1) Cњон Br + Mg(s) 2) Ho ether 1) 1) 2) Ho* 2) H3o*

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
The image presents a reaction scheme for an organic chemistry problem. 

**Instruction:**
3. Complete the following reaction scheme with the products.

**Reaction Details:**

- **Starting Materials:** 
  - A bromopropane compound reacts with magnesium metal (Mg) in the presence of an ether solvent.

- **First Reaction Pathway:**
  1. The reaction with the ether results in the formation of a Grignard reagent.
  2. This Grignard reagent reacts with formaldehyde followed by an acid workup (H₃O⁺) to potentially produce a primary alcohol.

- **Second Reaction Pathway:**
  1. Reaction with acetone followed by acid workup (H₃O⁺).
  2. This route is expected to yield a secondary alcohol.

- **Third Reaction Pathway:**
  1. Reaction with an ester, indicated by a carbonyl group and a methoxy group.
  2. Followed by acid workup (H₃O⁺), which likely results in the formation of a tertiary alcohol.

**Instruction:** 
Draw out these reactions, do not just draw structures for the products.

For an educational website, learners would draw the complete structures, including the transformation at each step, likely showcasing the progression from the Grignard reaction with carbonyl compounds to alcohol formation.
Transcribed Image Text:The image presents a reaction scheme for an organic chemistry problem. **Instruction:** 3. Complete the following reaction scheme with the products. **Reaction Details:** - **Starting Materials:** - A bromopropane compound reacts with magnesium metal (Mg) in the presence of an ether solvent. - **First Reaction Pathway:** 1. The reaction with the ether results in the formation of a Grignard reagent. 2. This Grignard reagent reacts with formaldehyde followed by an acid workup (H₃O⁺) to potentially produce a primary alcohol. - **Second Reaction Pathway:** 1. Reaction with acetone followed by acid workup (H₃O⁺). 2. This route is expected to yield a secondary alcohol. - **Third Reaction Pathway:** 1. Reaction with an ester, indicated by a carbonyl group and a methoxy group. 2. Followed by acid workup (H₃O⁺), which likely results in the formation of a tertiary alcohol. **Instruction:** Draw out these reactions, do not just draw structures for the products. For an educational website, learners would draw the complete structures, including the transformation at each step, likely showcasing the progression from the Grignard reaction with carbonyl compounds to alcohol formation.
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