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  2. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    The table given below shows pKa values of various monosubstituted benzoic acids. pKa values of mono substituted benzoic acids [citation needed] Substituent

  3. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Benzoic acid is cheap and readily available, so the laboratory synthesis of benzoic acid is mainly practiced for its pedagogical value. It is a common undergraduate preparation. Benzoic acid can be purified by recrystallization from water because of its high solubility in hot water and poor solubility in cold water. The avoidance of organic ...

  4. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    The starting point for the collection of the substituent constants is a chemical equilibrium for which the substituent constant is arbitrarily set to 0 and the reaction constant is set to 1: the deprotonation of benzoic acid or benzene carboxylic acid (R and R' both H) in water at 25 °C. Scheme 1. Dissociation of benzoic acids

  5. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    Nitric acid, with a pK value of around −1.7, behaves as a strong acid in aqueous solutions with a pH greater than 1. [23] At lower pH values it behaves as a weak acid. pK a values for strong acids have been estimated by theoretical means. [24] For example, the pK a value of aqueous HCl has been estimated as −9.3.

  6. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    Monochloroacetic acid (pK a =2.82), though, is stronger than formic acid, due to the electron-withdrawing effect of chlorine promoting ionization. In benzoic acid, the carbon atoms which are present in the ring are sp 2 hybridised. As a result, benzoic acid (pK a =4.20) is a stronger acid than cyclohexanecarboxylic acid (pK a =4.87).

  7. 4-Hydroxybenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxybenzoic_acid

    4-Hydroxybenzoic acid, also known as p-hydroxybenzoic acid (PHBA), is a monohydroxybenzoic acid, a phenolic derivative of benzoic acid.It is a white crystalline solid that is slightly soluble in water and chloroform but more soluble in polar organic solvents such as alcohols and acetone. 4-Hydroxybenzoic acid is primarily known as the basis for the preparation of its esters, known as parabens ...

  8. 3-Chlorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Chlorobenzoic_acid

    3-Chlorobenzoic acid is an organic compound with the molecular formula ClC 6 H 4 CO 2 H. It is a white solid that is soluble in some organic solvents and in aqueous base. It is a white solid that is soluble in some organic solvents and in aqueous base.

  9. 4-Chlorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzoic_acid

    4-Chlorobenzoic acid is an organic compound with the molecular formula ClC 6 H 4 CO 2 H. It is a white solid that is soluble in some organic solvents and in aqueous base. 4-Chlorobenzoic acid is prepared by oxidation of 4-chlorotoluene .