- the
inorganic compound with the
formula HSO3Cl. It is also
known as
chlorosulfonic acid,
being the
sulfonic acid of chlorine. It is a distillable, colorless...
- with a
smoke generating mixture such as
sulfur trioxide dissolved in
chlorosulfonic acid.
These so-called "smoke bottles" do not need a
source for ignition...
- the
first stage of synthesis, it
undergoes sulfonylchlorination by
chlorosulfonic acid,
forming 4-chloro-3-chlorosulfonylbenzoic acid,
which is further...
- organosulfates. It is more
expensive than
other reagents for
doing this, such as
chlorosulfonic acid or oleum, but is also
significantly milder and will not sulfonate...
-
methyl chlorosulfonate (CH3ClO3S)
called "C-stoff" in Germany, or with
chlorosulfonic acid
called "Rationite" in France. The
esterification of
sulfuric acid...
- (36,450 ft)
Smoke FS M60 S**** 20.09 kg (44 lb)
Sulfur trioxide in
chlorosulfonic acid, 2.09 kg (5 lb)
Chemical H M60 S**** 19.43 kg (43 lb)
Mustard gas...
-
another route begins with o-chlorotoluene.
Sulfonation of
toluene by
chlorosulfonic acid
gives the
ortho and para
substituted sulfonyl chlorides. The ortho...
-
which can be a
problem with
sulfuric acid,
fluorosulfuric acid, and
chlorosulfonic acid.
Below is a
prototypical sulfonation,
which triflic acid does not...
- acid then
restores the
original aldehyde or ketone. NH2OH
reacts with
chlorosulfonic acid to give hydroxylamine-O-sulfonic acid: HO−S(=O)2−Cl + NH2OH → NH2−O−S(=O)2−OH...
- (853 m/s) 25,940 yds (23,720 m)
Smoke FS M104 S****
Sulfur trioxide in
chlorosulfonic acid 2800 ft/s (853 m/s) 25,940 yds (23,720 m)
Chemical H M104 S****...
