Noun:

ఆర్సెనిక్ ఆమ్లం,

arsenic acid తెలుగు అర్థానికి ఉదాహరణ:

ఆర్సెనిక్ గాఢ నత్రికామ్లంతో చర్య వలన ఆర్సెనిక్ ఆమ్లం, సజల నత్రికామ్లంతో చర్య వలన అర్సేనియాస్ ఆమ్లంఏర్పడును.

arsenic acid's Usage Examples:

The reaction is an electrophilic aromatic substitution, using arsenic acid as the electrophile.

Arsenates are salts or esters of arsenic acid (H3AsO4), consisting of the ion AsO43−.

He conducted experiments with arsenic acid as a discharge agent and filed patents for the employment of arsenic.

The first reported synthetic application dates back to 1868 with Julius Löwe and the synthesis of ellagic acid by heating gallic acid with arsenic acid or silver oxide.

Scheele prepared a number of arsenates by the action of arsenic acid on the alkalies.

The process involves the reaction of aniline and arsenic acid via an electrophilic aromatic substitution reaction.

The compound can be obtained by neutralizing arsenic acid: H3AsO4 + 3 NaOH → Na3AsO4 + 3 H2O The salt (as its dodecahydrate) is.

Arsanilic acid, also known as aminophenyl arsenic acid or aminophenyl arsonic acid, is an organoarsenic compound, an amino derivative of phenylarsonic.

Also biologist, physician, and pharmacist, Béchamp reported it 40 to 50 times less toxic as a drug than arsenic acid, and named it Atoxyl, the first organic arsenical drug.

equilibria for aqueous solutions of this diprotic acid derived from arsenic acid are as follows: H3AsO4 + H2O ⇌ H 2AsO− 4 + H3O+  (pKa1 2.

This colourless solid is an organic derivative of arsenic acid, AsO(OH)3, where one OH group has been replaced by a phenyl group.

iron(III) sulfate and sulfuric acid, and in the case of arsenopyrite, arsenic acid is also produced.

In Germany, Paul Ehrlich inferred Béchamp's report of Atoxyl's structure incorrect, and Ehrlich with his chief organic chemist Alfred Bertheim found its correct structure—aminophenyl arsenic acid or aminophenyl arsonic acid—which suggested possible derivatives.

Synonyms:

acid,

Antonyms:

pleasant, sweet,