|
element |
required compound |
link to experiment |
* |
Cl |
Al (foil)
NaCl
CuSO4·5H2O
HCl (10%) |
Influence of combination of copper ions and
chloride ions on reactivity of aluminium. A violent reaction only
occurs, when both type of ions are present. |
* |
Cl, I, Br |
Bi(NO3)3·xH2O
HNO3
(dilute)
HCl
(dilute)
NaCl
KBr
KI |
Bismuth complexes with halogens.
Bismuth in its +3 oxidation state forms a black precipitate with iodide
ions, and a deep orange complex is formed when excess iodide ion is
present. Chloride and bromide also form complexes. |
* |
Br |
KBr
K2Cr2O7
(or subst.) |
Synthesis of potassium bromate. It
is shown how potassium bromate can be made by means of electrolysis. |
* |
Br |
NaBr
NaHSO4
(pH-minus)
Any soluble hexavalent chromium compound |
Bromine from OTC compounds. Bromine
is prepared from standard swimming pool chemicals. Only a very small
amount of chromate or dichromate is needed, but this can be made easily
as well (no need to isolate and purify this). |
* |
Br |
Br2
Al (foil)
HCl (10%)
Na2SO3 |
Reaction between bromine and aluminium,
spontaneous ignition of aluminium after some delay
. Aluminium foil
is added to some liquid bromine. |
* |
Br |
Br2-water
NH3
(10%) |
Formation of dense smoke from bromine and
ammonia
. Bromine vapor is
poured into air, containing ammonia gas. |
* |
Br, Cl |
Br2
Cl2 P (red)
|
Reaction between bromine/chlorine and
phosphorus .
Red phosphorus, when thrown in chlorine gas or bromine vapor, is ignited
and continues burning in the gas. |
* |
Br, I |
NaBrO3
NH4NO3
HIO3
NH3 (12% or better) |
Ammonium halates, unstable
compounds .
Ammonium bromate and ammonium iodate are prepared and it is demonstrated
how easily and violently they decompose on slight heating. This is a
nice and fairly spectacular experiment, but it should not be scaled up. |
* |
Br, P |
P (red)
Br2
|
Synthesis and isolation of phosphorus
tribromide .
Phosphorus tribromide is prepared by means of careful addition of red
phosphorus to bromine. By means of distillation the product is purified. |
* |
Br, N |
NaBrO3
KBr (or NaBr)
NH2OH·HCl
H2SO4 (dilute)
|
Spectacular violent reaction with time
delay .
Hydroxylamine and bromate react violently (explosively), but not immediately after
mixing. For tens of seconds nothing seems to happen and then suddenly the mix
reacts extremely violently. This is a very interesting phenomenon, and it is
possible to explain this behavior quite well, using a simple model. |
* |
Cl |
KCl
CsCl
(optional)
K2Cr2O7
(optional)
HCl
(dilute, optional) |
Tutorial for making a
miniature electrolysis cell for chlorate production. This is not
really an experiment, it is a description of how one can setup a nice
small electrolysis cell, suitable for making chlorates from chlorides.
The good working of this cell is demonstrated for making potassium
chlorate and cesium chlorate. |
* |
Cl |
NaClO3
HCl (30%)
Ca(ClO)2·xH2O |
Colored gases - chlorine and chlorine dioxide
. Chlorine gas and
chlorine dioxide are made. A comparison is made of the intensity of
their colors. |
* |
Cl |
NaClO2
HCl (30%)
|
Explosive properties of chlorine
dioxide
. The brightly
colored chlorine dioxide gas is prepared and ignited. This results in a
nice and quite spectacular decompositon reaction. |
* |
Cl |
NaClO2
HCl (≥
25%)
NH3
(5%)
|
Explosion of chlorine dioxide, initiated
by presence of ammonia
. Another
experiment, which demonstrates the danger of chlorine dioxide. This
experiment shows how chlorine dioxide can be brought to explosion,
simply by adding a few drops of household ammonia. |
|
Cl |
NH3 (5%)
CuSO4·5H2O
organic swimming pool chlorine |
Funny experiments with organic
swimming pool chlorine. Several funny experiments with TCCA. Smoke
production, formation of strange precipitates. |
* |
Cl |
H2O2
(30%)
swimming
pool tablets |
Red chemiluminiscence with chlorine
swimming pool chemicals. Hydrogen peroxide is added to sodium
dichloro isocyanurate or to calcium hypochlorite. A nice red
chemiliminiscent light is produced. |
|
Cl, Br, I |
Cl2
Br2
I2 |
Colored gases from halogens.
Halogens are mixed, and the interhalogen compounds formed are shown in
their vapor state. |
* |
Cl |
Cl2
CaC2
("carbide") |
Violent 'combustion' of acetylene in
chlorine gas, explosions without need of supplying heat
. Acetylene gas is
bubbled into chlorine and this leads to violent explosions. |
* |
Cl |
any
soluble Mn salt
any
soluble Fe salt
bleach |
Oxidizing power of bleach, bringing iron and
manganese to highest oxidation state. Simple household bleach is
capable of oxidizing iron to its +6 oxidation state and manganese to its
+7 oxidation state. |
* |
Cl, P |
P (white)
NaOH
Cl2
bleach
HCl |
Self-ignition of
phosphine in chlorine gas .
In this experiment some phosphine is prepared, and the gas is bubbled in
an atmosphere of chlorine, resulting in self-ignition of the gas and
contraction of gas volume. This demonstrates the high reactivity of
chlorine. |
* |
Cl, P,
Al |
P (red)
Cl2
KNO3
Al
(powder) |
Miniature fireworks (bright flashes)
in a test tube. A mix of aluminium powder, potassium nitrate and red
phosphorus is thrown in chlorine gas. This results in a very bright
white flash. |
* |
Cl, N |
N2H4
(dilute, 20%)
HClO4
(dilute, 20%) |
Violent decomposition of
hydrazine perchlorate and fairy-like sparkles. A small quantity of
hydrazine perchlorate is prepared and this compound is heated, leading
to a peculiar fairy-like sparkling when heating is not too strong and
violent deflagration on stronger heating. |
* |
Cl, Br, I, N |
N2H4.2HCl
Ca(OCl)2
NaClO2
KClO3
KBrO3
KIO3
KIO4
|
Reactivity of different
oxohalogenate ions.
Several oxohalogenate compounds are added to a concentrated solution of
hydrazine dihydrochloride. In many cases this leads to a reaction, some
of them being very violent. A comparison is made of the reactivity of
the different oxohalogenate ions at room temperature. |
* |
Cl, Br, I,
Te |
TeO2
Na2TeO3
HCl (30%
by weight)
HBr (40%
by weight)
H2SO4
(dilute)
KI
Na2SO3 |
Colorful properties of halogen
complexes of tellurium in oxidation state +4.
At very low pH, tellurium in oxidation state +4 forms remarkable
compounds with the halide ions. The heavier the halogen, the more stable
the complex and the more intense the color. All of these complexes,
however, are very prone to hydrolysis in aqueous solution. |
* |
F |
KMnO4
NaF
H2SO4
(concentrated)
Na2S2O5
(or Na2SO3) |
A volatile compound of manganese
and corrosion of glass
. A volatile green
compound of manganese(VII) is produced from potassium permanganate,
sodium fluoride and conc. sulphuric acid. |
|
I |
KIO4
S |
Pyrotechnic mix with purple
gaseous combustion product. Potassium periodate, mixed with sulphur
gives a mix, which burns without smoke, but produces a nice purple gas
mix of iodine and sulphur dioxide. |
|
I |
NaIO4
many metal salts |
Colorful
precipitates with periodate ion. Many metal salts are mixed with a
solution of sodium metaperiodate. |
* |
I |
CHI3
Na2SO3
CH3COCH3 |
Decomposition of iodoform. Iodoform is
heated and its decomposition products are shown. |
* |
I, Cl |
KIO3
HCl (30%)
CH3COCH3
H2SO4
H2O2
(3%)
Na2SO3 |
Preparation of polyhalide salt of
potassium. Potassium iodate is added to concentrated hydrochloric
acid. Chlorine gas is formed, and needle-like crystals of potassium
tetrachloroiodate(III) are formed as well. This is a remarkable
polyhalide compound. |
* |
I, Cl |
Rb2CO3
HIO3
HCl (30%) |
A polyhalide compound of
rubidium. Rubidium is known to form polyhalide compounds fairly
easily, more so than the lighter alkali metals (see experiment above).
In this experiment such a compound is prepared. During the preparation a
beautiful crystalline precipitate is formed. |
* |
I, Cl |
I2
Ca(ClO)2·xH2O
Mg
HCl
(dilute)
Na2SO3 |
Example of interhalogen compounds
. Chlorine gas is
made, and this gas is lead over iodine. Iodine monochloride and iodine
trichloride are formed. The monochloride is reacted with magnesium. |
* |
I |
KIO3
KH(IO3)2
NaNO2 |
Reaction between molten nitrite
and iodate, formation of beautiful wine red gas mixes. |
* |
I |
KIO4
NH4SCN |
Colored smoke -- purple and yellow.
A mix of potassium periodate and ammonium thiocyanate is ignited. This
gives purple smoke, which quickly turns yellow. Quite a remarkable
experiment. |
* |
I |
H5IO6
NH3
NaOH |
Preparation
and properties of ammonium periodate. A simple experiment, in which
ammonium (meta)periodate is made. This compound explodes when it is
heated. |
* |
I, Mg |
Mg
(powder)
I2
Na2SO3 |
Water-initiated violent reaction between
magnesium and iodine. Magnesium and iodine are mixed, and a violent
reaction is initiated by adding some water. |
* |
I, N |
H5IO6
N2H4
alternatives based on KIO4 and
salts of hydrazine are possible |
Violent
reaction between hydrazine and periodate. In this experiment it is
demonstrated that hydrazine and periodate react extremely violently and
so much heat is produced that iodine escapes as vapor, even from aqueous
solutions! |
* |
I |
KIO3
KOH
Cl2 (generated)
HNO3 |
Synthesis of
potassium periodate. Potassium periodate is prepared by leading
chlorine gas through a solution of potassium iodate and potassium
hydroxide. Some acid is used to precipitate all of the periodate as the
very sparingly metaperiodate. |
* |
I |
NaI
NaOH
Cl2 (generated) |
Synthesis of sodium
orthoperiodate. Sodium orthoperiodate is prepared by leading
chlorine gas through a solution of sodium iodide and sodium
hydroxide. The nice thing of this synthesis is that it allows one to
make periodate without needing access to any special chemicals besides
the easy to obtain sodium iodide. |
* |
I, P |
H5IO6
P (red) |
Delayed self-ignition of
mix of periodic acid and red phosphorus. Some red phosphorus and
periodic acid are mixed. After a while, this mix suddenly self-ignites
and a plume of fire and smoke is produced. |
* |
I |
I2
oleum (20%
SO3)
|
Formation of
cationic iodine species in oleum. Iodine is dissolved in oleum and
the formation of a blue cationic species is demonstrated. Iodine is
brought to oxidation state +½, which is very special for iodine. |
* |
I, Sn |
Sn
(preferably powder)
I2
CH2Cl2
or CS2 |
Preparation of tin(IV) iodide, a volatile
covalent compound. Tin and iodine are made to react in a suitable
solvent for iodine. Under these conditions the interesting compound
tin(IV) iodide is formed, which can easily be isolated. Some properties
of this compound are shown. |
|
technical |
NaBr
KBrO3
H2SO4
(concentrated) |
Making bromine by
distillation. Bromine is made in an acidic solution and this is
distilled in order to obtain the pure element. It is dried with
concentrated sulphuric acid. |