Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts.

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**Title: Understanding SN1 Reactions in Organic Chemistry**

**Substitution Reaction Problem:**

**Question 8 of 22**

**Task:** Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts.

**Chemical Reaction:**

- **Reactant Structure:**
  - The main structure features a central carbon atom, which is bonded to:
    - A chlorine atom (Cl).
    - Two other carbon chains forming a tertiary carbon structure.
  - Below the structure is CH₃CO₂H, which is acetic acid, typically acting as a solvent or reagent in substitution reactions.

- **Arrow and Box:**
  - A downward arrow points to a dashed rectangle labeled "Draw SN1 Product," indicating where the major product of the reaction should be drawn.

**Instructions:**

- The goal is to determine the major organic product of the given SN1 reaction, considering the tertiary carbon structure and acetic acid context.
- Note that SN1 reactions typically involve the formation of a carbocation, where the leaving group (in this case, Cl) departs, resulting in a positively charged carbon ready to accept a nucleophile from the solvent or reagent.

**Explanation:**

In SN1 reactions, the major product generally arises from the nucleophile attacking the carbocation intermediate. Given the tertiary carbon, the reaction is likely to proceed through a stabilized carbocation, leading to a substitution product where the chlorine is replaced by the nucleophile provided by acetic acid.

Please use this understanding of SN1 reaction mechanisms to draw the correct substitution product in the provided space.
Transcribed Image Text:**Title: Understanding SN1 Reactions in Organic Chemistry** **Substitution Reaction Problem:** **Question 8 of 22** **Task:** Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts. **Chemical Reaction:** - **Reactant Structure:** - The main structure features a central carbon atom, which is bonded to: - A chlorine atom (Cl). - Two other carbon chains forming a tertiary carbon structure. - Below the structure is CH₃CO₂H, which is acetic acid, typically acting as a solvent or reagent in substitution reactions. - **Arrow and Box:** - A downward arrow points to a dashed rectangle labeled "Draw SN1 Product," indicating where the major product of the reaction should be drawn. **Instructions:** - The goal is to determine the major organic product of the given SN1 reaction, considering the tertiary carbon structure and acetic acid context. - Note that SN1 reactions typically involve the formation of a carbocation, where the leaving group (in this case, Cl) departs, resulting in a positively charged carbon ready to accept a nucleophile from the solvent or reagent. **Explanation:** In SN1 reactions, the major product generally arises from the nucleophile attacking the carbocation intermediate. Given the tertiary carbon, the reaction is likely to proceed through a stabilized carbocation, leading to a substitution product where the chlorine is replaced by the nucleophile provided by acetic acid. Please use this understanding of SN1 reaction mechanisms to draw the correct substitution product in the provided space.
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