'Substituents' diaporamas de présentation

Chapter 18 Carboxylic Acids

Chapter 18 Carboxylic Acids. Carboxylic Acid Nomenclature. O. HCOH. O. CH 3 COH. O. CH 3 (CH 2 ) 16 COH. Table 18.1 . systematic IUPAC names replace "-e" ending of alkane with "oic acid". Systematic Name. methanoic acid. ethanoic acid. octadecanoic acid. O. HCOH. O. CH 3 COH. O.

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Patrick An Introduction to Medicinal Chemistry 3/e Chapter 13

Patrick An Introduction to Medicinal Chemistry 3/e Chapter 13 QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS (QSAR). Contents 1. Introduction 2. Hydrophobicity of the Molecule (4 slides) 3. Hydrophobicity of Substituents (2 slides) 4. Electronic Effects

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Patrick An Introduction to Medicinal Chemistry 3/e Chapter 13

Patrick An Introduction to Medicinal Chemistry 3/e Chapter 13 QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS (QSAR). Contents 1. Introduction 2. Hydrophobicity of the Molecule (4 slides) 3. Hydrophobicity of Substituents (2 slides) 4. Electronic Effects

831 views • 63 slides

Aldehyde and Ketones

Aldehyde and Ketones. Course Outcomes Involved. CO #3: Ability to DEMONSTRATE the reactions involving alcohol, ether, aldehyde , ketone , carboxylic acid and aromatic compounds. Outlines. Naming of Aldehyde and Ketones Relative Reactivity of Carbonyl Group

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Chapter 16 Carboxylic Acids and Esters

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Chapter 10 Introduction to Organic Chemistry: Alkanes

Chapter 10 Introduction to Organic Chemistry: Alkanes. 10.3 Alkanes with Substituents. Isomers of Butane. Isomers have the same molecular formula. have different atom arrangements. of butane (C 4 H 10 ) are a straight chain and a branched chain. Alkyl groups. Alkyl groups are

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Introduction to Organic Chemistry: Alkanes

Introduction to Organic Chemistry: Alkanes. Alkanes with Substituents. Isomers of Butane. Isomers have the same molecular formula. have different atom arrangements. of butane (C 4 H 10 ) are a straight chain and a branched chain. Alkyl groups. Alkyl groups are

437 views • 16 slides

5.4 HYDROGEN ATOM DONORS

5.4 HYDROGEN ATOM DONORS. Reduction by hydrogen-atom donors involves free-radical intermediates. Tri- n -butyltin hydride is the most prominent example of this type of reducing agent. It is able to reductively replace halogen by hydrogen in organic compounds.

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Patrick An Introduction to Medicinal Chemistry 3/e Chapter 22 ANTIULCER AGENTS

Patrick An Introduction to Medicinal Chemistry 3/e Chapter 22 ANTIULCER AGENTS Part 3: Proton pump inhibitors. Contents Part 3: Proton pump inhibitors 23. Parietal Cells and the Proton Pump 24. Proton Pump Inhibitors 25. Mechanism of inhibition 26. Design of omeprazole (Losec)

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Patrick An Introduction to Medicinal Chemistry 3/e Chapter 22 ANTIULCER AGENTS

Patrick An Introduction to Medicinal Chemistry 3/e Chapter 22 ANTIULCER AGENTS Part 3: Proton pump inhibitors. Contents Part 3: Proton pump inhibitors 23. Parietal Cells and the Proton Pump 24. Proton Pump Inhibitors 25. Mechanism of inhibition 26. Design of omeprazole (Losec)

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Naming of Alkanes, Cycloalkanes, and Alkyl Halides

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Patrick An Introduction to Medicinal Chemistry 3/e Chapter 22 ANTIULCER AGENTS

Patrick An Introduction to Medicinal Chemistry 3/e Chapter 22 ANTIULCER AGENTS Part 3: Proton pump inhibitors. Contents Part 3: Proton pump inhibitors 23. Parietal Cells and the Proton Pump 24. Proton Pump Inhibitors 25. Mechanism of inhibition 26. Design of omeprazole (Losec)

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Some New Allotropes

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Substituent Effects: Electrophilic Aromatic Substitution

Substituent Effects: Electrophilic Aromatic Substitution. Substituents that are capable of donating electrons into the benzene ring will stabilize both the carbocation intermediate and the transition state leading to its formation Increases the rate of electrophilic aromatic substitution

534 views • 10 slides