Is there any way to get Calcium Hydroxide from Calcium Hypochlorite in a series of reactions? (Wrong answers are not allowed, answer only if you know...)
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Answer:
Calcium hypochlorite is an inorganic compound with formula CaO(Cl)2. It is the main active ingredient of commercial products called bleaching powder, chlorine powder, or chlorinated lime, used for water treatment and as a bleaching agent.[1] This compound is relatively stable and has greater available chlorine than sodium hypochlorite (liquid bleach).[2] It is a white solid, although commercial samples appear yellow. It strongly smells of chlorine, owing to its slow decomposition in moist air. It is not highly soluble in hard water, and is more preferably used in soft to medium-hard water. It has two forms: dry (anhydrous); and hydrated (hydrous).
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Answer:
Calcium hypochlorite is an inorganic compound with formula CaO(Cl)2. It is the main active ingredient of commercial products called bleaching powder, chlorine powder, or chlorinated lime, used for water treatment and as a bleaching agent.[1] This compound is relatively stable and has greater available chlorine than sodium hypochlorite (liquid bleach).[2] It is a white solid, although commercial samples appear yellow. It strongly smells of chlorine, owing to its slow decomposition in moist air. It is not highly soluble in hard water, and is more preferably used in soft to medium-hard water. It has two forms: dry (anhydrous); and hydrated.
Calcium Hypochlorite
Calcium hypochlorite, Ca(OCl)2, an inexpensive and easily stored oxidant, can be used to cleave α-glycols to the corresponding carbonyl compounds.α-Diones, α-hydroxy ketones and α-hydroxy and α-keto acids are also oxidatively fragmented.19 Aldehydic products are further oxidized to acids with an excess of the reagent. Consequently, this reaction is more suitable to produce carboxylic acids from 1,2-diols on a preparative scale.α,β-Unsaturated aldehydes and aromatic aldehydes with electron-donating groups undergo a competing nuclear chlorination, whereas aliphatic aldehydes and aromatic aldehydes with electron-withdrawing groups give the expected acids.20 Reactions are carried out at room temperature in aqueous acetonitrile/acetic acid solution.