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Lithium imide is an inorganic compound with the chemical formula Li 2 N H. This white solid can be formed by a reaction between lithium amide and lithium hydride. [1] LiNH 2 + LiH → Li 2 NH + H 2. The product is light-sensitive and can undergo disproportionation to lithium amide and characteristically red lithium nitride. 2 Li 2 NH → LiNH 2 ...
Heating lithium amide with lithium hydride yields lithium imide and hydrogen gas. This reaction takes place as released ammonia reacts with lithium hydride. [2] Heating magnesium amide to about 400 °C yields magnesium imide with the loss of ammonia. Magnesium imide itself decomposes if heated between 455 and 490 °C. [6]
Lithium amide or lithium azanide is an inorganic compound with the chemical formula LiNH 2. It is a white solid with a tetragonal crystal structure. [1] Lithium amide can be made by treating lithium metal with liquid ammonia: [2] 2 Li + 2 NH 3 → 2 LiNH 2 + H 2. Lithium amide decomposes into ammonia and lithium imide upon heating. [3]
It is commonly used as Li-ion source in electrolytes for Li-ion batteries as a safer alternative to commonly used lithium hexafluorophosphate. [3] It is made up of one Li cation and a bistriflimide anion.
The result is a condensation reaction: [5] (RCO) 2 O + R′NH 2 → (RCO) 2 NR′ + H 2 O. These reactions proceed via the intermediacy of amides. The intramolecular reaction of a carboxylic acid with an amide is far faster than the intermolecular reaction, which is rarely observed.
Lithium imide can also be formed under certain conditions. Some research has explored this as a possible industrial process to produce ammonia since lithium hydride can be thermally decomposed back to lithium metal. Lithium nitride has been investigated as a storage medium for hydrogen gas, as the reaction is reversible at 270 °C. Up to 11.5% ...
Amide reduction is a reaction in organic synthesis where an amide is reduced to either an amine or an aldehyde functional group. [ 1 ] [ 2 ] Catalytic hydrogenation
An intramolecular S N 2 reaction by the anion forms the cyclic backbone of morphine. [14] Synthesis of morphine using lithium–halogen exchange. Lithium–halogen exchange is a crucial part of Parham cyclization. [15] In this reaction, an aryl halide (usually iodide or bromide) exchanges with organolithium to form a lithiated arene species.