Is charge stability greater in the products or in the reactants?

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter5: Resonance
Section: Chapter Questions
Problem 2CTQ: You will not find “hydroxide” in the stockroom, but you will find sodium hydroxide (NaOH)...
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Is charge stability greater in the products or in the reactants?

This image displays a chemical reaction scheme featuring two reactants.

**Reactant 1: Acetate Ion (CH₃COO⁻)**
- Structure: The acetate ion has a central carbon atom double-bonded to an oxygen atom (carbonyl group) and single-bonded to a methyl group (CH₃) and an oxygen with a negative charge.

**Reactant 2: Methyl Ethyl Sulfate (CH₃CH₂OSO₂OCH₃)**
- Structure: This molecule consists of an ethyl group (CH₃CH₂) connected to an oxygen atom, which is bonded to a sulfur atom. The sulfur atom is double-bonded to two oxygen atoms (forming the sulfonyl group). A methyl group (CH₃) is also attached via an oxygen.

**Reaction Arrow:**
- An arrow points towards the right, indicating the direction of the chemical reaction. The products are not shown in the image.

This scheme likely represents an organic chemical reaction where the acetate ion acts as a nucleophile, potentially involving nucleophilic substitution on the methyl group in methyl ethyl sulfate.
Transcribed Image Text:This image displays a chemical reaction scheme featuring two reactants. **Reactant 1: Acetate Ion (CH₃COO⁻)** - Structure: The acetate ion has a central carbon atom double-bonded to an oxygen atom (carbonyl group) and single-bonded to a methyl group (CH₃) and an oxygen with a negative charge. **Reactant 2: Methyl Ethyl Sulfate (CH₃CH₂OSO₂OCH₃)** - Structure: This molecule consists of an ethyl group (CH₃CH₂) connected to an oxygen atom, which is bonded to a sulfur atom. The sulfur atom is double-bonded to two oxygen atoms (forming the sulfonyl group). A methyl group (CH₃) is also attached via an oxygen. **Reaction Arrow:** - An arrow points towards the right, indicating the direction of the chemical reaction. The products are not shown in the image. This scheme likely represents an organic chemical reaction where the acetate ion acts as a nucleophile, potentially involving nucleophilic substitution on the methyl group in methyl ethyl sulfate.
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