'Sn2 mechanism' diaporamas de présentation

Reactions of Alcohols

Reactions of Alcohols. Oxidation R-X, Ether, and Ester Preparation Protection of Alcohols Synthesis The Logic of Mechanisms. Alcohols are Synthetically Versatile. Oxidation levels of oxygen- halogen- and nitrogen- containing molecules. Oxidation - Reduction.

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HL organic chemistry topic 20

HL organic chemistry topic 20. More functional groups Amines NH 2 Draw 1-aminopropane (propanamine) and give condensed formula. Methylamine (old) aminomethane IUPAC 1,6-diaminohexane. 1-butylamine, 1-butanamine, 1-aminobutane (all the same). Secondary amines.

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Fischer-Rosanoff Convention

Fischer-Rosanoff Convention. Before 1951, only relative configurations could be known. Sugars and amino acids with same relative configuration as (+)-glyceraldehyde were assigned D and same as (-)-glyceraldehyde were assigned L.

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S N 1 Reactions

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Organic Synthesis Notation

Organic Synthesis Notation. Chemistry Advanced Higher . Organic molecule synthesis. The construction of compounds via organic reactions. All chemical reactions involve the breaking and making of bonds. Curly arrows give an impression of bonds breaking and bonds being made.

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8.3 The S N 2 Mechanism of Nucleophilic Substitution

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1. 2-methyl-2-propanol, t -butyl alcohol

D. PAVIA CHEM 352. ANSWERS EXAM TWO. 1. 2-methyl-2-propanol, t -butyl alcohol. cyclopentanol, cyclopentyl alcohol. methoxybutane, butyl methyl ether. ethoxycyclobutane, cyclobutyl ethyl ether. 1-methyl-2-cyclopentenol. 1,2-cyclopentanediol. 2. a) aprotic solvent, Cl > Br.

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D. PAVIA CHEM 352

D. PAVIA CHEM 352. SAMPLE EXAM TWO. 1. Name the following compounds by both IUPAC and common names, except as noted. IUPAC. COMMON. IUPAC. COMMON. omit. omit. 2. From the following pairs, pick (circle) the one from each pair that is:. a) the best nucleophile in DMSO.

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