For each solvent, indicate the most likely substitution reaction to take place.
(e)

Verified step by step guidance

1. Analyze the solvent structure provided in the image. The solvent shown is acetic acid (CH₃COOH), which is a polar protic solvent due to the presence of a hydroxyl (-OH) group capable of hydrogen bonding.
2. Understand the role of polar protic solvents in substitution reactions. Polar protic solvents stabilize carbocations and nucleophiles through hydrogen bonding, favoring SN1 (unimolecular nucleophilic substitution) reactions.
3. Consider the mechanism of SN1 reactions. These reactions proceed via a two-step mechanism: (1) formation of a carbocation intermediate after the leaving group departs, and (2) nucleophilic attack on the carbocation.
4. Evaluate the likelihood of SN2 (bimolecular nucleophilic substitution) reactions in polar protic solvents. SN2 reactions are less favored in such solvents because the nucleophile is hindered by solvation, reducing its reactivity.
5. Conclude that the most likely substitution reaction to take place in acetic acid as a solvent is an SN1 reaction, given its polar protic nature and ability to stabilize intermediates.

Key Concepts

Nucleophilic Substitution Reactions

Nucleophilic substitution reactions involve the replacement of a leaving group in a molecule by a nucleophile. These reactions can occur via two main mechanisms: SN1, which is a two-step process involving carbocation formation, and SN2, which is a one-step process where the nucleophile attacks the substrate simultaneously as the leaving group departs. The choice of mechanism often depends on the structure of the substrate and the nature of the nucleophile.

Solvent Effects on Reaction Mechanisms

The choice of solvent can significantly influence the rate and mechanism of nucleophilic substitution reactions. Polar protic solvents stabilize ions and favor SN1 mechanisms by stabilizing the carbocation intermediate, while polar aprotic solvents enhance the nucleophilicity of the nucleophile and favor SN2 mechanisms. Understanding solvent effects is crucial for predicting the outcome of substitution reactions.

Leaving Group Ability

The ability of a leaving group to depart from a substrate is a critical factor in nucleophilic substitution reactions. Good leaving groups, such as halides or tosylates, can stabilize the negative charge they acquire upon leaving, facilitating the reaction. Conversely, poor leaving groups can hinder the reaction, making it essential to evaluate the leaving group's strength when predicting the reaction pathway.