Search results
Results from the WOW.Com Content Network
Sodium aluminate is an inorganic chemical that is used as an effective source of aluminium hydroxide for many industrial and technical applications. Pure sodium aluminate is a white crystalline solid having a formula variously given as NaAlO 2, NaAl(OH) 4 (), [3] Na 2 O·Al 2 O 3, or Na 2 Al 2 O 4.
In this reaction, sodium hydroxide acts as an agent to make the solution alkaline, which aluminium can dissolve in. 2 Al + 2 NaOH + 2 H 2 O → 2 NaAlO 2 + 3 H 2 Sodium aluminate is an inorganic chemical that is used as an effective source of aluminium hydroxide for many industrial and technical applications.
Similarly to the nucleophilic carbon center in the carbene, the lone pair on the aluminium center binds to the first azide equivalent. Nitrogen gas is liberated. With the second equivalent of azide, a five-member ring is formed. Aluminium (I) systems undergo reactions with azides in the same fashion as carbenes. [10]
Aluminium oxide is an amphoteric substance, meaning it can react with both acids and bases, such as hydrofluoric acid and sodium hydroxide, acting as an acid with a base and a base with an acid, neutralising the other and producing a salt. Al 2 O 3 + 6 HF → 2 AlF 3 + 3 H 2 O Al 2 O 3 + 2 NaOH + 3 H 2 O → 2 NaAl(OH) 4 (sodium aluminate)
Aluminium has a high chemical affinity to oxygen, which renders it suitable for use as a reducing agent in the thermite reaction. A fine powder of aluminium reacts explosively on contact with liquid oxygen; under normal conditions, however, aluminium forms a thin oxide layer that protects the metal from further corrosion by oxygen, water, or ...
The reduction of nitro compounds are chemical reactions of wide interest in organic chemistry. The conversion can be effected by many reagents. The nitro group was one of the first functional groups to be reduced. Alkyl and aryl nitro compounds behave differently.
Sodium aluminium hydride is a strong reducing agent, very similar in reactivity to lithium aluminium hydride (LAH) and, to some extent, Diisobutylaluminium hydride (DIBAL) in organic reactions. [6] It is much more powerful reducing agent than sodium borohydride due to the weaker and more polar Al-H bond compared to the B-H bond.
Aluminium hydride reduces acetals to half protected diols. [1] Acetal reduction using aluminium hydride. Aluminium hydride reduces epoxide to the corresponding alcohol: [1] Epoxide reduction using aluminium hydride. The allylic rearrangement reaction carried out using aluminium hydride is a S N 2 reaction, and it is not sterically demanding: [1]