Sodium Metal when treated with ethyne forms mono and di sodiumethynide why doesn't lithium ?
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1$\begingroup$ Related: Why are lithides not known? $\endgroup$– andselisk ♦Aug 5, 2017 at 17:47
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1$\begingroup$ @andselisk I'm not asking about lithides. In mono sodium ethynide sodium has a positive charge $\endgroup$– SerotoninAug 6, 2017 at 3:46
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$\begingroup$ It looks like it does form monolithium ethynide, which should also react to form dilithium ethynide. onlinelibrary.wiley.com/doi/10.1002/047084289X.rl035.pub2/… $\endgroup$– Tyberius ♦Aug 6, 2017 at 3:58
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$\begingroup$ @Tyberius Yep! You're right en.m.wikipedia.org/wiki/Acetylide anyways I asked because my school textbook was saying lithium does not form Acetylide $\endgroup$– SerotoninAug 6, 2017 at 4:10
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$\begingroup$ @NilayGhosh Thanks for the explanation. But why lithium doesn't reacts directly with terminal alkynes ? $\endgroup$– SerotoninAug 12, 2017 at 1:50
2 Answers
Sodium alkynide was formed by reacting sodium and acetylene but in case of lithium alkynide, it can be formed by reacting acetylene with organolithium reagents like BuLi, Lithium amide, LiHMDS. From wikipedia:
Lithium amide, LiHMDS, or organolithium reagents, such as butyllithium, are frequently used form lithium acetylides:
$\ce{H-C#C-H + BuLi ->[THF][-78℃] Li -#-H + BuH}$
The above process is well described in this paper which @Tyberius linked in the comment section.
Lithium actually can be reacted with acetylene to produce the ethynide:
In the laboratory samples may be prepared by treating acetylene with a solution of lithium in ammonia, on −40°C, with creation of addition compound of $\ce{Li2C2 • C2H2 • 2NH3}$ that decomposes in stream of hydrogen at room temperature giving white powder of $\ce{Li2C2}$.
$\ce{C2H2 + 2Li -> Li2C2 + H2}$
However,
Samples prepared in this manner generally are poorly crystalline.
Various alternatives are therefore often preferred, and (some of) these are also given in the Wikipedia article, and by Nilay Ghosh in his answer.