Question

Reaction not involving a carbanion is (a) Aldol condensation (b) Claisen condensation (c) Pinacol pinacolone rearrangement (d) Michael reaction

Short answer

Pinacol-Pinacolone rearrangement does not involve a carbanion.

Step-by-step solution

Understand Carbanions

A carbanion is a negatively charged carbon atom, often formed during organic reactions where the carbon atom is bonded to an electron-withdrawing group. Carbanions act as nucleophiles in reactions.

Analyze Aldol Condensation

In Aldol condensation, an enolate ion (a type of carbanion) reacts with a carbonyl compound to form a β-hydroxy aldehyde or ketone, which may dehydrate to give a conjugated enone. This reaction involves the formation of a carbanion intermediate.

Analyze Claisen Condensation

Claisen condensation involves two esters or one ester and one ketone reacting in the presence of a strong base to form a β-keto ester or β-diketone. An enolate ion, which is a carbanion species, acts as a nucleophile in this reaction.

Analyze Pinacol-Pinacolone Rearrangement

The Pinacol-Pinacolone rearrangement involves the conversion of a glycol (a diol) into a ketone under acidic conditions, typically not involving a carbanion. The mechanism involves carbocations and rearrangement, avoiding carbanion involvement.

Analyze Michael Reaction

In the Michael reaction, a carbanion (or nucleophile) adds to an α,β-unsaturated carbonyl compound. This process clearly involves the formation and participation of a carbanion as the nucleophile.

Identify Reaction Not Involving Carbanion

Based on the analyses, the Pinacol-Pinacolone rearrangement stands out as the reaction that does not involve a carbanion. It utilizes a carbocation mechanism instead.

Key concepts

Carbanion

A carbanion is an important species in organic chemistry that plays a pivotal role in many reactions. It is formed when a carbon atom gains an extra electron, resulting in a negatively charged ion. This occurs often when carbon is attached to atoms or groups that pull away electrons, known as electron-withdrawing groups.
Carbanions are characterized by their nucleophilic nature, meaning they have a tendency to donate electrons to positively charged atoms or regions in other molecules. High electron density at the carbanion center makes it strongly reactive with electrophiles, which are electron-deficient species. This property makes carbanions versatile intermediates in various organic synthesis processes.
To stabilize a carbanion, factors like resonance and inductive effects are essential. For example, neighboring carbonyl groups can stabilize a carbanion through resonance, spreading the negative charge to oxygen. Understanding these stabilization factors helps predict and control carbanion behaviors in reactions.

Aldol Condensation

Aldol condensation is a reaction where an enolate ion, which forms from a carbonyl compound, acts as a carbanion to initiate the process by attacking another carbonyl group's carbon atom. This is how a new carbon-carbon bond is formed.
In the reaction, a β-hydroxy aldehyde or ketone is typically produced. This intermediate can further dehydrate to form a conjugated enone, a compound with a double bond next to a carbonyl group. The dehydration is usually promoted by heating or acidic conditions.
Aldol condensation is valuable in organic synthesis as it allows the formation of complex molecules from simpler ones. The reaction exploits the nucleophilic character of the enolate ion formed from a carbonyl compound, emphasizing the role of carbanions in forming new molecular structures.

Claisen Condensation

Claisen condensation resembles aldol condensation but involves esters. Here, a strong base induces the formation of an enolate ion from an ester, which then acts as a carbanion. This nucleophile attacks the carbonyl carbon of another ester or a ketone, facilitating the formation of a new carbon-carbon bond.
The product of Claisen condensation is typically a β-keto ester or a β-diketone, depending on the reagents used. This reaction solidifies the relationship between carbanions and enolate ions, showing how these species mediate important transformations in organic chemistry.
Applications of Claisen condensation are widespread in the synthesis of natural products and complex organic molecules, making it a cornerstone reaction for chemists exploring carbon-carbon bond formation.

Michael Reaction

The Michael reaction is a classic example of a conjugate addition where a carbanion adds to an α,β-unsaturated carbonyl compound, forming a substantial new carbon-carbon bond.
In this reaction, the carbanion is typically derived from a compound known as a "Michael donor," which often contains a stabilized carbanion. This donor is paired with a "Michael acceptor," generally an unsaturated carbonyl compound, to complete the reaction.
Michael reactions are crucial in the construction of complex organic molecules, especially those that require multiple chiral centers. Its versatility and reliability make it a preferred method for forming lengthy carbon chains and rings, contributing significantly to organic synthesis and industry applications.