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3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 g. CrOs, H₂SO4, H₂O c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCI₂ j. CH₂ CH₂ MgBr; then H₂O+ Write the number/letters of the alchol/reagents the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Reagents available k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H₂O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)

3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 g. CrOs, H₂SO4, H₂O c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCI₂ j. CH₂ CH₂ MgBr; then H₂O+ Write the number/letters of the alchol/reagents the boxes below. Alcohol starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Reagents available k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H₂O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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### Synthesis of the Compound: Procedure and Materials To synthesize the compound shown in the diagram, follow these steps to specify both the alcohol starting material and the reagents you would use in each step. If the synthesis requires only two steps, enter "none" for step 3. #### Diagram of Target Compound ![Target Compound](diagram_url) ![Synthesis Reaction](diagram_url) #### Alcohol Starting Materials 1. **Methanol** 2. **Ethanol** 3. **1-Propanol** 4. **2-Propanol** 5. **Cyclohexanol** #### Reagents Available a. **LiAlH₄** b. **H₂SO₄** c. **HCl** d. **HBr** e. **SOCl₂** f. **PBr₃** g. **CrO₃, H₂SO₄, H₂O** h. **NaH** i. **CH₃MgBr; then H₃O⁺** j. **CH₃CH₂MgBr; then H₃O⁺** k. **CH₃CH₂CH₂MgBr; then H₃O⁺** l. **C₆H₅MgBr (phenylmagnesium bromide); then H₃O⁺** m. **(CH₃)₂CHMgBr; then H₃O⁺** n. **Dess-Martin periodinane (DMP)** #### Instructions Write the number/letters of the alcohol/reagents in the boxes below: | Field | Value | |----------------------------|-----------------| | Alcohol starting material | [Input Value] | | Reagent for step 1 | [Input Value] | | Reagent for step 2 | [Input Value] | | Reagent for step 3 | [Input Value] | To correctly input these values, analyze the chemical reactions and determine which reagents will properly convert the alcohol starting material into the desired product. ### Example Illustration If the target compound is synthesized from cyclohexanol (alcohol starting material) using LiAlH₄ (reagent), HCl (reagent), and then CrO₃, H₂SO₄, H₂O (reagent), you would enter: - Alcohol Starting Material: **5**
Transcribed Image Text:### Synthesis of the Compound: Procedure and Materials To synthesize the compound shown in the diagram, follow these steps to specify both the alcohol starting material and the reagents you would use in each step. If the synthesis requires only two steps, enter "none" for step 3. #### Diagram of Target Compound ![Target Compound](diagram_url) ![Synthesis Reaction](diagram_url) #### Alcohol Starting Materials 1. **Methanol** 2. **Ethanol** 3. **1-Propanol** 4. **2-Propanol** 5. **Cyclohexanol** #### Reagents Available a. **LiAlH₄** b. **H₂SO₄** c. **HCl** d. **HBr** e. **SOCl₂** f. **PBr₃** g. **CrO₃, H₂SO₄, H₂O** h. **NaH** i. **CH₃MgBr; then H₃O⁺** j. **CH₃CH₂MgBr; then H₃O⁺** k. **CH₃CH₂CH₂MgBr; then H₃O⁺** l. **C₆H₅MgBr (phenylmagnesium bromide); then H₃O⁺** m. **(CH₃)₂CHMgBr; then H₃O⁺** n. **Dess-Martin periodinane (DMP)** #### Instructions Write the number/letters of the alcohol/reagents in the boxes below: | Field | Value | |----------------------------|-----------------| | Alcohol starting material | [Input Value] | | Reagent for step 1 | [Input Value] | | Reagent for step 2 | [Input Value] | | Reagent for step 3 | [Input Value] | To correctly input these values, analyze the chemical reactions and determine which reagents will properly convert the alcohol starting material into the desired product. ### Example Illustration If the target compound is synthesized from cyclohexanol (alcohol starting material) using LiAlH₄ (reagent), HCl (reagent), and then CrO₃, H₂SO₄, H₂O (reagent), you would enter: - Alcohol Starting Material: **5**
**Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps, enter "none" for step 3.** [Drawing of the compound: 3-methyl-2-butanol] ### Alcohol Starting Materials 1. **methanol** 2. **ethanol** 3. **1-propanol** 4. **2-propanol** 5. **cyclohexanol** ### Reagents Available a. **LiAlH4** b. **H2SO4** c. **HCl** d. **HBr** e. **SOCl2** f. **PBr3** g. **CrO3, H2SO4, H2O** h. **NaH** i. **CH3MgBr; then H3O+** j. **CH3CH2MgBr; then H3O+** k. **CH3CH2CH2MgBr; then H3O+** l. **C6H5MgBr (phenylmagnesium bromide); then H3O+** m. **(CH3)2CHMgBr; then H3O+** n. **Dess-Martin periodinane (DMP)** ### Write the number/letters of the alcohol/reagents in the boxes below. - **Alcohol starting material:** [ ] - **Reagent for step 1:** [ ] - **Reagent for step 2:** [ ] - **Reagent for step 3:** [ ]
Transcribed Image Text:**Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps, enter "none" for step 3.** [Drawing of the compound: 3-methyl-2-butanol] ### Alcohol Starting Materials 1. **methanol** 2. **ethanol** 3. **1-propanol** 4. **2-propanol** 5. **cyclohexanol** ### Reagents Available a. **LiAlH4** b. **H2SO4** c. **HCl** d. **HBr** e. **SOCl2** f. **PBr3** g. **CrO3, H2SO4, H2O** h. **NaH** i. **CH3MgBr; then H3O+** j. **CH3CH2MgBr; then H3O+** k. **CH3CH2CH2MgBr; then H3O+** l. **C6H5MgBr (phenylmagnesium bromide); then H3O+** m. **(CH3)2CHMgBr; then H3O+** n. **Dess-Martin periodinane (DMP)** ### Write the number/letters of the alcohol/reagents in the boxes below. - **Alcohol starting material:** [ ] - **Reagent for step 1:** [ ] - **Reagent for step 2:** [ ] - **Reagent for step 3:** [ ]
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