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Hydrogen bonding continued carboxylic acid dimers

Carboxylic acids are very soluble in alcohols because the acids form hydrogen bonds with alcohols. Also, alcohols are not as polar as water, so the longer-chain acids are more soluble in alcohols than they are in water. Most carboxylic acids are quite soluble in relatively nonpolar solvents such as chloroform because the acid continues to exist in its dimeric form in the nonpolar solvent. Thus, the hydrogen bonds of the cyclic dimer are not disrupted when the acid dissolves in a nonpolar solvent. [Pg.944]


See other pages where Hydrogen bonding continued carboxylic acid dimers is mentioned: [Pg.111]    [Pg.541]    [Pg.507]    [Pg.2553]    [Pg.102]    [Pg.384]    [Pg.155]    [Pg.171]    [Pg.164]   
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Acid continued) carboxylic

Acidity continued

Acids continued

Acids dimeric

Bond carboxylic

Bonding carboxylic acids

Bonding continued)

Bonding dimers

Bonds - continued

Bonds carboxylic acids

Carboxylates dimeric

Carboxylic acid dimeric

Carboxylic acid dimers

Carboxylic acids dimerization

Carboxylic acids hydrogen bonding

Carboxylic acids hydrogen bonds

Carboxylic acids hydrogenation

Carboxylic dimer

Dimer acid

Dimers hydrogen bonding

Hydrogen bond acidic

Hydrogen bond acidity

Hydrogen bond dimers

Hydrogen bonding (continued

Hydrogen bonding (continued acids

Hydrogen carboxylic acid

Hydrogen continued

Hydrogen-bonded acids

Hydrogen-bonded dimers

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