Specify the reagent you would use in each step of the following synthesis: a. LiAIH4 b. H₂SO4 c. HCI d. HBr e. SOCI2 step 1 step 2 Reagents Available j. CH3MgBr CI f. PBr3 k. CH3CH₂MgBr g. Dess-Martin periodinane (DMP) I. C6H5MgBr h. NaH i. NaOH (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3
Specify the reagent you would use in each step of the following synthesis: a. LiAIH4 b. H₂SO4 c. HCI d. HBr e. SOCI2 step 1 step 2 Reagents Available j. CH3MgBr CI f. PBr3 k. CH3CH₂MgBr g. Dess-Martin periodinane (DMP) I. C6H5MgBr h. NaH i. NaOH (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3
Chemistry
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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
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 Problem
**Objective:** Specify the reagent you would use in each step of the following synthesis.
#### Chemical Reaction Overview:
- **Starting Material:** A ketone with a methyl group (CH₃) and an ethyl group (CH₂CH₃) attached to the carbonyl carbon.
- **Step 1:** Converts the ketone to an intermediate.
- **Step 2:** The intermediate undergoes a chemical transformation to yield the final product, which contains a chlorine (Cl) atom and a phenyl group (C₆H₅) attached to the original carbon chain.
#### Reagents Available:
a. LiAlH₄
b. H₂SO₄
c. HCl
d. HBr
e. SOCl₂
f. PBr₃
g. Dess-Martin periodinane (DMP)
h. NaH
i. NaOH
j. CH₃MgBr
k. CH₃CH₂MgBr
l. C₆H₅MgBr (phenylmagnesium bromide)
m. (CH₃)₂CHMgBr
n. CrO₃
### Instructions:
- **Write the letters of the reagents in the boxes below.**
**Reagent for step 1:** [ ]
**Reagent for step 2:** [ ]
#### Explanation:
1. **Step 1** likely involves converting the ketone functional group using one of the reagents above.
2. **Step 2** involves introducing a chlorine atom and a phenyl group, suggesting the usage of a reagent capable of adding these specific functional groups.
Please select the appropriate reagents based on the chemical transformations needed for each step.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4f7442e5-ed1a-4154-ba5d-4813abad6cff%2Fff491cb9-da4c-49b5-8fce-8580dd157028%2Ft5erj9a_processed.png&w=3840&q=75)
Transcribed Image Text:### Synthesis Problem
**Objective:** Specify the reagent you would use in each step of the following synthesis.
#### Chemical Reaction Overview:
- **Starting Material:** A ketone with a methyl group (CH₃) and an ethyl group (CH₂CH₃) attached to the carbonyl carbon.
- **Step 1:** Converts the ketone to an intermediate.
- **Step 2:** The intermediate undergoes a chemical transformation to yield the final product, which contains a chlorine (Cl) atom and a phenyl group (C₆H₅) attached to the original carbon chain.
#### Reagents Available:
a. LiAlH₄
b. H₂SO₄
c. HCl
d. HBr
e. SOCl₂
f. PBr₃
g. Dess-Martin periodinane (DMP)
h. NaH
i. NaOH
j. CH₃MgBr
k. CH₃CH₂MgBr
l. C₆H₅MgBr (phenylmagnesium bromide)
m. (CH₃)₂CHMgBr
n. CrO₃
### Instructions:
- **Write the letters of the reagents in the boxes below.**
**Reagent for step 1:** [ ]
**Reagent for step 2:** [ ]
#### Explanation:
1. **Step 1** likely involves converting the ketone functional group using one of the reagents above.
2. **Step 2** involves introducing a chlorine atom and a phenyl group, suggesting the usage of a reagent capable of adding these specific functional groups.
Please select the appropriate reagents based on the chemical transformations needed for each step.
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