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The formation of cyanohydrin from ketone...

The formation of cyanohydrin from ketone is an example of :

A

Electrophilic addition reaction

B

Electrophilic substitution reaction

C

Nucleophilic substitution reaction

D

Nucleophilic addition reaction

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To determine the type of reaction involved in the formation of cyanohydrin from a ketone, we can follow these steps: ### Step-by-Step Solution: 1. **Identify the Reactants**: - We start with a ketone, which has the general structure R-C(=O)-R', where R and R' are hydrocarbon groups. 2. **Introduce the Nucleophile**: - The nucleophile in this reaction is cyanide ion (CN⁻), which can be derived from hydrogen cyanide (HCN). 3. **Mechanism of Reaction**: - The carbon atom in the carbonyl group (C=O) of the ketone is electrophilic due to the partial positive charge on it (δ+), while the oxygen carries a partial negative charge (δ-). - The cyanide ion (CN⁻) attacks the electrophilic carbon atom of the carbonyl group. 4. **Formation of the Intermediate**: - Upon the attack of CN⁻, the double bond between carbon and oxygen breaks, leading to the formation of a tetrahedral intermediate. 5. **Protonation of the Intermediate**: - The oxygen atom in the intermediate carries a negative charge and can be protonated by a proton (H⁺) from the solution, resulting in the formation of the cyanohydrin. 6. **Final Product**: - The final product of this reaction is a cyanohydrin, which has the structure R-C(OH)(CN)-R'. 7. **Classify the Reaction**: - Since the cyanide ion (nucleophile) adds to the carbonyl carbon without replacing any atom, this reaction is classified as a **nucleophilic addition reaction**. ### Conclusion: The formation of cyanohydrin from a ketone is an example of a **nucleophilic addition reaction**. ---
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