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The creation of enolate ions:
The first thing you will learn is that a specific group of carbonyl compounds with the name of C=O reacts very easily when coming into contacts with both nucleophiles and electrophiles. This C=O is also very reactive toward Hs and as a result an acidic solution is created. That is called enolate ions. These ions are reactive toward nucleophiles and electrophiles in a different way. You will get to understand from Reactions using Enolate Ions Assignment Help that carbonyl compounds that are recognized as a-CHs are found to isomerize enols.
Different types of reactions:
Those enolate ions are very reactive toward various components. But you will get to concentrate on three major reactive substrates when understanding this matter. You will learn from Reactions using Enolate Ions Homework Help about them as:
When focusing on the first type of reactions then ions are prone to replace H in the solution of a-C-H. This process is called a-halogenation. In the second type of reaction, alkyl group R` replaces H from the solution called a-C-H andthis process is called a-alkylation. In the third reaction, nucleophilic a-C is added in the C=O that are found in various types of carbonyle compounds.
In this context, you will find from Reactions using Enolate Ions Assignment Help that,
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