### Reagents AvailableThis table lists various reagents that can be used in chemical reactions, specifically for transformations involving alcohols. Each reagent is labeled with a letter for easy reference.- **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)### InstructionsBelow the list of reagents, there are boxes where students can input their choices. These selections are intended for practicing the application of reagents to specific chemical reactions involving an alcohol starting material.- **Alcohol starting material:** [Box for input]- **Reagent for step 1:** [Box for input]- **Reagent for step 2:** [Box for input]- **Reagent for step 3:** [Box for input]Students should write the number/letters corresponding to the reagents they choose for each step of their proposed reaction sequence. This exercise helps to understand the practical applications of these reagents in organic chemistry. **Synthesis of Organic Compound with Bromine****Objective:** Identify the alcohol starting material and reagents needed for the synthesis of the shown compound with bromine.**Displayed Structure:** The image shows an organic compound with a bromine (Br) atom attached to a carbon chain.**Alcohol Starting Materials:** 1. Methanol2. Ethanol3. 1-Propanol4. 2-Propanol5. 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 selected for the synthesis in the boxes provided.1. **Alcohol Starting Material:** - Box to input choice2. **Reagent for Step 1:** - Box to input choice3. **Reagent for Step 2:** - Box to input choice4. **Reagent for Step 3:** - Box to input choice (if necessary)Note: If synthesis requires only two steps, enter "none" for step 3. **Navigation:** Options to go to the previous or next page are available at the bottom.

Answered: Image /qna-images/answer/8fcca12f-681b-4a56-a8b4-081c61c4691b.jpg

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. Br Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PB13 k. CH3 CH2 CH2 MgBr; then H3O+ b. H2 SO4 g. CrO3, H2SO4, H,O 1. Cg Hg M&B1 (phenylmagnesium bromide); then H3 O* с. НС h. NaH m. (CH3)2 CHMgBr: then H3O+ d. HBr i. CH3MGB1; then H30+ n. Dess-Martin periodinane (DMP) e. SOCI, j. CH3 CH2 MgBr; then H30+ Write the number/letters of the alchol/reagents in the boxes below. ( Previous Next

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. Br Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PB13 k. CH3 CH2 CH2 MgBr; then H3O+ b. H2 SO4 g. CrO3, H2SO4, H,O 1. Cg Hg M&B1 (phenylmagnesium bromide); then H3 O* с. НС h. NaH m. (CH3)2 CHMgBr: then H3O+ d. HBr i. CH3MGB1; then H30+ n. Dess-Martin periodinane (DMP) e. SOCI, j. CH3 CH2 MgBr; then H30+ Write the number/letters of the alchol/reagents in the boxes below. ( Previous Next

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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Question

### Reagents Available

This table lists various reagents that can be used in chemical reactions, specifically for transformations involving alcohols. Each reagent is labeled with a letter for easy reference.

- **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

Below the list of reagents, there are boxes where students can input their choices. These selections are intended for practicing the application of reagents to specific chemical reactions involving an alcohol starting material.

- **Alcohol starting material:** [Box for input]
- **Reagent for step 1:** [Box for input]
- **Reagent for step 2:** [Box for input]
- **Reagent for step 3:** [Box for input]

Students should write the number/letters corresponding to the reagents they choose for each step of their proposed reaction sequence. This exercise helps to understand the practical applications of these reagents in organic chemistry.

**Synthesis of Organic Compound with Bromine**

**Objective:**
Identify the alcohol starting material and reagents needed for the synthesis of the shown compound with bromine.

**Displayed Structure:**
The image shows an organic compound with a bromine (Br) atom attached to a carbon chain.

**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 selected for the synthesis in the boxes provided.

1. **Alcohol Starting Material:**
- Box to input choice

2. **Reagent for Step 1:**
- Box to input choice

3. **Reagent for Step 2:**
- Box to input choice

4. **Reagent for Step 3:**
- Box to input choice (if necessary)

Note: If synthesis requires only two steps, enter "none" for step 3.

**Navigation:**
Options to go to the previous or next page are available at the bottom.

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