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In each reaction box, place the best reagent and conditions from the list. 1. CN H. 2. 3. Answer Bank NH, CH, CN NaBH,, CH, CH,OH Zn(Hg), HCl CH, NH, Br,. FeBr, PBr,, pyridine CH, MgBr NACN Mg. Et, O H,SO̟ H,, Pt NaNH,

In each reaction box, place the best reagent and conditions from the list. 1. CN H. 2. 3. Answer Bank NH, CH, CN NaBH,, CH, CH,OH Zn(Hg), HCl CH, NH, Br,. FeBr, PBr,, pyridine CH, MgBr NACN Mg. Et, O H,SO̟ H,, Pt NaNH,

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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### Chemical Reaction Problem In each reaction box, place the best reagent and conditions from the list provided in the Answer Bank. **Initial Reactant:** - Benzaldehyde structure with an aldehyde group (C=O at carbon 1 of benzene). **Final Product:** - Benzyl cyanide structure where the aldehyde group is replaced with a nitrile group (-CN). #### Reaction Steps: 1. **First Reaction Box:** 2. **Second Reaction Box:** 3. **Third Reaction Box:** ### Answer Bank Options: - \( \text{NH}_3 \) - \( \text{CH}_3\text{CN} \) - \( \text{NaBH}_4, \, \text{CH}_3\text{CH}_2\text{OH} \) - \( \text{Zn(Hg)}, \, \text{HCl} \) - \( \text{CH}_3\text{NH}_2 \) - \( \text{Br}_2, \, \text{FeBr}_3 \) - \( \text{PBr}_3, \, \text{pyridine} \) - \( \text{CH}_3\text{MgBr} \) - \( \text{NaCN} \) - \( \text{Mg, Et}_2\text{O} \) - \( \text{H}_2\text{SO}_4 \) - \( \text{H}_2, \, \text{Pt} \) - \( \text{NaNH}_2 \) ### Reaction Description You need to convert benzaldehyde to benzyl cyanide via three reaction steps by selecting the appropriate reagents from the answer bank.
Transcribed Image Text:### Chemical Reaction Problem In each reaction box, place the best reagent and conditions from the list provided in the Answer Bank. **Initial Reactant:** - Benzaldehyde structure with an aldehyde group (C=O at carbon 1 of benzene). **Final Product:** - Benzyl cyanide structure where the aldehyde group is replaced with a nitrile group (-CN). #### Reaction Steps: 1. **First Reaction Box:** 2. **Second Reaction Box:** 3. **Third Reaction Box:** ### Answer Bank Options: - \( \text{NH}_3 \) - \( \text{CH}_3\text{CN} \) - \( \text{NaBH}_4, \, \text{CH}_3\text{CH}_2\text{OH} \) - \( \text{Zn(Hg)}, \, \text{HCl} \) - \( \text{CH}_3\text{NH}_2 \) - \( \text{Br}_2, \, \text{FeBr}_3 \) - \( \text{PBr}_3, \, \text{pyridine} \) - \( \text{CH}_3\text{MgBr} \) - \( \text{NaCN} \) - \( \text{Mg, Et}_2\text{O} \) - \( \text{H}_2\text{SO}_4 \) - \( \text{H}_2, \, \text{Pt} \) - \( \text{NaNH}_2 \) ### Reaction Description You need to convert benzaldehyde to benzyl cyanide via three reaction steps by selecting the appropriate reagents from the answer bank.
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