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nalin [4]
3 years ago
6

Is anyone else's brainly not working or is mine the only one that is tweaking?

Chemistry
1 answer:
omeli [17]3 years ago
5 0
Mine tweaking as well
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Lithium diisopropylamide (LDA) is used as a strong base in organic synthesis. LDA is itself prepared by an acid-base reaction be
kakasveta [241]

Explanation:

Lithium diisopropylamide (LDA) is used in many organic synthesis and is a strong base. It is prepared by the acid base reaction of N,N-diisopropylamine ( [(CH₃)₂CH]₂NH ) and butyllithium ( Li⁺⁻CH₂CH₂CH₂CH₃ ).

The equation is show below as:

[(CH₃)₂CH]₂NH + Li⁺⁻CH₂CH₂CH₂CH₃  ⇒  [(CH₃)₂CH]₂N⁻Li⁺  + CH₃CH₂CH₂CH₃

N,N-diisopropylamine ( [(CH₃)₂CH]₂NH ) is a weaker acid and hence,  LDA ( [(CH₃)₂CH]₂N⁻Li⁺ ) is stronger base. (Weaker acid has stronger conjugate base)

Butyllithium ( Li⁺⁻CH₂CH₂CH₂CH₃ ) is a very strong base and hence, butane ( CH₃CH₂CH₂CH₃ ) is a very weak acid. (Strong base has weaker conjugate acid)

5 0
3 years ago
When NH4NO3­ spontaneously dissolves in water the temperature of the solution decreases. What factors make this a naturally occu
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Explanation:

Once solid ammonium nitrate interacts with water, the molecules of polar water intermingle with these ions and attract individual ions from the structure of the lattice, that actually will break down. E.g;-NH4NO3(s) — NH4+(aq)+ NO3-(aq) To split the ionic bonds that bind the lattice intact takes energy that is drained from the surroundings to cool the solution.

Some heat energy is produced once the ammonium and nitrate ions react with the water molecules (exothermic reaction), however this heat is far below that is needed by the H2O molecules to split the powerful ionic bonds in the solid ammonium nitrate.

Hence, we can say that the dissolution of ammonium nitrate in water is highly endothermic reaction.

8 0
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