1. Propose multi-step syntheses to make the products shown below. Separate the steps with numbers. You should think about the product after each step you propose to make sure the scheme will work. Use the summary of reactions at the end of Ch 8,9, 10, 11, 17 to help you. Count the number of carbons in the reagents and products. A) Он .CI B) ??? HO, C) H2 ??? .CH3 CH3CCCH3 H3C° `CH3 Но

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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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**Task 1**: Propose multi-step syntheses to make the products shown below. Each step should be numbered, considering the product after each step to ensure the viability of the scheme. Reference the summary of reactions at the end of chapters 8, 9, 10, 11, and 17 for assistance. Count the number of carbons in both the reactants and the products.

**A) Reaction Pathway:**

- **Starting Material**: A six-carbon cycloalkane attached to a chlorine atom at the terminal position.
- **Product**: A six-carbon cycloalkane with an attached OH group at the same position as the chlorine in the starting material.

**B) Reaction Pathway:**

- **Starting Material**: A six-carbon cycloalkene with an ethyl group containing a triple bond.
- **Reaction**: Requires transformation to an eight-carbon cycloalkane with a carboxylic acid group (COOH) attached to an extended propyl chain.
- **Description**: Determine the series of reactions transforming the initial compound to the final carboxylic acid product.

**C) Reaction Pathway:**

- **Starting Material**: An alkyne, specifically 2-butyne (CH₃C≡CCH₃).
- **Product**: A three-carbon compound with an OH group and two methyl groups on the second carbon.
- **Description**: Ascertain the steps needed to achieve the product, ensuring correct placement of the OH group and methyl substituents.

Utilize the guidelines to construct detailed step-by-step reactions, ensuring all transformations preserve carbon count and functional group positioning.
Transcribed Image Text:**Task 1**: Propose multi-step syntheses to make the products shown below. Each step should be numbered, considering the product after each step to ensure the viability of the scheme. Reference the summary of reactions at the end of chapters 8, 9, 10, 11, and 17 for assistance. Count the number of carbons in both the reactants and the products. **A) Reaction Pathway:** - **Starting Material**: A six-carbon cycloalkane attached to a chlorine atom at the terminal position. - **Product**: A six-carbon cycloalkane with an attached OH group at the same position as the chlorine in the starting material. **B) Reaction Pathway:** - **Starting Material**: A six-carbon cycloalkene with an ethyl group containing a triple bond. - **Reaction**: Requires transformation to an eight-carbon cycloalkane with a carboxylic acid group (COOH) attached to an extended propyl chain. - **Description**: Determine the series of reactions transforming the initial compound to the final carboxylic acid product. **C) Reaction Pathway:** - **Starting Material**: An alkyne, specifically 2-butyne (CH₃C≡CCH₃). - **Product**: A three-carbon compound with an OH group and two methyl groups on the second carbon. - **Description**: Ascertain the steps needed to achieve the product, ensuring correct placement of the OH group and methyl substituents. Utilize the guidelines to construct detailed step-by-step reactions, ensuring all transformations preserve carbon count and functional group positioning.
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