KnowraSulfuric acidLinked fromLinked fromThe 53 pages that link to Sulfuric acid, each with the reason it gives.All 53Broader topic 7Related 25Narrower topic 1Compared with 20Hydrochloric acidCompared with: It is another major industrial mineral acid, but can donate two protons and has distinct dehydrating properties.Nitric acidCompared with: It is another major industrial acid, with different acid-base and dehydrating properties.Perchloric acidCompared with: Both are strong mineral acids, but sulfuric acid donates two protons and has different hazards.Hydrofluoric acidCompared with: It causes severe corrosive burns but does not share hydrofluoric acid’s systemic fluoride effects.Sulfonic acidCompared with: Replacing one hydroxyl hydrogen with an organic group distinguishes sulfonic acids from sulfuric acid.Sulfurous acidCompared with: Its stable, isolable acid contrasts with the conventional and unstable sulfurous-acid representation.Antimony pentafluorideCompared with: Ordinary strong aqueous acids contrast with SbF₅-based superacid systems, which can protonate far weaker bases.Chloric acidCompared with: It contrasts chloric acid’s monoprotic formula with a widely used polyprotic oxoacid.Fluoroantimonic acidCompared with: It is the conventional benchmark that superacids are defined as stronger than.Fluorosulfuric acidCompared with: Replacing one hydroxyl group of sulfuric acid with fluorine gives fluorosulfuric acid.Magic acidCompared with: It provides the familiar reference point exceeded by superacids such as magic acid.Phosphorus oxyacidsCompared with: Its proton-transfer behavior contrasts with the generally weaker, often polyprotic phosphorus oxyacids.Trichloroacetic acidCompared with: It illustrates a powerful inorganic acid used in analysis, unlike this chlorinated organic acid.Carborane acidCompared with: It anchors the conventional superacid definition that carborane acids greatly exceed.Triflic acidCompared with: Triflic acid can be stronger while avoiding sulfuric acid’s characteristic dehydrating behavior.Thiosulfuric acidCompared with: Replacing one of its oxygen atoms with sulfur gives the structural relationship used to define thiosulfuric acid.Chlorosulfuric acidCompared with: Replacing one hydroxyl group of sulfuric acid with chlorine gives chlorosulfuric acid.Peroxymonosulfuric acidCompared with: Replacing one sulfuric-acid oxygen with a peroxide group gives Caro’s acid.Selenic acidCompared with: It is the closest common structural analogue, but differs in oxidizing behavior and stability.Solid acidCompared with: It is a familiar liquid-acid catalyst whose corrosiveness and separation differ from solid-acid use.
KnowraSulfuric acidLinked fromLinked fromThe 53 pages that link to Sulfuric acid, each with the reason it gives.All 53Broader topic 7Related 25Narrower topic 1Compared with 20Hydrochloric acidCompared with: It is another major industrial mineral acid, but can donate two protons and has distinct dehydrating properties.Nitric acidCompared with: It is another major industrial acid, with different acid-base and dehydrating properties.Perchloric acidCompared with: Both are strong mineral acids, but sulfuric acid donates two protons and has different hazards.Hydrofluoric acidCompared with: It causes severe corrosive burns but does not share hydrofluoric acid’s systemic fluoride effects.Sulfonic acidCompared with: Replacing one hydroxyl hydrogen with an organic group distinguishes sulfonic acids from sulfuric acid.Sulfurous acidCompared with: Its stable, isolable acid contrasts with the conventional and unstable sulfurous-acid representation.Antimony pentafluorideCompared with: Ordinary strong aqueous acids contrast with SbF₅-based superacid systems, which can protonate far weaker bases.Chloric acidCompared with: It contrasts chloric acid’s monoprotic formula with a widely used polyprotic oxoacid.Fluoroantimonic acidCompared with: It is the conventional benchmark that superacids are defined as stronger than.Fluorosulfuric acidCompared with: Replacing one hydroxyl group of sulfuric acid with fluorine gives fluorosulfuric acid.Magic acidCompared with: It provides the familiar reference point exceeded by superacids such as magic acid.Phosphorus oxyacidsCompared with: Its proton-transfer behavior contrasts with the generally weaker, often polyprotic phosphorus oxyacids.Trichloroacetic acidCompared with: It illustrates a powerful inorganic acid used in analysis, unlike this chlorinated organic acid.Carborane acidCompared with: It anchors the conventional superacid definition that carborane acids greatly exceed.Triflic acidCompared with: Triflic acid can be stronger while avoiding sulfuric acid’s characteristic dehydrating behavior.Thiosulfuric acidCompared with: Replacing one of its oxygen atoms with sulfur gives the structural relationship used to define thiosulfuric acid.Chlorosulfuric acidCompared with: Replacing one hydroxyl group of sulfuric acid with chlorine gives chlorosulfuric acid.Peroxymonosulfuric acidCompared with: Replacing one sulfuric-acid oxygen with a peroxide group gives Caro’s acid.Selenic acidCompared with: It is the closest common structural analogue, but differs in oxidizing behavior and stability.Solid acidCompared with: It is a familiar liquid-acid catalyst whose corrosiveness and separation differ from solid-acid use.