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Wednesday, December 18, 2019

Titration of Borax: Tincal : Suhaga :


When Borax dissolved in water, it is subject to completely dissociate, and then, hydrolyzes to orthoboric acid (B(OH)3  and [B(OH)4]anions,  and resulting PH  of  solution about 9.13.
According to the equation:
Na2[B4O5(OH)4]8H2O(s)2Na+(aq) + B4O5(OH)42− (aq) + 8H2O(l)
B4O5(OH)42−(aq) + 5H2O(l) 4 B(OH)3(aq) + 2OH(aq)

The liberated B(OH)3(aq)  acts as a Lewis acid on OH ions from auto ionization of water, and hence, in equilibrium with water:
B(OH)3(aq)+2H2O(l) B(OH)4(aq) + H3O+(aq)

Therefore, one mole of borax reacts with two moles of strong acid solutions. This is  because when Borax dissolved in water Both B(OH)3(aq)  and B(OH)4(aq) are formed but only  B(OH)4(aq) react with acid.  
For example:
                Na2[B4O5(OH)4].8H2O(aq) + 2HCl(aq) 4B(OH)3(aq)+ 2NaCl (aq) + 5 H2O

ILLUSTRATIVE EXAMPLE: Aqueous solution of borax reacts with two moles of acids.
This is because of:
(A) Formation of 2mol of B(OH)3 only
(B) Formation of 2mol of Na[B(OH)4]¯ only
(C) Formation of 1mol each of B(OH)3 and Na[B(OH)4
(D) Formation of 2mol each of Na[B(OH)4]¯and B(OH)3 of which only Na[B(OH)4]¯ reacts with acid.
Answer: (D)
Solution: 
 Na2B4O7 + 7H2O 2B(OH)3 + 2Na[B(OH)4]
B(OH)3 or H3BO3 is an acid and does not react with acid. Hence Na[B(OH)4] reacts with acid.

What is structure of Borax: Tincal or Suhaga ?

The name borax is derived from the Persian word borak, meaning white. IUPAC name of borax is sodium tetraborate decahydrate (Na2B4O710 H2O ). Also note that, after analyzing its crystal structure, borax is more properly formulated as Na2[B4O5(OH)4]8H2O
Structure:
(1) It is also named as sodiumtetra borate decahydrate
(2) Common Indian name is Suhaga.
(3) Na2B4O7. 5H2O is known as Jeweller's Boran
(4) Na2B4O7 is known as Boron glass
(5) It is also represent as Na2O.2B2O3.10H2O.
IIT UPDATE: (2016):

Titration of Boric Acid:


Boric acid is a weak monoprotic acid (Ka=6.4×10−10). Therefore, it cannot be directly titrated with standard strong alkali (NaOH). But by the addition of an organic poly hydroxy compound such as 1,2- or 1,3-diol, (Like Sugar, Mannitol, Catechol)  it is converted to a much stronger acid, which can be titrated using phenolphthalein. This is due to the complex formation between hydrated borate ion and either 1,2- or 1,3-diol  for example .

Ploy hydroxy (Cis-diol) increases acidity of boric acid due to formation of complex with metaborate and reaction goes to farward to produce more H+.
IIT UPDATE: (2006):