Can someone Outline a chemical reaction for the formation of the compound and explain it and detail I really need to understand what is going on in the mechanism

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Can someone Outline a chemical reaction for the formation of the compound and explain it and detail I really need to understand what is going on in the mechanism 

**Introduction**

Oxidations are a very important class of reactions in organic chemistry. Most oxidations require either a heteroatom in a reduced state (oxygen in –OH, nitrogen in –NH₂, etc.) or a carbon-carbon π-bond (ozonolysis of alkenes and alkynes (and peroxide), the formation of oxiranes from alkenes using peroxy acids, etc.). The oxidation of an aromatic side chain does not require any of these factors. All that is needed is a benzylic carbon with at least one hydrogen attached to it. The oxidizing agents that can be used are chromic acid (using Na₂Cr₂O₇ or CrO₃ in sulfuric acid and water) or potassium permanganate (KMnO₄). The product in each case is benzoic acid or a derivative of benzoic acid (the permanganate reaction requires work up with acid because the permanganate reaction generates a basic solution as a byproduct):

**Chemical Reactions Illustrated**

1. A molecule with a methyl group (CH₃) attached to a benzene ring is oxidized using two different methods:

   - Using KMnO₄ and H₂O with heat, followed by H₃O⁺, H₂O; producing benzoic acid with COOH group attached to the benzene ring.

   - Using CrO₃, H₂SO₄, H₂O with heat; leading to a similar product where the methyl group is oxidized to a COOH group.

2. In a similar manner, a methyl group next to a NO₂ group on a benzene ring undergoes oxidation:

   - KMnO₄ and H₂O with heat, followed by H₃O⁺, H₂O; converting the methyl group into a COOH group.

   - Using CrO₃, H₂SO₄ and H₂O with heat; resulting in the same transformation of the methyl group to a COOH group.

**Experimental Example**

In the experiment, potassium permanganate is used to oxidize 2-chlorotoluene (o-chlorotoluene) to 2-chlorobenzoic acid (o-chlorobenzoic acid). Permanganate solutions are less hazardous than those containing chromium compounds, which are often carcinogenic.

**Chemical Reaction Depiction**

- 2-chlor
Transcribed Image Text:**Introduction** Oxidations are a very important class of reactions in organic chemistry. Most oxidations require either a heteroatom in a reduced state (oxygen in –OH, nitrogen in –NH₂, etc.) or a carbon-carbon π-bond (ozonolysis of alkenes and alkynes (and peroxide), the formation of oxiranes from alkenes using peroxy acids, etc.). The oxidation of an aromatic side chain does not require any of these factors. All that is needed is a benzylic carbon with at least one hydrogen attached to it. The oxidizing agents that can be used are chromic acid (using Na₂Cr₂O₇ or CrO₃ in sulfuric acid and water) or potassium permanganate (KMnO₄). The product in each case is benzoic acid or a derivative of benzoic acid (the permanganate reaction requires work up with acid because the permanganate reaction generates a basic solution as a byproduct): **Chemical Reactions Illustrated** 1. A molecule with a methyl group (CH₃) attached to a benzene ring is oxidized using two different methods: - Using KMnO₄ and H₂O with heat, followed by H₃O⁺, H₂O; producing benzoic acid with COOH group attached to the benzene ring. - Using CrO₃, H₂SO₄, H₂O with heat; leading to a similar product where the methyl group is oxidized to a COOH group. 2. In a similar manner, a methyl group next to a NO₂ group on a benzene ring undergoes oxidation: - KMnO₄ and H₂O with heat, followed by H₃O⁺, H₂O; converting the methyl group into a COOH group. - Using CrO₃, H₂SO₄ and H₂O with heat; resulting in the same transformation of the methyl group to a COOH group. **Experimental Example** In the experiment, potassium permanganate is used to oxidize 2-chlorotoluene (o-chlorotoluene) to 2-chlorobenzoic acid (o-chlorobenzoic acid). Permanganate solutions are less hazardous than those containing chromium compounds, which are often carcinogenic. **Chemical Reaction Depiction** - 2-chlor
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