chapter 2 phenols
DESCRIPTION
Chapter 2 Phenols. 1-Nomenclature of Phenols. Phenols are compounds that have hydroxyl group bonded directly to benzene ring. Named on basis of phenol as parent, substituents listed in alphabetical order. 2-Physical Properties. - PowerPoint PPT PresentationTRANSCRIPT
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1-Nomenclature of PhenolsPhenols are compounds that have hydroxyl
group bonded directly to benzene ring.
Named on basis of phenol as parent, substituents listed in alphabetical order.
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OH
OH
1- Naphthol 2- Naphthol
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2-Physical Properties1-The OH group of phenols allows hydrogen bonding to other phenol molecules and to water.
2-Compared to compounds of similar size and molecular weight, hydrogen bonding in phenol raises its melting point, boiling point, and solubility in water.
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HH OOOO
Hydrogen Bonding of Phenols
Hydrogen Bonding with Water
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3- Acidity of PhenolsMost characteristic property of phenols is their acidity.
Phenols(pKa = 10) are more acidic than alcohols(pKa = 16-20) but less acidic than Carboxylic acids (pKa = 5).
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To explain why, let’s compare the ionization of Ethanol and Phenols
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Substituent Effects on the Acidity of Phenols.
1-Electron-releasing groups ( CH3, OCH3) have little or no effect.
2-Electron-withdrawing groups ( NO2, Cl, OH) increase acidity.
3- Multiple substituent of electron- withdrawing group greatly increase acidity of phenols.
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OH OH
CH3 OCH3
OH
OH OH
Cl NO2
OH
Electron-releasing groups have little or no effect.
Electron-withdrawing groups increase acidity.
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Effect of electron-withdrawing groups is mostpronounced at ortho and para positions.
OH OH OH
NO2
NO2
NO2
Effect of strong electron-withdrawing groups is cumulative.
OH OH OH
NO2NO2
NO2
NO2
NO2O2N
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4-Sources of PhenolsPhenols was first isolated from coal tar.Phenol is an important industrial chemical.Major use is in phenolic resins for adhesives and plastics.
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Industrial preparation of Phenols
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Laboratory Synthesis of Phenols
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5- Reactions of PhenolsA hydroxyl group is very powerful activating substituent, and electrophilic aromatic substitution in phenol occurs far faster, and under milder condition, than in benzene.a- Halogenation
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b- Sulfonation
c- Nitration
d- Nitrosation
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d-Friedal Crafts Alkylation
e-Friedal Crafts Acylation
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In the absence of ALCL3, However O-acylation occurs instead.
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f- Reaction with arenediazonium salts.
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6- Aspirin and the Klobe – Schmitt Reaction.
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Preparation of Salicylic Acid
This reaction is called the Kolbe- Schmitt reaction.Acidification coverts the sodium salt shown above to salicylic acid.