meta-directing. Reactions: Electrophilic aromatic substitution rxns‚ Nucleophilic aromatic substitution rxns (via benzyne or substitution-elmination)‚ Diels-Alder (endo/exo‚ inter/intramolecular)‚ Diene 1-2 and 1-4 electrophilic addition‚ Eliminating bromine from arenes via Grignard‚ Carboxylation of arenes via Grignard 4 Properties of: Amines (pkAs and resonance structures for aromatic and aliphatic molecules)‚ amides (sp2 hybridized by amide bonds)‚ anilines (aromatic amines) Structure of: Sugars
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Compounds containing aromatic groups are widespread in nature‚ and for this reason chemists who aim to synthesize naturally occurring compounds in the laboratory often need to introduce substituents to aromatic rings. In the organic synthesis laboratory‚ electrophilic aromatic substitutions which result in the formation of new carbon-carbon bonds are called ‘Friedel-Crafts’ alkylations and acylations‚ named for Charles Friedel of France and James Crafts of the United States‚ who together developed
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Introduction: The theory behind the extraction of a solution containing benzoic acid‚ cellulose‚ and methyl orange involves many components pertaining to the fundamental ideas of solubility and polarity. Using the concepts of like dissolving like and acid base reactions‚ a solution of organic acid (benzoic acid)‚ a water soluble compound cellulose‚ and an organic soluble compound methyl orange‚ can be separated and benzoic acid can be isolated by a method of extraction. At the fundamental
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bonding capacity of the hydroxyl group. Threonine‚ an essential amino acid‚ is a hydrophilic molecule. Threonine is an other hydroxyl-containing amino acid. It differs from serine by having a methyl substituent in place of one of the hydrogens on the β carbon and it differs from valine by replacement of a methyl substituent with a hydroxyl group. Note that both the α and β carbons of threonine are optically active. Cysteine is one of two sulfur-containing amino acids; the other is methionine. Cysteine
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polyhalogen compounds. Haloalkanes and Haloarenes Haloarenes Halogenated compounds persist in the environment due to their resistance to breakdown by soil bacteria. 10 Unit The replacement of hydrogen atom(s) in a hydrocarbon‚ aliphatic or aromatic‚ by halogen atom(s) results in the formation of alkyl halide (haloalkane) and aryl halide (haloarene)‚ respectively. Haloalkanes contain halogen atom(s) attached to the sp3 hybridised carbon atom of an alkyl group whereas haloarenes contain halogen
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ARYL HALIDES General formula: Ar–X where X = F‚ Cl‚ Br or I Examples Structure: C-X bonds are shorter and stronger Bond C-Cl C-Br Ar-X 1.69 A° 1.86 A° R-X 1.77 1.91 Dipole moments are unusually small. Bond C-Cl Preparation: 1. electrophilic aromatic substitution – useful only if one product is obtained C-Br Ar-X 1.7 D 1.7 D R-X 2.10 D 2.15 D Dipole moments may cancel out depending on the geometry of the molecule. 1 3/22/2012 PHYSICAL PROPERTIES: Boiling points – similar
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Introduction Extraction is a purification technique used in organic chemistry to separate compounds from a mixture of two or more compounds. There are three different extraction techniques: liquid-liquid extraction‚ solid-liquid extraction and chemically active extraction. All three types of extraction follow the same principle. Organic molecules dissolve in organic solvents and polar molecules dissolve in aqueous solvents. This phenomenon is observed because of the intermolecular forces between
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In the first part of this experiment acetic anhydride was used to prepare acetanilide which could then be readily brominated to form a mono-brominated product‚ with the bromine positioned at either the ortho‚ meta or para position on the aromatic ring. Acetic anhydride is very reactive towards nucleophiles and this reactivity is the result of the difference in electronegativities of the carbon and oxygen atoms that are bonded in acetic anhydride. This difference in electronegativities causes one
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napthalene and toulene were given to serve as reference standards to characterize and distinguish four unknown given samples. Nitration‚ bromine and basic oxidation testswere conducted to classify the different samples from being an aliphatic‚ or aromatic‚ saturated or unsaturated and alkylated or non-alkylated hydrocarbons. The physical state and color were noted by simple physical observation. The unknown samples were characterized and differentiated by using the three different tests to distinguish
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3 4 5 6 6 7 7 5 2 4 1 3 B. Applying the Chain Length Rule the NUMBERS are called "locators" items in BLUE are called "substituents". the name in RED at the end is called the suffix. 9 7 8 6 5 3-methyl heptane 4 3 This also applies for subsequent substituents‚ if either direction would give the same number. 2 1 The purpose of this sheet is to demonstrate the rules by which alkanes are named. 4-ethyl-6-methylnonane ORDER OF BUSINESS
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