Hydrogen sulfide is a weak acid. It can dissociate in water to produce hydrosulfuric acid, but it does not fully ionize like strong acids such as hydrochloric acid.
acid precipatation
Bromide is not, in an of itself, an acid or a base. Bromide is capable of combining with an H+ ion and then becomes Hydrobromic Acid. Due to Bromine's position on the periodic table it is likely to form acids, not bases.
Hydrofluoric acid is the Arrhenius acid that contains the fluoride anion.
Bromine itself is not considered an acid. However, it can react with water to a small degree to form hydrobromic acid (HBr), a strong acid and hypobromous acid (HBrO) a weak acid. Br2 + H2O --> HBr + HBrO
Sulphanilic acid is acidic due to the presence of a carboxylic acid group (COOH). This group can donate a proton (H+) in a reaction, making sulphanilic acid acidic in nature.
Sulphanilic acid can be prepared from aniline by diazotization with sodium nitrite in acidic conditions to form diazonium salt, followed by heating or treatment with sulfur dioxide gas to convert the diazonium salt to sulphanilic acid.
Methyl Orange is an indicator that is used to indicate the equivilance point of and acid-base titration. In acidic environments, it turns red and in basic environemnts, or pH of 4.4 and higher, it turns yellow. It is prepared by treatment of helianthine with sodium hydroxide , helianthine is obtained by coupling diazotised sulphanilic acid with N,N-dimethylaniline .
The basic principle involved in pauly's test is diazotization. The sulphanilic acid gets diazotised in the presence of sodium nitrite and sodium carbonate with the sample. This test answers for tyrosine, tryptophan and histidine residues. Vino.S Faculty, VIT University, Vellore, Tamilnadu.
Ortho sulfanilic acid is more stable than meta sulfanilic acid because the ortho position allows for greater resonance stabilization of the negative charge on the deprotonated form. In the ortho position, the negative charge can be delocalized over two oxygen atoms, leading to enhanced stability. Conversely, in the meta position, there is no such resonance stabilization, resulting in lower stability.
Hydrochloric acid Sulfuric acid Nitric acid Acetic acid Citric acid Phosphoric acid Lactic acid Hydrofluoric acid Tartaric acid Carbonic acid
Hydrochloric acid Sulfuric acid Nitric acid Acetic acid Citric acid Lactic acid Phosphoric acid Hydrofluoric acid Hydrobromic acid Formic acid Carbonic acid Hydroiodic acid Perchloric acid Tartaric acid Maleic acid Benzoic acid Propionic acid Butyric acid Oxalic acid Boric acid
Sulfuric acid Hydrochloric acid Nitric acid
Strong (mineral) acids are ; Hydrochloric Acid Sulphuric Acid Nitric Acid Weak (carboxylic) acids are Ethanoic Acid Methanoic Acid Propnoic Acid .
Some examples that would be considered an acid: sulfuric acid, nitric acid, hydrofluoric acid, perchloric acid, boric acid, periodic acid, salicilic acid, stearic acid, citric acid, oxalic acid, etc.
Citric acid Lactic acid Acetic acid Malic acid Tartaric acid
sulfuric acid or sulphuric acid