O
H ClO
H ClOO
H ClOOO
H Cl
OOOiii. Di or pyrosulfuric acid, H 2 S 2 O 7HO S
HOOSHOO S
HOOOTable 7.8 Oxoacids of halogens
oxidation state
of XGeneric
nameOxoacids of
fluorineOxoacids of
chlorineOxoacids of
bromineOxoacids of
iodine
+1 Hypohalous
acid (HXO)HOF HOCl HOBr HOI+3 Halous acid
(HXO 2 )- HOClO - -
+5 Halic acid
(HXO 3 )- HOClO 2 HOBrO 2 HOIO 2
+7 Perhalic acid
(HXO 4 )- HOClO 3 HOBrO 3 HOIO 3
iv. Peroxy monosulfuric acid, H 2 SO 5
v. Peroxy disulfuric acid, H 2 S 2 O 8
vi. Thiosulfuric acid, H 2 S 2 O 3
7.8.2 Oxoacids of halogens : :Halogens form
several oxoacids (See Table 7.8). Only four
oxoacids have been isolated in pure form:
hypofluorous acid (HOF), perchloric acid
(HClO 4 ), iodic acid (HIO 3 ), metaperiodic acid
(H 2 IO 6 ). The others are stable only in aqueous
solutions or in the form of their salts.
The acid strength of the halogen oxoacids
increases with the increasing oxidation state of
halogen. For example, acid strength increases
from HClO, a weak acid (Ka = 3.5 × 10 -8), to
HClO 4 , a very strong acid (Ka>>1).
Strucutres of oxoacids of chlorine :
i. Hypochlorous acid, HOClii. Chlorous acid, HOClO or HClO 2iii. Chloric acid, HClO 3iv. Perchloric acid, HClO 47.9 Oxygen and Compounds of oxygen
7.9.1 Dioxygen
a. Preparation
i. Laboratory methods :- By heating oxygen containing salts such
as chlorates, nitrates and permanganates.
2KClO3(s) (^) MnOHeat
2
2KCl(s) + 3O2(g)
- By thermal decomposition of oxides of
metals.
2Ag 2 O(s) ∆ 4Ag(s) + O2(g)
2HgO(s) ∆ 2Hg(l) + O2(g)
HO S S
OOO OO OOH