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Acetic acid, CH 3 COOH, is an acid because it donates a proton to water (H 2 O) and becomes its conjugate base, the acetate ion (CH 3 COO −). H 2 O is a base because it accepts a proton from CH 3 COOH and becomes its conjugate acid, the hydronium ion, ( H 3 O + ).
A conjugate acid, within the Brønsted–Lowry acid–base theory, is a chemical compound formed when an acid gives a proton (H +) to a base—in other words, it is a base with a hydrogen ion added to it, as it loses a hydrogen ion in the reverse reaction.
In chemistry, an acid–base reaction is a chemical reaction that occurs between an acid and a base.It can be used to determine pH via titration.Several theoretical frameworks provide alternative conceptions of the reaction mechanisms and their application in solving related problems; these are called the acid–base theories, for example, Brønsted–Lowry acid–base theory.
For example, acetic acid is a weak acid which has a = 1.75 x 10 −5. Its conjugate base is the acetate ion with K b = 10 −14 /K a = 5.7 x 10 −10 (from the relationship K a × K b = 10 −14), which certainly does not correspond to a strong base. The conjugate of a weak acid is often a weak base and vice versa.
The first row shows the reaction, which some authors label R and some leave blank. The second row, labeled I, has the initial conditions: the nominal concentration of acid is C a and it is initially undissociated, so the concentrations of A − and H + are zero. The third row, labeled C, specifies the change that occurs during the reaction.
For example, anhydrous acetic acid (CH 3 COOH) as solvent is a weaker proton acceptor than water. Strong aqueous acids such as hydrochloric acid and perchloric acid are only partly dissociated in anhydrous acetic acid and their strengths are unequal; in fact perchloric acid is about 5000 times stronger than hydrochloric acid in this solvent. [3]
acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...
For aqueous solutions of an acid HA, the base is water; the conjugate base is A − and the conjugate acid is the hydronium ion. The Brønsted–Lowry definition applies to other solvents, such as dimethyl sulfoxide : the solvent S acts as a base, accepting a proton and forming the conjugate acid SH + .