs SN2: summary. E1 Elimination: mechanism. E1 Elimination: regioselectivity and stereoselectivity. carbocations and rearrangements. E1 Elimination: carbocation rearrangements. E2 Elimination: mechanism. E2 Elimination: regioselectivity. E2 Elimination: stereoselectivity. E2 Elimination: stereospecificity. E2 Elimination: substituted cyclohexanes. nucleophilicity and basicity. SN1 SN2 E1 E2 reactions: primary and tertiary alkyl halides. SN1 SN2 E1 E2 reactions: secondary alkyl halides. Naming Alkyl Halides. Sn2 Reactions. Sn1 Reactions. Steric hindrance. Sn2 Stereochemistry. Solvent Effects on Sn1 and Sn2 Reactions. Nucleophilicity (Nucleophile Strength). Nucleophilicity vs. Basicity. E2 Reactions. E1 Reactions. Zaitsev's Rule. Comparing E2 E1 Sn2 Sn1 Reactions. E2 E1 Sn2 Sn1 Reactions Example 2. E2 E1 Sn2 Sn1 Reactions Example 3. nucleophile/electrophile and The Schwartz Rules. alkyl halide nomenclature. SN1 reaction: mechanism. SN1 reaction: stereochemistry. SN2 mechanism and stereochemistry. SN1 vs SN2: solvent effects. SN1 vs SN2: summary. E1 Elimination: mechanism. E1 Elimination: regioselectivity and stereoselectivity. carbocations and rearrangements. E1 Elimination: carbocation rearrangements. E2 Elimination: mechanism. E2 Elimination: regioselectivity. E2 Elimination: stereoselectivity. E2 Elimination: stereospecificity. E2 Elimination: substituted cyclohexanes. nucleophilicity and basicity. SN1 SN2 E1 E2 reactions: primary and tertiary alkyl halides. SN1 SN2 E1 E2 reactions: secondary alkyl halides.

Discover How To Improve Your Organic Gardening Soil

Como montar um bom script de venda e as planilhas e ferramentas mais usadas por vendedores de alto desempenho

A Practical Approach to Organizational Management

The free online course Organizational Change - Managing and Supporting Employees presents you with a practical step by step guide on the most effective and efficient way to implement organizational change and how to manage and support employees through what can be for many a very difficult period in their working lives. With continuous changes in technology and increased competition due to globalization, organizations need to be able to continuously adapt to the changes occurring around them or face the risk of becoming irrelevant in the market place. This course will help you develop the change management skills necessary to do so. First you will learn how to successfully manage organizational change. You will study 9 key success factors that research on successful organizational change projects from all over the world indicate are crucial for change to be fully implemented. Each of these 9 key success factors will focus on a specific element of organizational change such as: the role of stakeholders, the development of a change plan, and risk management strategies. Next you will learn how to guide employees through organizational change. You will study the 11 key success factors necessary to ensure that your employees do not have a negative experience during the change period. You will learn how to empathize with your employees and see change from their perspective, learn why stability is important during a period of change, and how to develop a policy of open communication throughout the process. This free course will be of great interest to professionals working in an industry that is currently experiencing, or will soon be experiencing change, and wish to play a prominent role in the change management process. The course will also be of interest to small business owners who wish to learn more about guiding their business and employees through a period of change.<br />

How to make Change successful by engaging everyone in the validated OCAI survey and working on culture + change in teams

Nick Earl, General Manager of Electronic Arts Redwood Shores Studio, talks about how the General Manager's job is t

Come Risparmiare Tempo e Fatica Usando Strumenti Internet Gratuiti

Non solo parole, ma anche 8 videolezioni. Il tuo modo di lavorare non sar

A vida que conhecemos só ocorre na Terra ? Pode existir vida em outros lugares do Universo? Para conhecer melhor a vida faz-se necessário conhecer outras vidas. Este curso explora questões abertas sobre a origem da vida em um contexto astronômico.

A Short Course Overview of the Background, Event, Panic and Legacy

A Psicologia é uma ciência relativamente recente, mas a preocupação do homem em desvendar os

This course is geared for Cisco's, CCNA (200-120) certification exam. Enter to win a 5 day CCNA bootcamp with me.