Provide selective syntheses of both of the compounds below beginning with yl bromide. NO MECHANISMS! CI CH3 H Br Benzyl Bromide

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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Hello there!

Can you help me figure out selective synthesis for the second molecule please?

I have already completed the first molecule. I need to get to the second molecule from Benzyl Bromide using selective synthesis.

I am extremly lost at how to complete the second one, ive tried multiple times and I am stuck! Any help is appreciated!

Thank you so much!!

**Organic Chemistry Synthesis Problem**

**Objective:** 
Provide a selective synthesis of both compounds below, beginning with benzyl bromide. Note: NO MECHANISMS REQUIRED.

---

**Diagrams:**

1. **Compound 1:**
   - Starting from benzyl bromide (C₆H₅CH₂Br)
   - Reaction: Treat with NaCN
   - Product: Benzonitrile (C₆H₅CN)

2. **Compound 2:**
   - Starting from benzyl bromide (C₆H₅CH₂Br)
   - Reaction: Treat with aniline (NH₂)
   - Followed by: H₂ and Lindlar's catalyst
   - Product: Acetanilide (C₆H₅NHCOCH₃)

**Additional Notes:**
- The synthesis does not require detailed mechanisms.
- Focus is on the transformation of benzyl bromide to the desired products using provided reagents.
Transcribed Image Text:**Organic Chemistry Synthesis Problem** **Objective:** Provide a selective synthesis of both compounds below, beginning with benzyl bromide. Note: NO MECHANISMS REQUIRED. --- **Diagrams:** 1. **Compound 1:** - Starting from benzyl bromide (C₆H₅CH₂Br) - Reaction: Treat with NaCN - Product: Benzonitrile (C₆H₅CN) 2. **Compound 2:** - Starting from benzyl bromide (C₆H₅CH₂Br) - Reaction: Treat with aniline (NH₂) - Followed by: H₂ and Lindlar's catalyst - Product: Acetanilide (C₆H₅NHCOCH₃) **Additional Notes:** - The synthesis does not require detailed mechanisms. - Focus is on the transformation of benzyl bromide to the desired products using provided reagents.
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