Properties of H2 (Dihydrogen)
Properties of H2 (Dihydrogen)
Dihydrogen is
a colorless, odorless, tasteless, combustible gas. It is lighter than air and
insoluble in water.
Chemical properties
The chemical
behavior of dihydrogen is determined, to a large extent, by bond dissociation
enthalpy. The H-H bond dissociation enthalpy is the highest for a single bond
between two atoms of any element. What inferences would you draw from this fact?
It is because of this factor that the dissociation of dihydrogen into its atoms
is only 0.081% around 200K which increases to 95.5% at 500K. Also, it is
relatively inert at room temperature due to the high H-H bond enthalpy. Thus,
the atomic hydrogen is produced at a high temperature in an electric arc or
under ultraviolet radiations. Since its orbital is incomplete with 1s1
electronic configuration, it does combine with almost all the elements. It accomplishes
reactions by (i) loss of the only electron to give H+, (ii) gain of
an electron to form H- , and (iii) sharing electrons to form a
single covalent bond.
The chemistry
of dihydrogen can be illustrated by the following reactions:
Reaction with halogens: It reacts with halogens, X2
to give hydrogen halides, HX,
H2
(g) +
X2 (g) → 2HX (g)
(X= F, Cl, Br, I)
While the
reaction with fluorine occurs even in the dark, with iodine it requires a catalyst.
Reaction with dinitrogen: with dinitrogen it forms ammonia.
Reactions with metals: With many metals it combines at
high a temperature to yield the corresponding hydrides.
H2
(g) + 2M (g) → 2MH(s); where M is an alkali meal.
Reaction with metal
ions and metal oxides: It reduces some metal ions in aqueous solution and oxides of metals
(less active than iron) into corresponding metals.
H2
(g) + Pd2+ (aq) → Pd(s) + 2H+ (aq)
yH2
(g) + MxOy (s) → xM(s) + yH2O
(1)
Reaction with organic
compounds : It
reacts with many organic compounds in the presence of catalysts to give useful
hydrogenated products of commercial importance. For example:
- Hydrogenation of vegetable oils using nickel as catalyst gives edible fat (margarine and vanaspati ghee)
- Hydroformylation of olefins yields aldehydes which further undergo reduction to give alcohols.
H2 +
CO + RCH
= CH2 → RCH2CH2CHO
H2 + RCH2CH2CHO → RCH2CH2CH2OH
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