**Problem 12: Oxidative Cleavage and Reaction Analysis**This problem involves the oxidative cleavage of an alkene using potassium permanganate (KMnO₄), resulting in the formation of two fragments. The alkene in question is compound J with the molecular formula C₈H₁₆. Upon cleavage, it yields butanoic acid and a ketone, Q.**Key Observations:**- **Alkene J (C₈H₁₆):** Undergoes oxidative cleavage.- **Products:** The identified fragments are butanoic acid and an unidentified ketone Q.- **Further Reaction:** When compound J reacts with one molar equivalent of hydrogen chloride (HCl), it forms an alkyl halide K with the formula C₈H₁₇Cl.**Objectives:**1. Determine the structures of J, J', and Q.2. Illustrate all involved reactions.3. Provide reasoning for the structural assignments.**Guidance for Problem Solving:**- **Structure Determination:** Analyze the given molecular formulas and deduce the potential structure for the alkene J based on its cleavage products.- **Reaction Mapping:** Illustrate the oxidative cleavage process and subsequent halogenation reactions.- **Reasoning:** Explain the step-by-step deductions leading to the structures of J, J', and Q.This problem integrates organic chemistry concepts such as oxidative cleavage of alkenes, functional group transformations, and halogenation reactions. Understanding these processes will aid in solving the structural and mechanistic elements of the task.

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Answered: 12.Use of KMnO4 to effect oxidative…

Chemistry

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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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