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Suggest synthetic routes to each of the following form the indicated starting materials. You may use any other reagents. You can use other organic starting materials that is not explicitly excluded. However. all the carbons in the indicated starting materials have to end up in the final products. a. from as the only source ОН of carbon

Suggest synthetic routes to each of the following form the indicated starting materials. You may use any other reagents. You can use other organic starting materials that is not explicitly excluded. However. all the carbons in the indicated starting materials have to end up in the final products. a. from as the only source ОН of carbon

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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Suggest synthetic routes to each of the following form the indicated starting materials. You may use any other reagents. You can use other organic starting materials that is not explicitly excluded. However. all the carbons in the indicated starting materials have to end up in the final products.

**Transcription for Educational Website:** **Title: Synthetic Routes for Organic Compounds** **Introduction:** This document outlines synthetic routes for producing specified organic compounds using indicated starting materials. These synthetic exercises emphasize the use of creativity in selecting reagents while adhering to carbon atom constraints. **Instructions:** Suggest synthetic routes to each of the following compounds from the indicated starting materials. You may use any other reagents. You can use other organic starting materials that are not explicitly excluded. However, all the carbons in the indicated starting materials must end up in the final products. **Challenges:** **a.** - **Target Molecule:** An alcohol with the structure represented by a six-carbon chain with an -OH group attached to the second carbon from the left. - **Starting Material:** Propene. - **Condition:** Propene must be the only source of carbon in the synthesis. **b.** - **Target Molecule:** A carboxylic acid with the structure represented by a six-carbon chain with a -CO₂H group at the end. - **Starting Material:** A brominated alkane with the structure indicated. - **Condition:** Every carbon in the brominated alkane must be part of the final product. **c.** - **Target Molecule:** A benzylic alcohol containing deuterium (D) at specified positions. - **Starting Material:** An alcohol with the structure represented by a six-carbon chain containing specifically positioned deuterium (D) and hydrogen (H) atoms. - **Condition:** All carbons from the starting material must end in the final compound. The problems above encourage a deep understanding of organic synthesis strategies, ensuring adherence to carbon source constraints while exploring reaction mechanisms and pathways. Study and mastery of these transformations are crucial for developing proficiency in synthetic organic chemistry.
Transcribed Image Text:**Transcription for Educational Website:** **Title: Synthetic Routes for Organic Compounds** **Introduction:** This document outlines synthetic routes for producing specified organic compounds using indicated starting materials. These synthetic exercises emphasize the use of creativity in selecting reagents while adhering to carbon atom constraints. **Instructions:** Suggest synthetic routes to each of the following compounds from the indicated starting materials. You may use any other reagents. You can use other organic starting materials that are not explicitly excluded. However, all the carbons in the indicated starting materials must end up in the final products. **Challenges:** **a.** - **Target Molecule:** An alcohol with the structure represented by a six-carbon chain with an -OH group attached to the second carbon from the left. - **Starting Material:** Propene. - **Condition:** Propene must be the only source of carbon in the synthesis. **b.** - **Target Molecule:** A carboxylic acid with the structure represented by a six-carbon chain with a -CO₂H group at the end. - **Starting Material:** A brominated alkane with the structure indicated. - **Condition:** Every carbon in the brominated alkane must be part of the final product. **c.** - **Target Molecule:** A benzylic alcohol containing deuterium (D) at specified positions. - **Starting Material:** An alcohol with the structure represented by a six-carbon chain containing specifically positioned deuterium (D) and hydrogen (H) atoms. - **Condition:** All carbons from the starting material must end in the final compound. The problems above encourage a deep understanding of organic synthesis strategies, ensuring adherence to carbon source constraints while exploring reaction mechanisms and pathways. Study and mastery of these transformations are crucial for developing proficiency in synthetic organic chemistry.
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