Draw in the expected product below ### Predict the Product - Tutorial**Chemical Reaction Diagram Explanation:**The diagram provided depicts a chemical reaction involving a mogroside derivative, also known as Nectresse, which is an artificial sweetener. The reaction involves two steps:1. **Reagents**: - **TsCl, pyridine**: This step likely involves the conversion of an alcohol group into a tosylate, making it a better leaving group for subsequent reactions. 2. **Reagents**: - **NaSH, DMF**: This step involves the introduction of a nucleophilic substitution using sodium hydrosulfide in dimethylformamide.**Chemical Structure Details:**- The structure shown is a complex organic molecule with several ring systems and functional groups.- **Functional Groups**: Methoxy groups (OMe), hydroxyl groups (OH), and multiple chiral centers are present.**Expected Outcome:**The question mark indicates the need to predict the product formed after the two-step transformation involving the described reagents. The outcome should involve the substitution of the tosylated alcohol with the nucleophilic NaSH to form a new product with a thiol group.The educational exercise here likely focuses on understanding reaction mechanisms and predicting the stereochemistry and structure of the organic product formed through specific reagent interactions.

A question based on organic chemistry, which is to be accomplished.

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Draw in the expected product below

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter13: Alcohols, Phenols, And Ethers

Section: Chapter Questions

Problem 13.51E: Complete the following reactions: a. b. c.CH3SSCH2CH3+2(H)

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Draw in the expected product below

### Predict the Product - Tutorial

**Chemical Reaction Diagram Explanation:**

The diagram provided depicts a chemical reaction involving a mogroside derivative, also known as Nectresse, which is an artificial sweetener. The reaction involves two steps:

1. **Reagents**:
- **TsCl, pyridine**: This step likely involves the conversion of an alcohol group into a tosylate, making it a better leaving group for subsequent reactions.

2. **Reagents**:
- **NaSH, DMF**: This step involves the introduction of a nucleophilic substitution using sodium hydrosulfide in dimethylformamide.

**Chemical Structure Details:**

- The structure shown is a complex organic molecule with several ring systems and functional groups.
- **Functional Groups**: Methoxy groups (OMe), hydroxyl groups (OH), and multiple chiral centers are present.

**Expected Outcome:**

The question mark indicates the need to predict the product formed after the two-step transformation involving the described reagents. The outcome should involve the substitution of the tosylated alcohol with the nucleophilic NaSH to form a new product with a thiol group.

The educational exercise here likely focuses on understanding reaction mechanisms and predicting the stereochemistry and structure of the organic product formed through specific reagent interactions.

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