Synthetic Inorganic Chemistry

(John Hannent) #1
218 ELEMENTS OF GROUP III

precipitate remains unaffected, but after the NH4OH is all
neutralized (shown by the solution ceasing to smell of am-
monia after shaking) a little more acetic acid redissolves the
precipitate.

Ammonium hydroxide and acetic acid are of equal strength as
base and acid respectively. That the A1(OH) 3 does not dissolve
in excess NH4OH indicates that it is not a strong enough acid to
react with a base of this feeble strength. That it does dissolve
in acetic acid indicates that it is a strong enough base to react with
an acid of the feeble strength of acetic acid. Thus aluminum
hydroxide, although an extremely weak base, is more basic than
acidic.


  1. Instability of Aluminum Carbonate. Add together
    solutions of A1 2 (SO4) 3 and Na 2 CO 3. Effervescence takes
    place, and the escaping gas can be shown to be carbon dioxide.
    A gelatinous white precipitate is formed resembling previous
    precipitates of A1(OH) 3. To show whether this precipitate
    is really the hydroxide, or perhaps the carbonate or basic
    carbonate, collect some of it on a filter and wash it very
    thoroughly with water to remove any excess of Na 2 CO 3.
    Then add an acid (say HC1) to the precipitate and observe
    that it dissolves without a trace of effervescence.


Reference books tell us that aluminum carbonate has never
been prepared. In this experiment we brought together the ions
of aluminum carbonate and the result showed that this salt cannot
exist in solution. The reaction might be described as the hydroly-
sis of aluminum carbonate:
2A1+++ 3CO 3 ~~
6H 2 O^=;6OH" 6H+
I 1
2A1(OH) 3 3H 2 CO 3
1 I
2A1(OH) 3 i 3H 2 O + 3CO 21
That aluminum carbonate is thus completely hydrolyzed indicates
that the base and the acid are both very weak.

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